BioMedLib Search Engine [ goto HOMEPAGE ]

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] Metastatic tumor of squamous cell carcinoma from uterine cervix to heart: ante-mortem diagnosis.

The pathological examination revealed metastasis of squamous cells with well-differentiated infiltrative areas.

Four months later, however, she was readmitted to hospital in terminal stage, confirming the guarded prognosis of the disease at this stage.

[MeSH-major] Carcinoma, Squamous Cell / secondary. Heart Neoplasms / secondary. Uterine Cervical Neoplasms / pathology

Genetic Alliance. consumer health - Carcinoma, Squamous Cell.

Genetic Alliance. consumer health - Heart tumor.

MedlinePlus Health Information. consumer health - Cervical Cancer.

International Agency for Research on Cancer - Screening Group. diagnostics - Histopathology and cytopathology of the uterine cervix - digital atlas .

International Agency for Research on Cancer - Screening Group. diagnostics - A practical manual on visual screening for cervical neoplasia .

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 17128293.001).

[ISSN] 1678-4170

[Journal-full-title] Arquivos brasileiros de cardiologia

[ISO-abbreviation] Arq. Bras. Cardiol.

[Language] eng; por

[Publication-type] Case Reports; Journal Article

[Publication-country] Brazil

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] Melanosis and squamous cell neoplasms of the upper aerodigestive tract in Japanese alcoholic men.

Melanosis is frequently observed in the upper aerodigestive tract of Japanese alcoholic men, and the prevalences of squamous cell dysplasia and SCC in the upper aerodigestive tract of Japanese alcoholic men are high.

This study evaluated associations between melanosis and both neoplasms of the upper aerodigestive tract and factors contributing to the development of melanosis in Japanese alcoholic men.

The presence of melanosis indicates a high risk for neoplasms in the upper aerodigestive tract of Japanese alcoholic men.

Melanosis and neoplasms have the same causes, including older age, heavy smoking, and high acetaldehyde exposure.

[MeSH-major] Alcoholism / complications. Carcinoma, Squamous Cell / epidemiology. Head and Neck Neoplasms / epidemiology. Melanosis / epidemiology. Respiratory System / pathology. Upper Gastrointestinal Tract / pathology

MedlinePlus Health Information. consumer health - Alcoholism and Alcohol Abuse.

MedlinePlus Health Information. consumer health - Head and Neck Cancer.

NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 16805853.001).

[ISSN] 1347-9032

[Journal-full-title] Cancer science

[ISO-abbreviation] Cancer Sci.

[Language] eng

[Publication-type] Journal Article; Research Support, Non-U.S. Gov't

[Publication-country] England

[Chemical-registry-number] EC 1.2.1.3 / ALDH2 protein, human; EC 1.2.1.3 / Aldehyde Dehydrogenase

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

Inverted papilloma (50%) was the commonest benign tumour and squamous cell carcinoma (36%) was the commonest malignancy.

[MeSH-major] Maxilla / surgery. Maxillary Sinus Neoplasms / surgery

[MeSH-minor] Adult. Carcinoma, Squamous Cell / surgery. Female. Humans. Male. Middle Aged. Papilloma, Inverted / surgery. Retrospective Studies

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 17240576.001).

[ISSN] 0300-5283

[Journal-full-title] The Medical journal of Malaysia

[ISO-abbreviation] Med. J. Malaysia

[Language] eng

[Publication-type] Journal Article

[Publication-country] Malaysia

   

Advertisement

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

Median rhomboid glossitis (MRG) is an uncommon benign abnormality of the tongue, most frequently affecting men.

This paper reports a case of rhomboid glossitis in a 61-year-old man who consulted for a painless raised lesion on the dorsum of the tongue, in left paramedial (not medial) location.

Other diagnoses considered but ruled out on the basis of the clinical and histopathological findings were haemangioma, pyogenic granuloma, amyloidosis, granular cell tumour, and squamous cell carcinoma.

[MeSH-minor] Amyloidosis / diagnosis. Antifungal Agents / therapeutic use. Candida albicans / isolation & purification. Candidiasis, Oral / diagnosis. Diagnosis, Differential. Granular Cell Tumor / diagnosis. Granuloma, Pyogenic / diagnosis. Hemangioma / diagnosis. Humans. Male. Middle Aged. Tongue Neoplasms / diagnosis

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 15735544.001).

[ISSN] 1698-6946

[Journal-full-title] Medicina oral, patología oral y cirugía bucal

[ISO-abbreviation] Med Oral Patol Oral Cir Bucal

[Language] eng; spa

[Publication-type] Case Reports; Journal Article

[Publication-country] Spain

[Chemical-registry-number] 0 / Antifungal Agents

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] Short term results of endoscopic submucosal dissection in superficial esophageal squamous cell neoplasms.

AIM: To evaluate the efficacy of endoscopic submucosal dissection for superficial esophageal squamous cell neoplasms.

METHODS: Between July 2007 and March 2009, 27 consecutive superficial esophageal squamous cell neoplasms in 25 enrolled patients were treated by endoscopic submucosal dissection.

The en block resection rate was 100% (27/27), and en block resection with tumor-free lateral/basal margins was 88.9% (24/27).

CONCLUSION: Endoscopic submucosal dissection is applicable to superficial esophageal squamous cell neoplasms with promising results.

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 21160693.001).

[ISSN] 1948-5190

[Journal-full-title] World journal of gastrointestinal endoscopy

[ISO-abbreviation] World J Gastrointest Endosc

[Language] eng

[Publication-type] Journal Article

[Publication-country] China

[Other-IDs] NLM/ PMC2999061

[Keywords] NOTNLM ; Endoscopic submucosal dissection / Endoscopy / Esophageal cancer / Neoplasm / Squamous cell

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] Comparative analysis of immunohistochemical markers with invasiveness and histologic differentiation in squamous cell carcinoma and basal cell carcinoma of the skin.

BACKGROUND: This study evaluates several tumor-related markers to examine the expression pattern of markers according to the invasiveness and histopathologic differentiation of squamous cell carcinoma and basal cell carcinoma.

METHODS: Ninety-four cases of squamous cell carcinoma and 108 cases of basal cell carcinoma using tissue array in order to determine correlations between the expression of Ki-67, p53, EGFR, CD44v6, MMP-1 and MMP-3, invasiveness and histologic differentiation.

RESULTS: The depth of invasion showed a correlation with CD44v6 expression of tumor cell in both squamous cell carcinoma and basal cell carcinoma (P = 0.009, P = 0.036, respectively) and with the MMP-1 expression of stromal cell in squamous cell carcinoma (P = 0.010).

The differentiation of squamous cell carcinoma was correlated with Ki-67 index.

The loss of palisading arrangement in basal cell carcinoma was correlated with the MMP-1 expression of stromal cells (P = 0.045).

CONCLUSIONS: CD44v6 and MMP-1, expressed in tumor cells and stromal cells respectively, are significant markers associated with the invasiveness of tumors in squamous cell carcinoma and basal cell carcinoma of the skin and that it will be helpful to evaluate the invasiveness by measuring the expression of these markers.

[MeSH-major] Biomarkers, Tumor / biosynthesis. Carcinoma, Basal Cell / pathology. Carcinoma, Squamous Cell / pathology. Skin Neoplasms / pathology

[MeSH-minor] Adult. Aged. Aged, 80 and over. Antigens, CD44 / biosynthesis. Female. Genes, erbB-1. Humans. Immunohistochemistry. Ki-67 Antigen / biosynthesis. Male. Matrix Metalloproteinase 1 / biosynthesis. Matrix Metalloproteinase 3 / biosynthesis. Middle Aged. Neoplasm Invasiveness. Tumor Suppressor Protein p53 / biosynthesis

Genetic Alliance. consumer health - Carcinoma, Squamous Cell.

MedlinePlus Health Information. consumer health - Skin Cancer.

NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .

NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .

NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .

NCI CPTC Antibody Characterization Program. NCI CPTC Antibody Characterization Program .

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 18404670.001).

[ISSN] 0022-4790

[Journal-full-title] Journal of surgical oncology

[ISO-abbreviation] J Surg Oncol

[Language] eng

[Publication-type] Comparative Study; Journal Article

[Publication-country] United States

[Chemical-registry-number] 0 / Antigens, CD44; 0 / Biomarkers, Tumor; 0 / CD44 protein, human; 0 / Ki-67 Antigen; 0 / Tumor Suppressor Protein p53; EC 3.4.24.17 / Matrix Metalloproteinase 3; EC 3.4.24.7 / Matrix Metalloproteinase 1

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

The investigation involved 285 patients suffering from recurrences and distant metastases of uterine carcinoma cases of 24% of all (primary tumor).

Local recurrence rate for primary squamous cell tumor was 53.6%, adenocarcinoma - 6.3% and poorly-differentiated cell carcinoma - 4.9%.

[MeSH-major] Carcinoma / secondary. Carcinoma / therapy. Neoplasm Recurrence, Local / therapy. Uterine Cervical Neoplasms / pathology. Uterine Cervical Neoplasms / therapy

[MeSH-minor] Adenocarcinoma / secondary. Adenocarcinoma / therapy. Adult. Carcinoma, Squamous Cell / secondary. Carcinoma, Squamous Cell / therapy. Chemotherapy, Adjuvant. Female. Humans. Intestinal Neoplasms / secondary. Intestinal Neoplasms / therapy. Lymphatic Metastasis. Middle Aged. Neoplasm Invasiveness. Radiotherapy, Adjuvant. Retrospective Studies. Treatment Outcome. Urologic Neoplasms / secondary. Urologic Neoplasms / therapy

MedlinePlus Health Information. consumer health - Cervical Cancer.

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 19670732.001).

[ISSN] 0507-3758

[Journal-full-title] Voprosy onkologii

[ISO-abbreviation] Vopr Onkol

[Language] rus

[Publication-type] English Abstract; Journal Article

[Publication-country] Russia (Federation)

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] [Expression pattern of MAL in normal epithelial cells, benign tumor, and squamous cell carcinoma of larynx].

METHOD: Use the immunohistochemical technique to analyze the distribution of MAL in normal laryngeal epithelial cells, polyp of vocal cords, laryngeal atypical hyperplasia and laryngeal squamous cell carcinoma.

Comparatively, MAL expression is significantly down regulated in laryngeal atypical hyperplasia and laryngeal squamous cell carcinomas (P < 0.05).

MAL, therefore, is a potential marker for early diagnosis of laryngeal squamous cell carcinoma.

[MeSH-major] Carcinoma, Squamous Cell / metabolism. Laryngeal Mucosa / metabolism. Laryngeal Neoplasms / metabolism. Membrane Transport Proteins / metabolism. Myelin Proteins / metabolism. Proteolipids / metabolism

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 19670627.001).

[ISSN] 1001-1781

[Journal-full-title] Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery

[ISO-abbreviation] Lin Chung Er Bi Yan Hou Tou Jing Wai Ke Za Zhi

[Language] chi

[Publication-type] English Abstract; Journal Article

[Publication-country] China

[Chemical-registry-number] 0 / MAL protein, human; 0 / Membrane Transport Proteins; 0 / Myelin Proteins; 0 / Myelin and Lymphocyte-Associated Proteolipid Proteins; 0 / Proteolipids

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

RESULTS: The 38 unusual malignancies metastasizing to the pleural cavity included 29 haematological malignancies (non-Hodgkin's lymphoma, acute lymphoid leukaemia, multiple myeloma and chronic myeloid leukaemia) and nine non-haematological malignancies (Ewing's sarcoma, neuroblastoma, Wilms' tumour, squamous cell carcinoma, small-cell carcinoma and malignant fibrous histiocytoma).

[MeSH-major] Neoplasms / pathology. Pleural Effusion, Malignant / pathology

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 17250600.001).

[ISSN] 0956-5507

[Journal-full-title] Cytopathology : official journal of the British Society for Clinical Cytology

[ISO-abbreviation] Cytopathology

[Language] eng

[Publication-type] Journal Article

[Publication-country] England

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] Markers of squamous cell carcinoma in sarco/endoplasmic reticulum Ca2+ ATPase 2 heterozygote mice keratinocytes.

A mutation of Atp2a2 gene encoding the sarco/endoplasmic reticulum Ca(2+)-ATPase 2 (SERCA2) causes Darier's disease in human and null mutation in one copy of Atp2a2 leads to a high incidence of squamous cell tumor in a mouse model.

In SERCA2 heterozygote (SERCA2(+/-)) mice keratinocytes, mechanisms involved in partial depletion of SERCA2 gene and its related tumor induction have not been studied.

Using the gene fishing system, we first found in SERCA2(+/-) keratinocytes that gene level of tumor-associated calcium signal transducer 1, crystalline alphaB, procollagen XVIII alpha1, and nuclear factor I-B were increased.

These results suggest that the alterations of Ca(2+) signaling by SERCA2 haploinsufficiency alternate the gene expression of tumor induction and differentiation in keratinocytes.

[MeSH-major] Carcinoma, Squamous Cell / metabolism. Heterozygote. Keratinocytes / metabolism. Sarcoplasmic Reticulum Calcium-Transporting ATPases / genetics. Sarcoplasmic Reticulum Calcium-Transporting ATPases / metabolism

Genetic Alliance. consumer health - Carcinoma, Squamous Cell.

COS Scholar Universe. author profiles.

NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .

NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .

[Email] Email this result item

Email the results to the following email address:   [X] Close

[Copyright] Crown Copyright 2009. Published by Elsevier Ltd. All rights reserved.

(PMID = 19840814.001).

[ISSN] 1873-1732

[Journal-full-title] Progress in biophysics and molecular biology

[ISO-abbreviation] Prog. Biophys. Mol. Biol.

[Language] eng

[Publication-type] Journal Article; Research Support, Non-U.S. Gov't; Review

[Publication-country] England

[Chemical-registry-number] 0 / Biomarkers; EC 3.6.3.8 / Sarcoplasmic Reticulum Calcium-Transporting ATPases

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

: 8091 Background: Signaling of Insulin like Growth Factors (IGFs) through the IGF type 1 receptor (IGF-IR) induces tumor resistance to cancer therapy.

Figitumumab (F) (CP-751,871), a specific IGF-IR inhibitor, has shown phase 2 activity in NSCLC in some histologies (i.e., squamous cell and adenocarcinoma) but not others (i.e, large cell or NOS tumors).

Gene expression profiling was conducted in 35 NSCLC cell lines treated with F.

RESULTS: Squamous NSCLC had the highest IGF-IR expression (p=0.057).

This subset included 73% of the squamous cell tumors investigated (N=44).

Plasma levels of free IGF-1 (fIGF-1) were low and not predictive of response in squamous cell.

Large cell/NOS NSCLC expressed the highest levels of vimentin (p<0.001) but had low E-cadherin and IGF-IR expression and low fIGF-1 plasma levels.

Analysis of anchorage independent growth in NSCLC cell lines confirmed that F activity is independently associated to IGF-IR overexpression (p=0.02) and IGFBP3 under-expression (p=0.009).

CONCLUSIONS: IGF-IR overexpression and increased free IGFs/low IGFBP are key independent mechanisms of sensitivity to F in NSCLC of squamous and adenocarcinoma cell histologies.

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 27962669.001).

[ISSN] 1527-7755

[Journal-full-title] Journal of clinical oncology : official journal of the American Society of Clinical Oncology

[ISO-abbreviation] J. Clin. Oncol.

[Language] eng

[Publication-type] Journal Article

[Publication-country] United States

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] Correlation between FDG PET/CT and the expression of Ki-67, MMP-2, micro-vessel density (MVD), and pathological grading in squamous cell carcinoma of the esophagus.

: e15556 Background: Variable uptake of 18FDG has been noticed in positron emission tomography (PET) studies of patients with esophageal squamous cell carcinoma (ESCC).

The aim of the present study was to determine if ¹⁸F-FDG PET/CT standardized uptake value (SUV) could quantitatively reflect tumor proliferation, invasion and angiogenesis, and to reveal the relationship between SUV and pathological grading of ESCC.

18FDG uptake was semiquantitatively measured by SUV.Tumour sections were HE stained to determine the pathological grading,and were stained by immunohistochemistry for proliferation marker (Ki67), invasion marker (MMP-2), and angiogenic marker (CD34).

RESULTS: Among all the 47 cases,there were 13 well- differentiated squamous cell tumors, 16 moderately differentiated tumors and 18 poorly differentiated tumors,45 of 47 tumors revealed FDG. accumulation in primary tumor foci confirmed by subsequently histopathologically.

The mean FDG SUVmax value was 12.504 ± 6.805.

The SUV and Ki-67 index, MMP-2 index were positively correlated (r=0.581,0.594), and it was not correlated with MVD(P>0.05).

The mean SUV of well-differentiated, moderately differentiated and poorly differentiated tumors were 9.787±1.477, 12.313±0.479, 15.053±2.147 respectively, and a significant difference could be determined between them by statistical analysis(P=0.000).

SUV could reflect proliferation and invasion potential of tumor.

However, there is no significant correlation between SUV and MVD, thus it could not reflect tumor angiogenesis in ESCC.

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 27962337.001).

[ISSN] 1527-7755

[Journal-full-title] Journal of clinical oncology : official journal of the American Society of Clinical Oncology

[ISO-abbreviation] J. Clin. Oncol.

[Language] eng

[Publication-type] Journal Article

[Publication-country] United States

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

The aim of this study was to determine the number of cases of laryngeal cancer seen at the Korle Bu Teaching Hospital, establish epidemiological parameters of the disease and to outline preventive measures.

METHOD: One hundred and fifteen (115) patients who were managed for laryngeal cancer from 1(st) January 1998 to 31(st) December 2003 were studied retrospectively with respect to age, sex, duration of symptoms at presentation, risk factors, symptoms complex, histopathology, stage of tumor, details of treatment offered and follow up.

A significant proportion of cases (37.3%) presented with locally advanced disease.

The commonest histological type of laryngeal tumour seen was squamous cell carcinoma.

Only 58 (69.9%) patients completed radiotherapy treatment and in all 32 (24.3 %) patients did not report for any treatment.

CONCLUSIONS: We conclude that significant number of patients with laryngeal cancer presented with locally advanced disease and dysphonia was the commonest symptom.

[Email] Email this result item

Email the results to the following email address:   [X] Close

[Cites] Laryngoscope. 1975 Jul;85(7):1190-6 [1152568.001]

[Cites] Int J Radiat Oncol Biol Phys. 1991 Jan;20(1):21-8 [1993628.001]

[Cites] Am J Surg. 1991 Oct;162(4):337-40 [1951884.001]

(PMID = 17299565.001).

[ISSN] 0016-9560

[Journal-full-title] Ghana medical journal

[ISO-abbreviation] Ghana Med J

[Language] eng

[Publication-type] Journal Article

[Publication-country] Ghana

[Other-IDs] NLM/ PMC1790844

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

The aim of this study was to assess the usefulness of fine needle aspiration cytology (FNAC) as a diagnostic method in lung tumour as well as to determine the incidence of lung cancer in various age and sex group and in relation with smoking.

The most common tumour was squamous cell carcinoma (45%) followed by adenocarcinoma (22%), small cell carcinoma (16%) and large cell carcinoma (8%).

[MeSH-major] Biopsy, Fine-Needle. Lung Neoplasms / diagnosis

[MeSH-minor] Adenocarcinoma / diagnosis. Adenocarcinoma / epidemiology. Adult. Age Factors. Aged. Aged, 80 and over. Carcinoma, Large Cell / diagnosis. Carcinoma, Large Cell / epidemiology. Carcinoma, Small Cell / diagnosis. Carcinoma, Small Cell / epidemiology. Carcinoma, Squamous Cell / diagnosis. Carcinoma, Squamous Cell / epidemiology. Cytodiagnosis. Female. Histocytochemistry. Humans. Male. Middle Aged. Predictive Value of Tests. Risk Factors. Smoking

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 17474260.001).

[ISSN] 0377-4929

[Journal-full-title] Indian journal of pathology & microbiology

[ISO-abbreviation] Indian J Pathol Microbiol

[Language] eng

[Publication-type] Journal Article

[Publication-country] India

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] Topical application of representative multifunctional acrylates produced proliferative and inflammatory lesions in F344/N rats and B6C3F1 mice, and squamous cell neoplasms in Tg.AC mice.

Topical application of TMPTA and PETA to Tg.AC mice showed dose-dependent increases in squamous cell papillomas at the site of application, with decreases in the latency of their appearance in mice receiving 3 mg/kg or greater.

Papillomas, the reporter phenotype in Tg.AC mice, were accompanied by a few squamous cell carcinomas, along with hyperplastic and inflammatory lesions.

[MeSH-major] Acrylates / toxicity. Papilloma / chemically induced. Precancerous Conditions / chemically induced. Propylene Glycols / toxicity. Skin Neoplasms / chemically induced. Stomach Neoplasms / chemically induced

MedlinePlus Health Information. consumer health - Skin Cancer.

MedlinePlus Health Information. consumer health - Stomach Cancer.

Hazardous Substances Data Bank. Trimethylolpropane triacrylate .

KOMP Repository. gene/protein/disease-specific - KOMP Repository (subscription/membership/fee required).

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 16176922.001).

[ISSN] 0192-6233

[Journal-full-title] Toxicologic pathology

[ISO-abbreviation] Toxicol Pathol

[Language] eng

[Publication-type] Journal Article

[Publication-country] United States

[Chemical-registry-number] 0 / Acrylates; 0 / Propylene Glycols; 4B67KGL96S / trimethylolpropane triacrylate; PJJ1161ULF / pentaerythrityl triacrylate

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] Squamous cell carcinoma of the lip after allogeneic hemopoietic stem cell transplantation.

Allogeneic hemopoietic stem cell transplantation (HSCT) has been considered a curative treatment option for many hematological and non-hematological disorders.

Despite the use of advanced methods of tissue typing and new therapies, graft versus host disease (GVHD) remains a major obstacle.

Secondary malignancies are also among the most serious long-term complications after HSCT including leukemia, lymphomas, and to a lesser extent, solid tumors.

The most commonly observed solid tumor is squamous cell carcinoma (SCC).

[MeSH-major] Carcinoma, Squamous Cell / pathology. Carcinoma, Squamous Cell / surgery. Hematopoietic Stem Cell Transplantation. Lip Neoplasms / pathology. Lip Neoplasms / surgery. Neoplasms, Second Primary / pathology. Neoplasms, Second Primary / surgery

[MeSH-minor] Adult. Graft vs Host Disease / pathology. Graft vs Host Disease / surgery. Humans. Leukemia, Myelogenous, Chronic, BCR-ABL Positive / pathology. Leukemia, Myelogenous, Chronic, BCR-ABL Positive / therapy. Male. Multiple Myeloma / pathology. Multiple Myeloma / therapy. Transplantation, Homologous

Genetic Alliance. consumer health - Carcinoma, Squamous Cell.

Genetic Alliance. consumer health - Transplantation.

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 20543542.001).

[ISSN] 1658-3876

[Journal-full-title] Hematology/oncology and stem cell therapy

[ISO-abbreviation] Hematol Oncol Stem Cell Ther

[Language] eng

[Publication-type] Case Reports; Journal Article

[Publication-country] Saudi Arabia

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

The cytotoxic activities of these compounds were evaluated against human nasopharyngeal epidermoid tumor cell line KB, and compounds 1 and 8-11 showed strong anticancer activities in vitro, comparable with that of 5-fluorouracil, an anticancer drug.

[MeSH-minor] Antineoplastic Agents, Phytogenic / chemical synthesis. Antineoplastic Agents, Phytogenic / chemistry. Antineoplastic Agents, Phytogenic / pharmacology. Cell Survival / drug effects. Drug Screening Assays, Antitumor. Humans. KB Cells. Molecular Structure. Stereoisomerism. Structure-Activity Relationship

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 17193329.001).

[ISSN] 1612-1880

[Journal-full-title] Chemistry & biodiversity

[ISO-abbreviation] Chem. Biodivers.

[Language] eng

[Publication-type] Journal Article; Research Support, Non-U.S. Gov't

[Publication-country] Switzerland

[Chemical-registry-number] 0 / Antineoplastic Agents, Phytogenic; 0 / Stilbenes; Q369O8926L / resveratrol

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] Esophageal melanosis, an endoscopic finding associated with squamous cell neoplasms of the upper aerodigestive tract, and inactive aldehyde dehydrogenase-2 in alcoholic Japanese men.

BACKGROUND: Esophageal melanosis is often observed in alcoholic Japanese men, in whom the prevalence of squamous cell dysplasia and carcinoma (SCC) in the upper aerodigestive tract are high.

This study evaluated the associations of esophageal melanosis with these neoplasms, and the factors contributing to the development of esophageal melanosis in this population.

[MeSH-major] Alcoholism / complications. Aldehyde Dehydrogenase / metabolism. Carcinoma, Squamous Cell / diagnosis. Esophageal Neoplasms / diagnosis. Melanosis / pathology. Precancerous Conditions / pathology

[MeSH-minor] Adult. Age Distribution. Aged. Aldehyde Dehydrogenase, Mitochondrial. Biomarkers, Tumor / analysis. Biomarkers, Tumor / metabolism. Biopsy, Needle. Confidence Intervals. Digestive System Neoplasms / diagnosis. Digestive System Neoplasms / epidemiology. Esophagoscopy / methods. Genotype. Humans. Immunohistochemistry. Incidence. Japan / epidemiology. Male. Mass Screening / methods. Middle Aged. Odds Ratio. Risk Assessment. Survival Analysis

MedlinePlus Health Information. consumer health - Alcoholism and Alcohol Abuse.

MedlinePlus Health Information. consumer health - Esophageal Cancer.

NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .

[Email] Email this result item

Email the results to the following email address:   [X] Close

[Cites] Exp Dermatol. 1999 Apr;8(2):153-64 [10232409.001]

[Cites] J Invest Dermatol. 1989 Apr;92(4):565-72 [2467948.001]

[Cites] Carcinogenesis. 1997 Sep;18(9):1739-43 [9328169.001]

[Cites] Am J Dermatopathol. 1998 Aug;20(4):357-61 [9700373.001]

[Cites] J Eur Acad Dermatol Venereol. 2000 Nov;14(6):448-65 [11444266.001]

[Cites] Cancer. 1963 Jan;16:48-50 [14025842.001]

[Cites] Alcohol Clin Exp Res. 1993 Apr;17(2):376-81 [8488982.001]

[Cites] Carcinogenesis. 2002 Nov;23 (11):1851-9 [12419833.001]

[Cites] Arch Pathol. 1974 Aug;98(2):87-9 [4134908.001]

[Cites] Cancer. 1995 Sep 15;76(6):928-34 [8625217.001]

[Cites] Alcohol Clin Exp Res. 1997 Sep;21(6):1073-82 [9309320.001]

[Cites] Arch Environ Health. 1983 Nov-Dec;38(6):375-8 [6667039.001]

[Cites] Dis Esophagus. 2002;15(3):244-9 [12444999.001]

[Cites] Alcohol Clin Exp Res. 1991 Feb;15(1):141-4 [2024727.001]

[Cites] Gastroenterology. 1991 Jan;100(1):13-6 [1983815.001]

[Cites] Virchows Arch A Pathol Anat Histopathol. 1990;417(2):137-43 [2114692.001]

[Cites] Alcohol Clin Exp Res. 2001 May;25(5 Suppl ISBRA):15S-32S [11391045.001]

[Cites] Am J Gastroenterol. 1989 Dec;84(12):1475-81 [2688398.001]

[Cites] Alcohol Alcohol Suppl. 1993;1A:11-3 [8141918.001]

[Cites] Ann Pathol. 1989;9(1):57-61 [2712872.001]

[Cites] J Natl Cancer Inst. 1997 Nov 19;89(22):1692-7 [9390538.001]

[Cites] Jpn J Clin Oncol. 2003 Mar;33(3):111-21 [12672787.001]

[Cites] Am J Psychiatry. 1995 Aug;152(8):1219-21 [7625477.001]

[Cites] J Oral Pathol Med. 1991 Jan;20(1):8-12 [2002444.001]

[Cites] Gut. 2000 Aug;47(2):256-61 [10896918.001]

[Cites] Endoscopy. 1990 Mar;22(2):94-5 [2335153.001]

[Cites] Virchows Arch A Pathol Anat Histopathol. 1991;418(6):515-22 [2058085.001]

[Cites] Histopathology. 1997 May;30(5):498-9 [9181376.001]

[Cites] Int J Cancer. 1996 Nov 4;68(3):313-6 [8903472.001]

[Cites] Gan. 1965 Apr;56:177-87 [14321932.001]

[Cites] J Natl Cancer Inst. 1993 Dec 15;85(24):2030-3 [8246289.001]

[Cites] Carcinogenesis. 2001 Mar;22(3):433-9 [11238183.001]

(PMID = 16082583.001).

[ISSN] 0944-1174

[Journal-full-title] Journal of gastroenterology

[ISO-abbreviation] J. Gastroenterol.

[Language] eng

[Publication-type] Comparative Study; Journal Article; Research Support, Non-U.S. Gov't

[Publication-country] Japan

[Chemical-registry-number] 0 / Biomarkers, Tumor; EC 1.2.1.3 / ALDH2 protein, human; EC 1.2.1.3 / Aldehyde Dehydrogenase; EC 1.2.1.3 / Aldehyde Dehydrogenase, Mitochondrial

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] Radiotherapy treatment delays and their influence on tumour control achieved by various fractionation schedules.

There is often a considerable delay from initial tumour diagnosis to the start of radiotherapy treatment.

This paper extends the calculations of a previous paper on the effects of delays before the initiation of radiotherapy treatment to include results from a variety of practical fractionation regimes for three different types of tumour: squamous cell carcinoma (head and neck), breast and prostate.

The linear quadratic model of radiation effect, logarithmic tumour growth (coupled with delay times where relevant) and the Poisson model for tumour control probability (TCP) are used to calculate the change in TCP for delays between diagnosis and treatment.

The results show that delays in the start of radiotherapy treatment do have an adverse effect on tumour control for fast-growing tumours.

For example, calculations predict a reduction in local tumour control of up to 1.5% per week's delay for head and neck cancers treated following surgery.

In addition, there may be a variety of fractionation regimes that will yield very similar clinical results for each tumour type.

It is shown theoretically that, for the tumour types considered here, it is possible to increase the dose per fraction and decrease the number of fractions while maintaining or increasing TCP relative to standard 2 Gy fractionation regimes, although there may be some advantage to using hyperfractionated regimes for head and neck cancers in order to reduce normal tissue effects.

[MeSH-major] Breast Neoplasms / radiotherapy. Head and Neck Neoplasms / radiotherapy. Prostatic Neoplasms / radiotherapy

MedlinePlus Health Information. consumer health - Breast Cancer.

MedlinePlus Health Information. consumer health - Head and Neck Cancer.

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 18378526.001).

[ISSN] 1748-880X

[Journal-full-title] The British journal of radiology

[ISO-abbreviation] Br J Radiol

[Language] eng

[Publication-type] Journal Article

[Publication-country] England

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] An overview of Bcl-2 expression in histopathological variants of basal cell carcinoma, squamous cell carcinoma, actinic keratosis and seborrheic keratosis.

The Bcl-2 protein has been shown to suppress cell death and protects cell against apoptosis induced by different death-inducing signals.

In this study the authors have analyzed imunohistochemically the expression of Bcl-2 protein in the histopathological variants of the most common malignant tumors of the skin--basal cell carcinoma (BCC) and squamous cell tumor (SCC), as well as in the precancerous lesion actinic keratosis (AK) and in benign tumor seborrheic keratosis (SK).

Bcl-2 expression in solid, adenoid and cystic variants of BCC exhibited immunoreactivity of tumor stroma with more intense staining among peripheral palisading cells.

Among SCC in all samples, tumor tissue lack to express Bcl-2 positivity.

In cases of hypertrophic and atrophic variants of AK, Bcl-2 expression was confined to basal cell layer, as well as in one case of hypertrophic variant in suprabasal cells.

In three histological variants of SK expresseion of Bcl-2 protein was in areas of basaloid proliferation, while in areas of squamous differentiation was negative.

In clonal variant immunostaining was positive among cells in characteristic "nests" Distribution of Bcl-2 protein expression in solid, adenoid and cystic variant of BCC showed that peripheral proliferating cells are protected against apoptosis what permits tumor growth.

In morpheaform variant reduced amount of Bcl-2 expression indicated that this variant of BCC has increased cell proliferation, and in practice shows tendency for recurrence and difficulties to eradicate.

Bcl-2 expression supports the observation that tumor cells are derived from basal keratinocytes.

In SCC, lack of Bcl-2 expression indicates that origin of tumor cells is from more differentiated suprabasal keratinocytes.

In AK results suggest that immunoreactivity is regulated with respect of the keratinocyte's differentiation status, but not closely correlate with proliferative rate.

[MeSH-major] Carcinoma, Basal Cell / metabolism. Carcinoma, Squamous Cell / metabolism. Keratosis, Actinic / metabolism. Keratosis, Seborrheic / metabolism. Proto-Oncogene Proteins c-bcl-2 / metabolism. Skin Neoplasms / metabolism

Genetic Alliance. consumer health - Carcinoma, Squamous Cell.

Genetic Alliance. consumer health - Keratosis, seborrheic.

MedlinePlus Health Information. consumer health - Skin Cancer.

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 19138009.001).

[ISSN] 0350-6134

[Journal-full-title] Collegium antropologicum

[ISO-abbreviation] Coll Antropol

[Language] eng

[Publication-type] Journal Article

[Publication-country] Croatia

[Chemical-registry-number] 0 / Proto-Oncogene Proteins c-bcl-2

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] A colliding maxillary sinus cancer of adenosquamous carcinoma and small cell neuroendocrine carcinoma--a case report with EGFR copy number analysis.

BACKGROUND: Small cell neuroendocrine carcinoma (SNEC) of maxillary sinus is a rare and aggressive malignancy.

A tumor with squamous cell carcinoma, adenocarcinoma and SNEC co-existence is extremely rare.

CASE PRESENTATION: We present a colliding tumor of squamous cell, adenocarcinoma and SNEC in maxillary sinus.

Magnetic resonance imaging showed a tumor involving left maxilla and orbital floor.

Excision of tumor was done and the defect was reconstructed with free flap.

The pathology revealed a malignant tumor composed of squamous cell carcinoma, adenocarcinoma and SNEC components.

EGFR FISH study showed no gene amplification in 3 components of this tumor.

The tumor progressed rapidly and the patient expired at 8 months after surgery.

CONCLUSION: A colliding tumor of squamous cell, adenocarcinoma and neuroendocrine carcinoma in maxillary sinus was aggressive in behavior and the treatment response was poor due to the complexity of tumor.

[MeSH-major] Carcinoma, Neuroendocrine / genetics. Carcinoma, Small Cell / genetics. DNA, Neoplasm / genetics. Maxillary Sinus Neoplasms / genetics. Receptor, Epidermal Growth Factor / genetics

Genetic Alliance. consumer health - Sinus cancer.

NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .

[Email] Email this result item

Email the results to the following email address:   [X] Close

[Cites] Ann Otol Rhinol Laryngol. 2001 Jan;110(1):76-82 [11201814.001]

[Cites] Ann Oncol. 2008 Apr;19(4):717-23 [17974556.001]

[Cites] Mod Pathol. 2002 Mar;15(3):264-78 [11904342.001]

[Cites] Pathol Int. 2003 Jan;53(1):58-65 [12558872.001]

[Cites] J Clin Oncol. 2003 May 15;21(10):1980-7 [12743152.001]

[Cites] J Clin Oncol. 2004 Jan 1;22(1):77-85 [14701768.001]

[Cites] Histopathology. 2004 Jun;44(6):570-9 [15186272.001]

[Cites] Proc Natl Acad Sci U S A. 2004 Sep 7;101(36):13306-11 [15329413.001]

[Cites] Ear Nose Throat J. 2004 Aug;83(8):530, 532 [15487631.001]

[Cites] Otolaryngol Head Neck Surg. 1982 Jul-Aug;90(4):516-7 [6294577.001]

[Cites] Otolaryngol Head Neck Surg. 1986 Jul;95(1):99-103 [3033580.001]

[Cites] ORL J Otorhinolaryngol Relat Spec. 1991;53(4):210-9 [1653928.001]

[Cites] N Engl J Med. 2006 Feb 9;354(6):567-78 [16467544.001]

[Cites] J Laryngol Otol. 2006 Apr;120(4):289-97 [16526967.001]

[Cites] Virchows Arch. 2006 Jul;449(1):135-6 [16570181.001]

[Cites] Acta Otorhinolaryngol Belg. 2001;55(3):251-7 [11685964.001]

(PMID = 20961443.001).

[ISSN] 1477-7819

[Journal-full-title] World journal of surgical oncology

[ISO-abbreviation] World J Surg Oncol

[Language] eng

[Publication-type] Case Reports; Journal Article; Research Support, Non-U.S. Gov't

[Publication-country] England

[Chemical-registry-number] 0 / DNA, Neoplasm; EC 2.7.10.1 / Receptor, Epidermal Growth Factor

[Other-IDs] NLM/ PMC2984401

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] Carcinosarcoma of the oesophagus - a rare mixed type of tumor.

Oesophageal carcinosarcoma is a rare type of oesophageal cancer composed of both squamous cells and sarcomatous cells.

On surgical pathology, it was discovered that the tumor had both squamous cell and sarcomatous cell components, and the final diagnosis was changed to oesophageal carcinosarcoma.

[Email] Email this result item

Email the results to the following email address:   [X] Close

[Copyright] © JSCR.

(PMID = 24946341.001).

[ISSN] 2042-8812

[Journal-full-title] Journal of surgical case reports

[ISO-abbreviation] J Surg Case Rep

[Language] eng

[Publication-type] Journal Article

[Publication-country] England

[Other-IDs] NLM/ PMC3649142

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] Placental site nodule: a tumor-like trophoblastic lesion.

This entity may have bizarre histologic findings and should be distinguished from other aggressive lesions like placental site trophoblastic tumor, epithelioid trophoblastic tumor and squamous cell carcinoma.

[MeSH-major] Gestational Trophoblastic Disease / diagnosis. Placenta Diseases / pathology. Trophoblasts / pathology

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 19332926.001).

[ISSN] 0974-5130

[Journal-full-title] Indian journal of pathology & microbiology

[ISO-abbreviation] Indian J Pathol Microbiol

[Language] eng

[Publication-type] Case Reports; Journal Article

[Publication-country] India

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] Predictors of postoperative stricture after esophageal endoscopic submucosal dissection for superficial squamous cell neoplasms.

BACKGROUND AND STUDY AIMS: Although endoscopic submucosal dissection (ESD) is becoming accepted as an established treatment for superficial esophageal squamous cell neoplasms, the risks for developing postoperative stricture have not been elucidated.

From January 2002 to October 2008, 65 patients with high-grade intraepithelial neoplasms (HGINs) or m2 carcinomas treated by ESD were enrolled.

Predictors of postoperative stricture were investigated by comparing results from 11 patients who developed strictures with those from 54 patients who did not.

[MeSH-major] Esophageal Neoplasms / surgery. Esophageal Stenosis / etiology. Esophagoscopy. Mucous Membrane / surgery. Neoplasms, Squamous Cell / surgery. Postoperative Complications

MedlinePlus Health Information. consumer health - After Surgery.

MedlinePlus Health Information. consumer health - Esophageal Cancer.

ClinicalTrials.gov. clinical trials - ClinicalTrials.gov .

[Email] Email this result item

Email the results to the following email address:   [X] Close

[CommentIn] Endoscopy. 2009 Aug;41(8):712-4 [19670140.001]

(PMID = 19565442.001).

[ISSN] 1438-8812

[Journal-full-title] Endoscopy

[ISO-abbreviation] Endoscopy

[Language] eng

[Publication-type] Journal Article

[Publication-country] Germany

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] Distribution of Bcl-2 gene expression and its prognostic value in non-small cell lung cancer.

The aim of this study was to determine the expression of Bcl-2 gene and prognostic importance of Bcl-2 expression in paraffin embedded blocks of patients diagnosed with non-small cell lung cancer (NSCLC).

These sections are transferred on to slides covered with poly-L-lysine, then de-paraffinization was made.

Positive staining was observed in 9 (19.6%) patients, but not in 37 (80.4%) patients.

Out of 32 cases with squamous cell tumor, 8 (25%) were observed to have positive staining in their sections, but 24 (75%) were not so.

No staining was observed in 11 cases whose cell type was adenoma and two cases whose cell type was adenosquamos (100%).

Staining was present in the section of one case with large cell (100%).

Median survival time was 36.6 months in cases in which staining was observed and 6.10 months in cases in which staining was not observed, with a significant difference (p< 0.05).

[MeSH-major] Carcinoma, Non-Small-Cell Lung / genetics. Gene Expression Regulation, Neoplastic. Genes, bcl-2. Lung Neoplasms / genetics. Proto-Oncogene Proteins c-bcl-2 / biosynthesis

[MeSH-minor] Adenocarcinoma / genetics. Adenocarcinoma / metabolism. Adenocarcinoma / mortality. Adenocarcinoma / pathology. Adult. Aged. Biomarkers, Tumor / metabolism. Female. Humans. Immunohistochemistry. Male. Middle Aged. Prognosis. Retrospective Studies. Survival Rate

Genetic Alliance. consumer health - Lung Cancer.

Genetic Alliance. consumer health - Non-small cell lung cancer.

MedlinePlus Health Information. consumer health - Lung Cancer.

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 16456730.001).

[ISSN] 0494-1373

[Journal-full-title] Tüberküloz ve toraks

[ISO-abbreviation] Tuberk Toraks

[Language] eng

[Publication-type] Journal Article

[Publication-country] Turkey

[Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / Proto-Oncogene Proteins c-bcl-2

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

The cytotoxic activities of these compounds were evaluated against human chronic myeloid leukemia cells (K562) and a human nasopharyngeal epidermoid tumor cell line (KB).

Hazardous Substances Data Bank. GENISTEIN .

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 17311236.001).

[ISSN] 1612-1880

[Journal-full-title] Chemistry & biodiversity

[ISO-abbreviation] Chem. Biodivers.

[Language] eng

[Publication-type] Journal Article; Research Support, Non-U.S. Gov't

[Publication-country] Switzerland

[Chemical-registry-number] 0 / Antineoplastic Agents; DH2M523P0H / Genistein

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] Tumor volume as outcome determinant in patients treated with chemoradiation for locally advanced esophageal cancer.

OBJECTIVE: The currently used tumor-node metastasis (TNM) staging method is generally not applicable to patients with unresectable esophageal carcinomas.

There is a need for both an efficient, easy-to-perform clinical classification and for identification of pretherapeutic prognostic factors that would be useful for oncologists, one of which is tumor volume.

Using the computed tomography (CT) scan classification, tumors were recorded as follows: 1 T1, 42 T2, 93 T3, 6 T4, 2 Nx, 72 N0, 74 N1.

Tumor volume from the CT scans was determined as the sum of 2 opposed truncated cones.

Median tumor volume was 57.5 cm3 (range, 0.6-288 cm3).

Prognostic factors identified by univariate analysis were: dysphagia grade > or =2, other histology than squamous cell, tumor location below the carina, age <65 years and tumor volume > or =100 cm3.

Prognostic factors identified with multivariate analysis were: dysphagia grade > or =2 (P = 0.013), weight loss > or =10% (P = 0.047), tumor location below the carina (P = 0.002), and tumor volume > or =100 cm3 (P = 0.041).

CONCLUSIONS: For patients that the TNM staging system is not applicable, tumor volume is a new powerful determinant of survival.

[MeSH-major] Esophageal Neoplasms / pathology. Neoplasm Staging / methods

Genetic Alliance. consumer health - Esophageal Cancer.

MedlinePlus Health Information. consumer health - Esophageal Cancer.

ClinicalTrials.gov. clinical trials - ClinicalTrials.gov .

[Email] Email this result item

Email the results to the following email address:   [X] Close

[ErratumIn] Am J Clin Oncol. 2007 Feb;30(1):7. Fabrice, Lorchel [corrected to Lorchel, Fabrice]

(PMID = 17148995.001).

[ISSN] 1537-453X

[Journal-full-title] American journal of clinical oncology

[ISO-abbreviation] Am. J. Clin. Oncol.

[Language] eng

[Publication-type] Evaluation Studies; Journal Article

[Publication-country] United States

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

There were 54 parenchymal (lung) tumors and the remaining three tumor cases were mediastinal.

The most common tumor was squamous cell carcinoma (42.6%) followed by adenocarcinoma (29.6%) and small cell carcinoma.

[Email] Email this result item

Email the results to the following email address:   [X] Close

[Cites] Radiology. 1999 Jul;212(1):165-8 [10405737.001]

[Cites] Acta Cytol. 2000 May-Jun;44(3):344-8 [10833989.001]

[Cites] Radiology. 2001 Feb;218(2):491-6 [11161167.001]

[Cites] Radiology. 2002 Dec;225(3):823-8 [12461267.001]

[Cites] Indian J Pathol Microbiol. 2007 Jan;50(1):51-5 [17474259.001]

[Cites] Clin Chest Med. 1993 Mar;14(1):99-110 [8462251.001]

[Cites] J Clin Pathol. 1996 Oct;49(10):839-43 [8943753.001]

[Cites] Singapore Med J. 2002 Nov;43(11):570-5 [12680526.001]

[Cites] Ulster Med J. 2004 May;73(1):32-6 [15244123.001]

[Cites] Clin Chest Med. 1992 Mar;13(1):1-9 [1582141.001]

[Cites] Radiology. 1988 May;167(2):457-61 [3357956.001]

[Cites] Indian J Pathol Microbiol. 2007 Jan;50(1):56-8 [17474260.001]

(PMID = 21938153.001).

[ISSN] 0970-9371

[Journal-full-title] Journal of cytology

[ISO-abbreviation] J Cytol

[Language] ENG

[Publication-type] Journal Article

[Publication-country] India

[Other-IDs] NLM/ PMC3168019

[Keywords] NOTNLM ; CT guided FNAC / lung / thoracic mass lesions

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

Specific subsets include women with peritoneal carcinomatosis, women with isolated axillary lymph node metastases, adenocarcinoma presenting as a single metastatic lesion, young men with features of extragonadal germ cell tumor, squamous carcinoma involving cervical or inguinal lymph nodes, and neuroendocrine carcinoma.

[MeSH-major] Neoplasms, Unknown Primary / therapy

[MeSH-minor] Biomarkers, Tumor / analysis. Humans. Prognosis

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 19179187.001).

[ISSN] 0093-7754

[Journal-full-title] Seminars in oncology

[ISO-abbreviation] Semin. Oncol.

[Language] eng

[Publication-type] Journal Article; Research Support, Non-U.S. Gov't; Review

[Publication-country] United States

[Chemical-registry-number] 0 / Biomarkers, Tumor

[Number-of-references] 58

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

Eleven C2-substituted derivatives of resveratrol (trans-3,4',5-trihydroxystilbene, RES) were prepared by partial synthesis from RES and evaluated for their cytotoxic activities against a human nasopharyngeal epidermoid tumor cell line KB.

Hazardous Substances Data Bank. RESVERATROL .

NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 17000031.001).

[ISSN] 0223-5234

[Journal-full-title] European journal of medicinal chemistry

[ISO-abbreviation] Eur J Med Chem

[Language] eng

[Publication-type] Journal Article; Research Support, Non-U.S. Gov't

[Publication-country] France

[Chemical-registry-number] 0 / Antineoplastic Agents; 0 / Stilbenes; Q369O8926L / resveratrol

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

Survivin overexpression has been reported in relation to tumor malignancy, suggesting that it is an unfavorable prognostic marker, and antibody responses to this protein have been confirmed in human cancer patients.

The cut-off value for positivity in the anti-survivin ELISA was 0.35, as determined using the mean absorbance +2 S.D. of samples from healthy dogs.

Sera from 16 of 59 (27.1%) cancer and 3 of 25 (12%) non-cancer disease dogs were positive on ELISA.

The highest positivity rates (>50%) among the cancer cases were seen in dogs with mammary tumor, squamous cell carcinoma and melanoma.

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 20179386.001).

[ISSN] 0916-7250

[Journal-full-title] The Journal of veterinary medical science

[ISO-abbreviation] J. Vet. Med. Sci.

[Language] ENG

[Publication-type] Journal Article

[Publication-country] Japan

[Chemical-registry-number] 0 / Autoantibodies; 0 / DNA Primers; 0 / Microtubule-Associated Proteins

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] Premalignant neoplasms and squamous cell carcinoma of the anal margin.

Understanding anal anatomy and performing a biopsy of any suspicious lesions are essential in avoiding a delay in diagnosis and appropriately treating these tumors.

Combined multimodality treatment has come to play an important role in managing patient with more advanced or metastatic disease.

[Email] Email this result item

Email the results to the following email address:   [X] Close

[Cites] Dis Colon Rectum. 1997 Aug;40(8):912-8 [9269807.001]

[Cites] J Am Coll Surg. 1997 Nov;185(5):494-505 [9358099.001]

[Cites] Dis Colon Rectum. 2005 Sep;48(9):1742-51 [15991058.001]

[Cites] Dis Colon Rectum. 2005 May;48(5):1042-54 [15868241.001]

[Cites] Dis Colon Rectum. 2005 Mar;48(3):444-50 [15747068.001]

[Cites] Dis Colon Rectum. 2004 Oct;47(10):1655-60; discussion 1660-1 [15540295.001]

[Cites] Arch Dermatol. 1999 Jul;135(7):790-3 [10411153.001]

[Cites] Dis Colon Rectum. 1999 Jul;42(7):945-51 [10411443.001]

[Cites] Dis Colon Rectum. 1997 Nov;40(11):1286-93 [9369101.001]

[Cites] N Engl J Med. 1997 Nov 6;337(19):1350-8 [9358129.001]

[Cites] Ann Surg Oncol. 1997 Sep;4(6):475-80 [9309336.001]

[Cites] Surg Oncol. 1996 Feb;5(1):29-35 [8837302.001]

[Cites] J Am Acad Dermatol. 1992 Dec;27(6 Pt 1):979-82 [1479105.001]

[Cites] Dis Colon Rectum. 1992 May;35(5):422-9 [1568392.001]

[Cites] Lasers Surg Med. 1991;11(4):385-7 [1895869.001]

[Cites] JAMA. 1991 Aug 14;266(6):816-9 [1865520.001]

[Cites] Br J Dermatol. 1988 Aug;119(2):231-40 [3166941.001]

[Cites] Surg Oncol Clin N Am. 2004 Apr;13(2):321-38 [15137960.001]

[Cites] J Surg Oncol. 2004 May 1;86(2):55-62; discussion 63 [15112245.001]

[Cites] Cancer Invest. 2003 Jun;21(3):452-64 [12901291.001]

[Cites] Dis Colon Rectum. 2003 May;46(5):612-6 [12792436.001]

[Cites] Surg Clin North Am. 2002 Dec;82(6):1233-51 [12516851.001]

[Cites] Br J Cancer. 2002 Jul 1;87(1):61-4 [12085257.001]

[Cites] Am J Surg. 2001 Apr;181(4):363-5 [11438274.001]

[Cites] Dis Colon Rectum. 2001 Jun;44(6):868-70 [11391150.001]

[Cites] Hematol Oncol Clin North Am. 2001 Apr;15(2):321-44, vi [11370496.001]

[Cites] J Natl Cancer Inst. 2000 Sep 20;92(18):1500-10 [10995805.001]

[Cites] Dis Colon Rectum. 2000 Apr;43(4):499-502 [10789745.001]

[Cites] Br J Surg. 1988 Nov;75(11):1089-92 [2850073.001]

[Cites] Dis Colon Rectum. 1987 Apr;30(4):263-6 [3030676.001]

[Cites] Dis Colon Rectum. 1988 Jun;31(6):419-22 [3288448.001]

[Cites] Dis Colon Rectum. 1988 Apr;31(4):273-8 [3359896.001]

[Cites] JAMA. 1987 Jan 23-30;257(4):516-8 [3795434.001]

[Cites] Dis Colon Rectum. 1983 Nov;26(11):712-5 [6628143.001]

[Cites] Dis Colon Rectum. 1974 May-Jun;17(3):354-6 [4830803.001]

[Cites] Surg Oncol Clin N Am. 2004 Apr;13(2):375-88 [15137963.001]

(PMID = 20011315.001).

[ISSN] 1530-9681

[Journal-full-title] Clinics in colon and rectal surgery

[ISO-abbreviation] Clin Colon Rectal Surg

[Language] eng

[Publication-type] Journal Article

[Publication-country] United States

[Other-IDs] NLM/ PMC2780101

[Keywords] NOTNLM ; Anus neoplasms / Bowen's disease / Paget's disease / squamous cell cancer

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

The most common malignant tumor was squamous cell carcinoma (41, 1%) and then cancers of salivary origin (20, 2%).

Within the maxillary sinus the most frequent neoplasm was cancer whereas in the nasal cavity melanoma and olfactory neuroblastoma.

In three (2, 4%) patients site of tumor origin demonstrated on CT was different form that of operative finding.

[MeSH-major] Maxillary Sinus Neoplasms / pathology. Nose Neoplasms / pathology. Paranasal Sinus Neoplasms / secondary. Salivary Gland Neoplasms / pathology

[MeSH-minor] Adolescent. Adult. Aged. Aged, 80 and over. Carcinoma, Squamous Cell / secondary. Child. Child, Preschool. Esthesioneuroblastoma, Olfactory / secondary. Female. Humans. Male. Melanoma / secondary. Middle Aged. Tomography, X-Ray Computed

MedlinePlus Health Information. consumer health - Nasal Cancer.

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 16358890.001).

[ISSN] 1426-9686

[Journal-full-title] Polski merkuriusz lekarski : organ Polskiego Towarzystwa Lekarskiego

[ISO-abbreviation] Pol. Merkur. Lekarski

[Language] pol

[Publication-type] English Abstract; Journal Article

[Publication-country] Poland

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] Nail unit tumors: a study of 234 patients in the dermatology department of the "Dr Manuel Gea González" General Hospital in Mexico City.

BACKGROUND: The frequency of nail unit tumors is not well known because they are often misdiagnosed, and the clinical appearance of benign and malignant tumors is not characteristic.

RESULTS: The tumors most frequently diagnosed were fibrous tumors (29.05%), osteocartilaginous tumors (21.79%), and myxoid pseudocysts (11.96%).

Malignant melanoma occupied the fourth place (9.82%), and the second most frequent malignant tumor was squamous cell carcinoma (SCC; 4.70%).

Among other tumors were glomus, neurofibromas, giant cell tumors of tendon sheath, and pyogenic granulomas.

CONCLUSION: This study in a Mexican population sheds light on the frequency and the alterations produced by nail unit tumors, which we must keep in mind for a more accurate diagnosis.

[MeSH-major] Nail Diseases / diagnosis. Skin Neoplasms / diagnosis

MedlinePlus Health Information. consumer health - Nail Diseases.

MedlinePlus Health Information. consumer health - Skin Cancer.

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 18616533.001).

[ISSN] 1524-4725

[Journal-full-title] Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.]

[ISO-abbreviation] Dermatol Surg

[Language] eng

[Publication-type] Journal Article

[Publication-country] United States

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

The cytotoxic activities of these compounds were evaluated against a human nasopharyngeal epidermoid tumor cell line KB.

[MeSH-minor] Cell Line, Tumor. Drug Screening Assays, Antitumor / methods. Humans

Hazardous Substances Data Bank. GENISTEIN .

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 17193282.001).

[ISSN] 1612-1880

[Journal-full-title] Chemistry & biodiversity

[ISO-abbreviation] Chem. Biodivers.

[Language] eng

[Publication-type] Comparative Study; Journal Article; Research Support, Non-U.S. Gov't

[Publication-country] Switzerland

[Chemical-registry-number] 0 / Cytotoxins; DH2M523P0H / Genistein

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

Keratoacanthomas are squamous cell neoplasms known to be abundant in epidermal growth factor receptors (EGFRs).

[MeSH-major] Head and Neck Neoplasms / drug therapy. Keratoacanthoma / drug therapy. Protein Kinase Inhibitors / therapeutic use. Quinazolines / therapeutic use. Scalp. Skin Neoplasms / drug therapy

Genetic Alliance. consumer health - Keratoacanthoma.

MedlinePlus Health Information. consumer health - Head and Neck Cancer.

MedlinePlus Health Information. consumer health - Skin Cancer.

COS Scholar Universe. author profiles.

NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .

[Email] Email this result item

Email the results to the following email address:   [X] Close

[Copyright] © 2010 The Authors. Journal Compilation © 2010 British Association of Dermatologists.

(PMID = 20222923.001).

[ISSN] 1365-2133

[Journal-full-title] The British journal of dermatology

[ISO-abbreviation] Br. J. Dermatol.

[Language] eng

[Publication-type] Case Reports; Journal Article

[Publication-country] England

[Chemical-registry-number] 0 / Protein Kinase Inhibitors; 0 / Quinazolines; DA87705X9K / Erlotinib Hydrochloride; EC 2.7.10.1 / Receptor, Epidermal Growth Factor

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

Patients with inoperable cancer of the esophagus were followed up for 1-3 years after a course of palliative endoscopic destruction of tumor.

Among the unfavorable prognostic factors were partial decomposition of tumor, squamous-cell pattern, size of more than 9 cm, circular extension through the esophagus and stage III stenosis.

[MeSH-major] Esophageal Neoplasms / surgery. Esophagoscopy. Palliative Care / methods

[MeSH-minor] Adult. Aged. Aged, 80 and over. Carcinoma, Squamous Cell / surgery. Follow-Up Studies. Humans. Middle Aged. Risk Factors. Severity of Illness Index. Survival Analysis. Treatment Outcome

MedlinePlus Health Information. consumer health - Esophageal Cancer.

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 16756018.001).

[ISSN] 0507-3758

[Journal-full-title] Voprosy onkologii

[ISO-abbreviation] Vopr Onkol

[Language] rus

[Publication-type] English Abstract; Journal Article

[Publication-country] Russia (Federation)

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] Preoperative transvaginal ultrasound guided needle biopsy for primary squamous cell carcinoma of the endometrium.

Primary squamous cell carcinoma of the endometrium (PSCCE) is an extremely rare tumor and little information is available about its treatment and prognosis.

Magnetic resonance imaging (MRI) demonstrated a uterine tumor and transvaginal ultrasound guided needle biopsy specimens of the tumor showed squamous cell carcinoma.

She remains free of disease at 6 months after CCRT.

[MeSH-major] Biopsy, Needle / methods. Carcinoma, Squamous Cell / pathology. Endometrial Neoplasms / pathology. Ultrasonography / methods

Genetic Alliance. consumer health - Carcinoma, Squamous Cell.

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 21058445.001).

[ISSN] 1447-0756

[Journal-full-title] The journal of obstetrics and gynaecology research

[ISO-abbreviation] J. Obstet. Gynaecol. Res.

[Language] eng

[Publication-type] Case Reports; Journal Article

[Publication-country] Australia

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] Monoclonal antibody Ber-EP4 reliably discriminates between microcystic adnexal carcinoma and basal cell carcinoma.

BACKGROUND: Sclerosing cutaneous neoplasms often represent a diagnostic challenge.

It is diagnostically highly reliable in the differentiation between basal cell carcinoma and cutaneous squamous cell carcinoma.

In this study, we report its application in the differential diagnosis of microcystic adnexal carcinoma, desmoplastic trichoepithelioma and basal cell carcinoma.

METHODS: Biopsy samples from 28 sclerosing and infiltrating basal cell carcinomas, 13 microcystic adnexal carcinomas and 16 desmoplastic trichoepitheliomas were examined after immunohistochemical staining with Ber-EP4.

RESULTS: Ber-EP4 did not label any of the microcystic adnexal carcinomas, whereas all 28 basal cell carcinomas were Ber-EP4 positive.

Only one basal cell carcinoma was weakly positive.

Twelve of the 16 desmoplastic trichoepitheliomas were immunoreactive with Ber-EP4 and the staining was more variable than those of basal cell carcinomas.

CONCLUSIONS: Ber-EP4 reliably differentiates microcystic adnexal carcinoma from basal cell carcinoma to the same extent as it distinguishes the latter tumor from squamous cell carcinoma.

While it stains the majority of desmoplastic trichoepitheliomas, these tumors still have to be considered in the differential diagnosis with microcystic adnexal carcinoma, when Ber-EP4 is applied.

[MeSH-major] Biomarkers, Tumor / metabolism. Carcinoma, Basal Cell / diagnosis. Carcinoma, Skin Appendage / diagnosis. Skin / pathology. Skin Neoplasms / diagnosis

[MeSH-minor] Biopsy. Carcinoma, Squamous Cell / diagnosis. Carcinoma, Squamous Cell / metabolism. Diagnosis, Differential. Fluorescent Antibody Technique, Indirect. Humans. Sclerosis / pathology

Genetic Alliance. consumer health - Microcystic adnexal carcinoma.

MedlinePlus Health Information. consumer health - Skin Cancer.

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 17880584.001).

[ISSN] 0303-6987

[Journal-full-title] Journal of cutaneous pathology

[ISO-abbreviation] J. Cutan. Pathol.

[Language] eng

[Publication-type] Journal Article

[Publication-country] Denmark

[Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / human epithelial antigen-125

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] Activator protein-1 activity regulates epithelial tumor cell identity.

When A-FOS was expressed during chemical-induced skin carcinogenesis, mice do not develop characteristic benign and malignant squamous lesions but instead develop benign sebaceous adenomas containing a signature mutation in the H-ras proto-oncogene.

Inhibiting AP-1 activity after tumor formation caused squamous tumors to transdifferentiate into sebaceous tumors.

Furthermore, reactivating AP-1 in sebaceous tumors results in a reciprocal transdifferentiation into squamous tumors.

In both cases of transdifferentiation, individual cells express molecular markers for both cell types, indicating individual tumor cells have the capacity to express multiple lineages.

Molecular characterization of cultured keratinocytes and tumor material indicates that AP-1 regulates the balance between the wnt/beta-catenin and hedgehog signaling pathways that determine squamous and sebaceous lineages, respectively.

Thus, AP-1 activity regulates tumor cell lineage and is essential to maintain the squamous tumor cell identity.

[MeSH-major] Adenocarcinoma, Sebaceous / metabolism. Carcinoma, Squamous Cell / metabolism. Skin Neoplasms / metabolism. Transcription Factor AP-1 / metabolism

[MeSH-minor] Animals. DNA, Neoplasm / metabolism. Hyperplasia. Keratinocytes / metabolism. Mice. Mice, Transgenic. Precancerous Conditions / genetics. Precancerous Conditions / metabolism. Precancerous Conditions / pathology. Promoter Regions, Genetic. Protein Binding. Proto-Oncogene Proteins c-fos / biosynthesis. Proto-Oncogene Proteins c-fos / genetics. Proto-Oncogene Proteins c-jun / metabolism. Sebaceous Glands / pathology. Transcriptional Activation. Wnt Proteins / genetics

MedlinePlus Health Information. consumer health - Skin Cancer.

COS Scholar Universe. author profiles.

KOMP Repository. gene/protein/disease-specific - KOMP Repository (subscription/membership/fee required).

Mouse Genome Informatics (MGI). Mouse Genome Informatics (MGI) .

NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .

NCI CPTC Antibody Characterization Program. NCI CPTC Antibody Characterization Program .

NCI CPTC Antibody Characterization Program. NCI CPTC Antibody Characterization Program .

NCI CPTC Antibody Characterization Program. NCI CPTC Antibody Characterization Program .

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 16885357.001).

[ISSN] 0008-5472

[Journal-full-title] Cancer research

[ISO-abbreviation] Cancer Res.

[Language] eng

[Grant] United States / Intramural NIH HHS / /

[Publication-type] Journal Article; Research Support, N.I.H., Intramural

[Publication-country] United States

[Chemical-registry-number] 0 / DNA, Neoplasm; 0 / Proto-Oncogene Proteins c-fos; 0 / Proto-Oncogene Proteins c-jun; 0 / Transcription Factor AP-1; 0 / Wnt Proteins

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Transliterated title] Cuidados vocais: questão de prevenção e saúde.

Considering all the patients attended, only one presented malignant neoplasm (squamous cell carcinoma), confirmed later by biopsy.

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 20922288.001).

[ISSN] 1678-4561

[Journal-full-title] Ciência & saúde coletiva

[ISO-abbreviation] Cien Saude Colet

[Language] por

[Publication-type] English Abstract; Journal Article

[Publication-country] Brazil

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

The X-ray induction of tumors was examined in five-week-old male Otsuka Long-Evans Tokushima Fatty (OLETF) rats, treated with two 10 Gy doses to the gastric region with a 3-day interval (total 20 Gy).

The total tumor incidence was 27/30 (87.1%) in the treated rats (islet tumors, gastric tumors, sarcomas, seminomas, adrenal tumors, kidney tumors, papilloma, lymphomas and mammary tumors).

Islet tumors, generally showed to be positive for insulin by immunohistochemistry, developed in 19 rats (63.3%), and were associated with low serum glucose.

Since spontaneous tumors observed in 6/19 (31.6%) rats (sarcomas, kidney tumors, duodenum tumors, seminoma, adrenal tumor and squamous cell carcinoma) did not include any insulinomas, these are clearly induced by X-irradiation in OLETF rats.

[MeSH-major] Insulinoma / etiology. Neoplasms, Radiation-Induced / etiology. Pancreatic Neoplasms / etiology

MedlinePlus Health Information. consumer health - Pancreatic Cancer.

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 18357386.001).

[ISSN] 1021-335X

[Journal-full-title] Oncology reports

[ISO-abbreviation] Oncol. Rep.

[Language] eng

[Publication-type] Journal Article

[Publication-country] Greece

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] Metastatic tumors in the breast: a report of 5 cases and review of the literature.

However, metastases to the breast from nonmammary malignant neoplasms are rare and were detected at a rate of 0.28% in our series.

Clinical and pathologic findings in 5 cases of metastatic tumors (malign mesenchymal tumor, squamous cell carcinoma of the tongue, non-Hodgkin lymphoma, and Sézary syndrome) in the breast are presented and discussed with respect to the literature.

[MeSH-major] Breast Neoplasms / secondary. Carcinoma, Squamous Cell / secondary. Histiocytoma, Malignant Fibrous / secondary. Lymphoma, Large B-Cell, Diffuse / pathology. Sezary Syndrome / pathology

[MeSH-minor] Adult. Aged. Female. Humans. Middle Aged. Skin Neoplasms / pathology

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 17592678.001).

[ISSN] 1526-8209

[Journal-full-title] Clinical breast cancer

[ISO-abbreviation] Clin. Breast Cancer

[Language] eng

[Publication-type] Case Reports; Journal Article; Review

[Publication-country] United States

[Number-of-references] 25

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

Gestational trophoblastic disease refers to a spectrum of proliferative disorders of the placental trophoblast, with a wide range of histologic appearances and clinical behaviors.

A discussion of epithelioid trophoblastic tumor, a newly introduced tumor subtype, with its differential diagnosis from placental-site trophoblastic tumor and squamous cell carcinoma is also presented.

[MeSH-major] Gestational Trophoblastic Disease / pathology

[MeSH-minor] Carcinoma, Squamous Cell / pathology. Choriocarcinoma / pathology. Diagnosis, Differential. Female. Humans. Hydatidiform Mole / pathology. Hydatidiform Mole, Invasive / pathology. Pregnancy. Trophoblastic Tumor, Placental Site / pathology. Uterine Neoplasms / pathology

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 15900112.001).

[ISSN] 1072-4109

[Journal-full-title] Advances in anatomic pathology

[ISO-abbreviation] Adv Anat Pathol

[Language] eng

[Publication-type] Journal Article; Review

[Publication-country] United States

[Number-of-references] 66

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] Loss of the Atp2c1 secretory pathway Ca(2+)-ATPase (SPCA1) in mice causes Golgi stress, apoptosis, and midgestational death in homozygous embryos and squamous cell tumors in adult heterozygotes.

Loss of one copy of the human ATP2C1 gene, encoding SPCA1 (secretory pathway Ca(2+)-ATPase isoform 1), causes Hailey-Hailey disease, a skin disorder.

Breeding of heterozygous mutants yielded a normal Mendelian ratio among embryos on gestation day 9.5; however, null mutant (Spca1(-/-)) embryos exhibited growth retardation and did not survive beyond gestation day 10.5.

Coated pits, junctional complexes, desmosomes, and basement membranes appeared normal in mutant embryos, indicating that processing and trafficking of proteins in the secretory pathway was not massively impaired.

Adult heterozygous mice appeared normal and exhibited no evidence of Hailey-Hailey disease; however, aged heterozygotes had an increased incidence of squamous cell tumors of keratinized epithelial cells of the skin and esophagus.

[MeSH-major] Calcium-Transporting ATPases / deficiency. Carcinoma, Squamous Cell / metabolism. Embryo Loss / metabolism. Esophageal Neoplasms / metabolism. Golgi Apparatus / metabolism. Loss of Heterozygosity. Skin Neoplasms / metabolism

[MeSH-minor] Aging / genetics. Aging / metabolism. Aging / pathology. Animals. Apoptosis / genetics. Basement Membrane / metabolism. Basement Membrane / ultrastructure. Cardiovascular System / embryology. Coated Pits, Cell-Membrane / genetics. Coated Pits, Cell-Membrane / metabolism. Coated Pits, Cell-Membrane / ultrastructure. Desmosomes / genetics. Desmosomes / metabolism. Desmosomes / ultrastructure. Endoplasmic Reticulum, Rough / genetics. Endoplasmic Reticulum, Rough / metabolism. Endoplasmic Reticulum, Rough / ultrastructure. Female. Genetic Predisposition to Disease. Hematopoiesis / genetics. Heterozygote. Homozygote. Humans. Inbreeding. Male. Mice. Mice, Knockout. Neural Tube Defects / embryology. Neural Tube Defects / metabolism. Neural Tube Defects / pathology. Pemphigus, Benign Familial / genetics. Pemphigus, Benign Familial / metabolism. Pemphigus, Benign Familial / pathology. Pregnancy. Protein Transport / genetics. Ribosomes / metabolism. Secretory Vesicles / genetics. Secretory Vesicles / metabolism. Secretory Vesicles / ultrastructure. Water-Electrolyte Balance / genetics

MedlinePlus Health Information. consumer health - Esophageal Cancer.

MedlinePlus Health Information. consumer health - Skin Cancer.

COS Scholar Universe. author profiles.

Jackson Laboratory JAX®Mice Database. culture/stock collections - B6.129X1(Cg)-Atp2c1<tm1Ges>/Mmjax (subscription/membership/fee required).

KOMP Repository. gene/protein/disease-specific - KOMP Repository (subscription/membership/fee required).

Mouse Genome Informatics (MGI). Mouse Genome Informatics (MGI) .

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 17597066.001).

[ISSN] 0021-9258

[Journal-full-title] The Journal of biological chemistry

[ISO-abbreviation] J. Biol. Chem.

[Language] eng

[Grant] United States / NIDDK NIH HHS / DK / DK50594; United States / NIEHS NIH HHS / ES / ES06096; United States / NHLBI NIH HHS / HL / HL61974

[Publication-type] Comparative Study; Journal Article; Research Support, N.I.H., Extramural

[Publication-country] United States

[Chemical-registry-number] EC 3.6.3.8 / ATP2C1 protein, human; EC 3.6.3.8 / Atp2c1 protein, mouse; EC 3.6.3.8 / Calcium-Transporting ATPases

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] Comparison of survival and recurrence pattern between two-field and three-field lymph node dissections for upper thoracic esophageal squamous cell carcinoma.

The objective of this study was to compare survival and recurrence according to the extent of lymph node dissection in patients with upper thoracic esophageal squamous cell cancer.

METHODS: Between 1995 and 2007, 91 patients underwent R0 esophagectomy (with no residual tumor) for squamous cell carcinoma of the upper thoracic esophagus at our institution.

The disease-free 5-year survival rate was 39% for the 2 FL group and 38% for the 3 FL group (p = 0.97).

The overall recurrence rate and the incidence of cervical nodal recurrence were not significantly different between the two groups.

CONCLUSIONS: Our findings suggest that there was no survival benefit from the addition of cervical nodal dissection in patients with upper thoracic esophageal squamous cell carcinoma who had no evidence of cervical lymph node metastasis.

[MeSH-major] Carcinoma, Squamous Cell / mortality. Esophageal Neoplasms / mortality. Lymph Node Excision / mortality. Neoplasm Recurrence, Local / mortality. Postoperative Complications / mortality

[MeSH-minor] Esophagectomy. Female. Follow-Up Studies. Humans. Liver Neoplasms / mortality. Liver Neoplasms / secondary. Liver Neoplasms / surgery. Male. Middle Aged. Neoplasm Staging. Survival Rate. Treatment Outcome

Genetic Alliance. consumer health - Carcinoma, Squamous Cell.

MedlinePlus Health Information. consumer health - After Surgery.

MedlinePlus Health Information. consumer health - Esophageal Cancer.

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 20421764.001).

[ISSN] 1556-1380

[Journal-full-title] Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer

[ISO-abbreviation] J Thorac Oncol

[Language] eng

[Publication-type] Comparative Study; Journal Article

[Publication-country] United States

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

The synthesized compounds have been evaluated for their cytotoxic activity against a human nasopharyngeal epidermoid tumor cell line KB, as well as for their xanthine oxidase inhibitory activity.

Compounds 2, 3, and 6a showed the most significant cytotoxic activities against the cell line KB, and compound 2 also exhibited strong xanthine oxidase inhibitory activity.

[MeSH-minor] Antineoplastic Agents / pharmacology. Cell Survival / drug effects. Enzyme Inhibitors / chemical synthesis. Enzyme Inhibitors / pharmacology. Humans. KB Cells / drug effects

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 18421756.001).

[ISSN] 1612-1880

[Journal-full-title] Chemistry & biodiversity

[ISO-abbreviation] Chem. Biodivers.

[Language] eng

[Publication-type] Journal Article; Research Support, Non-U.S. Gov't

[Publication-country] Switzerland

[Chemical-registry-number] 0 / Antineoplastic Agents; 0 / Enzyme Inhibitors; 0 / Phenols; 0 / Stilbenes; EC 1.17.3.2 / Xanthine Oxidase; Q369O8926L / resveratrol

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] Chronic phototoxicity and aggressive squamous cell carcinoma of the skin in children and adults during treatment with voriconazole.

A possible link with aggressive squamous cell carcinoma (SCC) has also been reported.

METHODS: We conducted a retrospective review of patients who developed one or more squamous cell neoplasms during long-term treatment with voriconazole at 3 academic dermatology centers.

Underlying diagnoses included graft-versus-host disease, HIV, and Wegener granulomatosis.

[MeSH-major] Antifungal Agents / adverse effects. Carcinoma, Squamous Cell / chemically induced. Dermatitis, Phototoxic / etiology. Pyrimidines / adverse effects. Skin Neoplasms / chemically induced. Triazoles / adverse effects

[MeSH-minor] Adolescent. Adult. Child. Comorbidity. DNA Damage / radiation effects. Fatal Outcome. Female. Hematopoietic Stem Cell Transplantation. Humans. Immunocompromised Host. Middle Aged. Retrospective Studies. Voriconazole. Young Adult

Genetic Alliance. consumer health - Carcinoma, Squamous Cell.

MedlinePlus Health Information. consumer health - Skin Cancer.

COS Scholar Universe. author profiles.

Faculty of 1000. commentaries/discussion - See the articles recommended by F1000Prime's Faculty of more than 8,000 leading experts in Biology and Medicine. (subscription/membership/fee required).

[Email] Email this result item

Email the results to the following email address:   [X] Close

[Cites] Lancet. 2001 Sep 29;358(9287):1042-5 [11589933.001]

[Cites] Clin Infect Dis. 2009 May 15;48(10):1441-58 [19361301.001]

[Cites] N Engl J Med. 2002 Aug 8;347(6):408-15 [12167683.001]

[Cites] N Engl J Med. 2003 Apr 24;348(17):1681-91 [12711744.001]

[Cites] Int J Dermatol. 2004 Oct;43(10):768-71 [15485539.001]

[Cites] J Photochem Photobiol B. 1997 Feb;37(3):174-81 [9085564.001]

[Cites] Pediatr Dermatol. 2004 Nov-Dec;21(6):675-8 [15575856.001]

[Cites] J Am Acad Dermatol. 2005 May;52(5 Suppl 1):S81-5 [15858516.001]

[Cites] Blood. 2005 May 15;105(10):3802-11 [15687239.001]

[Cites] J Clin Oncol. 2006 Mar 1;24(7):1119-26 [16461782.001]

[Cites] Photodermatol Photoimmunol Photomed. 2007 Feb;23(1):29-31 [17254033.001]

[Cites] Clin Infect Dis. 2007 Mar 1;44(5):e55-6 [17278050.001]

[Cites] Biochem Pharmacol. 2007 Jun 15;73(12):2020-6 [17433262.001]

[Cites] N Engl J Med. 2007 Aug 16;357(7):682-90 [17699818.001]

[Cites] J Drugs Dermatol. 2007 Oct;6(10):1042-4 [17966183.001]

[Cites] J Invest Dermatol. 2007 Dec;127(12):2901-3 [17597817.001]

[Cites] Am J Transplant. 2008 Apr;8(4):877-80 [18261173.001]

[Cites] Photochem Photobiol. 2008 Mar-Apr;84(2):272-83 [18353168.001]

[Cites] AIDS. 2008 Apr 23;22(7):905-6 [18427212.001]

[Cites] Br J Cancer. 2008 Nov 4;99(9):1522-8 [18813314.001]

[Cites] Biol Blood Marrow Transplant. 2009 Mar;15(3):370-6 [19203729.001]

[Cites] Clin Exp Dermatol. 2001 Nov;26(8):648-53 [11722447.001]

(PMID = 19896749.001).

[ISSN] 1097-6787

[Journal-full-title] Journal of the American Academy of Dermatology

[ISO-abbreviation] J. Am. Acad. Dermatol.

[Language] eng

[Grant] United States / Intramural NIH HHS / / Z99 CA999999

[Publication-type] Case Reports; Journal Article; Multicenter Study; Research Support, N.I.H., Intramural

[Publication-country] United States

[Chemical-registry-number] 0 / Antifungal Agents; 0 / Pyrimidines; 0 / Triazoles; JFU09I87TR / Voriconazole

[Other-IDs] NLM/ NIHMS151323; NLM/ PMC2815347

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

(1)H-NMR guided fractionation of the EtOAc extract from the culture of Myrothecium gramminum (strain no. 3.1968) led to the isolation of eight cytotoxic trichothecene macrolides ( 1 - 8), all being substantially inhibitory against HepG2 (human hepatocellular carcinoma) and KB (human nasopharynyeal epidermoid tumor) cell lines with IC (50) values ranging from 2.2 to 12.2 mug/mL.

Their inactivity to or weaker action on Vero cells (IC (50) values > 20 microg/mL, originated from the African green monkey kidney) highlighted preliminarily the nature of the selective cytotoxicity of the fungal metabolites against the test cancer cell lines.

[MeSH-major] Cytotoxins / pharmacology. Hypocreales / chemistry. Macrolides / pharmacology. Neoplasms / drug therapy. Phytotherapy. Poaceae / drug effects

[MeSH-minor] Animals. Cell Line, Tumor. Cercopithecus aethiops. Humans. Liver Neoplasms / drug therapy. Molecular Structure. Nasopharyngeal Neoplasms / drug therapy. Vero Cells

MedlinePlus Health Information. consumer health - Cancer Chemotherapy.

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 19097001.001).

[ISSN] 0032-0943

[Journal-full-title] Planta medica

[ISO-abbreviation] Planta Med.

[Language] eng

[Publication-type] Journal Article; Research Support, Non-U.S. Gov't

[Publication-country] Germany

[Chemical-registry-number] 0 / Cytotoxins; 0 / Macrolides

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

Recipients of pancreas kidney transplants or with suspected but not biopsy-proven skin malignancy were excluded from this series.

The most frequent skin cancer was squamous cell carcinoma (46.2%), in single or multiple lesions (50% each group).

Basal cell carcinoma was diagnosed in seven patients; most presented as a single lesion (71.3%).

Eight patients presented with more than one histologic type of skin cancer; most frequently squamous and basal cell carcinomas.

Kaposi sarcoma was diagnosed in four patients, one of whom also had a basal cell carcinoma.

The most frequent tumor was squamous cell carcinoma, isolated or in association with basal cell carcinoma.

[MeSH-major] Kidney Transplantation / adverse effects. Postoperative Complications / epidemiology. Skin Neoplasms / epidemiology

MedlinePlus Health Information. consumer health - After Surgery.

MedlinePlus Health Information. consumer health - Kidney Transplantation.

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 18455011.001).

[ISSN] 0041-1345

[Journal-full-title] Transplantation proceedings

[ISO-abbreviation] Transplant. Proc.

[Language] eng

[Publication-type] Journal Article

[Publication-country] United States

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] Thorax perfusion CT in non-small cell lung cancer.

OBJECTIVES: We aimed to determine the perfusion differences according to the histological type, stage, volume and prognoses in the non-small cell carcinoma by thorax perfusion CT.

MATERIALS AND METHODS: Twenty-four non-small cell carcinoma patients were included in the study.

Thorax perfusion CT was done to evaluate the tumors in terms of perfusion parameters: blood flow (BF) and time to peak (TTP) values.

RESULTS: The total blood flow of the tumor in squamous cell carcinoma was significantly higher than adenocarcinoma (p=0.031).

CONCLUSIONS: Perfusion CT may help us in evaluating non-small cell carcinomas.

[MeSH-major] Carcinoma, Non-Small-Cell Lung / radiography. Lung Neoplasms / radiography

Genetic Alliance. consumer health - Lung Cancer.

Genetic Alliance. consumer health - Non-small cell lung cancer.

MedlinePlus Health Information. consumer health - Lung Cancer.

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 17904334.001).

[ISSN] 0895-6111

[Journal-full-title] Computerized medical imaging and graphics : the official journal of the Computerized Medical Imaging Society

[ISO-abbreviation] Comput Med Imaging Graph

[Language] eng

[Publication-type] Journal Article

[Publication-country] United States

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

DESIGN: Participant responses between 2000 and 2007 were evaluated for esophageal wash/brush, gastric wash/brush, and biliary tract brush specimens with a reference diagnosis of adenocarcinoma, squamous cell carcinoma, carcinoid, or spindle cell neoplasm.

Overall performance of cytotechnologists was not different from that of pathologists (89.2% versus 89.0%; P = .75).

Cytotechnologists had better performance for detecting squamous cell carcinoma (96.3% versus 92.6%; P < .001), while pathologists had better performance for detecting spindle cell neoplasm (79.7% versus 42.9%; P < .001).

Cytotechnologists and pathologists performed at the same level overall, but with differences for the diagnosis of spindle cell neoplasm and squamous carcinoma.

[MeSH-major] Adenocarcinoma / diagnosis. Carcinoma, Squamous Cell / diagnosis. Gastrointestinal Neoplasms / diagnosis. Laboratories, Hospital / standards. Pathology, Clinical / methods

COS Scholar Universe. author profiles.

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 20670130.001).

[ISSN] 1543-2165

[Journal-full-title] Archives of pathology & laboratory medicine

[ISO-abbreviation] Arch. Pathol. Lab. Med.

[Language] eng

[Publication-type] Comparative Study; Journal Article

[Publication-country] United States

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] Haploinsufficiency of Atp2a2, encoding the sarco(endo)plasmic reticulum Ca2+-ATPase isoform 2 Ca2+ pump, predisposes mice to squamous cell tumors via a novel mode of cancer susceptibility.

A null mutation in one copy of the Atp2a2 or ATP2A2 gene, encoding sarco(endo)plasmic reticulum Ca2+-ATPase isoform 2 (SERCA2), leads to squamous cell tumors in mice and to Darier disease in humans, a skin disorder that also involves keratinocytes.

Here, we examined the time course and genetic mechanisms of tumor development in the mutant animals.

By the age of 5 to 7 months, 22% of mutants had developed papillomas of the forestomach, and 89% of mutants older than 14 months had developed squamous cell papillomas and/or carcinomas, with a preponderance of the latter.

Tumors occurred in regions that had keratinized epithelium and were subjected to repeated mechanical irritation.

The genetic mechanism of tumorigenesis did not involve loss of heterozygosity, as tumor cells analyzed by laser capture microdissection contained the wild-type Atp2a2 allele.

Furthermore, immunoblot and immunohistochemical analysis showed that tumor keratinocytes expressed the SERCA2 protein.

Mutations were not observed in the ras proto-oncogenes; however, expression of wild-type ras was up-regulated, with particularly high levels of K-ras.

Loss of the p53 tumor suppressor gene occurred in a single massive tumor, whereas other tumors had increased levels of p53 protein but no mutations in the p53 gene.

These findings show that SERCA2 haploinsufficiency predisposes mice to tumor development via a novel mode of cancer susceptibility involving a global change in the tumorigenic potential of keratinized epithelium in Atp2a2+/- mice.

[MeSH-major] Calcium-Transporting ATPases / genetics. Carcinoma, Squamous Cell / enzymology. Carcinoma, Squamous Cell / genetics. Stomach Neoplasms / enzymology. Stomach Neoplasms / genetics

[MeSH-minor] Alleles. Animals. Genes, p53. Genes, ras. Genetic Predisposition to Disease. Humans. Keratinocytes / metabolism. Keratins / metabolism. Loss of Heterozygosity. Male. Mice. Sarcoplasmic Reticulum Calcium-Transporting ATPases. Tumor Suppressor Protein p53 / biosynthesis. Tumor Suppressor Protein p53 / genetics

MedlinePlus Health Information. consumer health - Stomach Cancer.

COS Scholar Universe. author profiles.

KOMP Repository. gene/protein/disease-specific - KOMP Repository (subscription/membership/fee required).

Mouse Genome Informatics (MGI). Mouse Genome Informatics (MGI) .

NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 16204033.001).

[ISSN] 0008-5472

[Journal-full-title] Cancer research

[ISO-abbreviation] Cancer Res.

[Language] eng

[Grant] United States / NIDDK NIH HHS / DK / DK50594; United States / NIEHS NIH HHS / ES / ES06096; United States / NHLBI NIH HHS / HL / HL61974

[Publication-type] Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, P.H.S.

[Publication-country] United States

[Chemical-registry-number] 0 / Tumor Suppressor Protein p53; 68238-35-7 / Keratins; EC 3.6.3.8 / ATP2A2 protein, human; EC 3.6.3.8 / Atp2a2 protein, mouse; EC 3.6.3.8 / Calcium-Transporting ATPases; EC 3.6.3.8 / Sarcoplasmic Reticulum Calcium-Transporting ATPases

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

Blacks were more likely to be diagnosed at a more advanced stage and to have squamous cell tumors, but were less likely to undergo surgery.

In multivariate regression controlling for age, sex, marital status, histology, and tumor location, black race was associated with worse survival.

When tumor status, surgery, and radiotherapy were added to the model, race was no longer significantly associated with survival.

While the disparity is due in part to differences in tumor histology, diagnosis at an earlier stage and higher rates of surgery among blacks could reduce this survival disparity.

[MeSH-major] Adenocarcinoma / ethnology. Carcinoma, Squamous Cell / ethnology. Esophageal Neoplasms / ethnology. Esophageal Neoplasms / therapy. Healthcare Disparities

Genetic Alliance. consumer health - Esophageal Cancer.

MedlinePlus Health Information. consumer health - Esophageal Cancer.

MedlinePlus Health Information. consumer health - Health Disparities.

[Email] Email this result item

Email the results to the following email address:   [X] Close

[CommentIn] Ann Surg Oncol. 2008 Mar;15(3):674-6 [18095032.001]

(PMID = 17987341.001).

[ISSN] 1534-4681

[Journal-full-title] Annals of surgical oncology

[ISO-abbreviation] Ann. Surg. Oncol.

[Language] eng

[Publication-type] Journal Article

[Publication-country] United States

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] HPV+ cervical carcinomas and cell lines display altered expression of caspases.

OBJECTIVE: Loss of expression of apoptotic regulatory proteins in many neoplasias might result in defective or delayed apoptosis, thus facilitating tumor growth or survival.

We analyzed here, the basal expression of precursors of apoptotic Caspases in normal cervical epithelium, HPV+ cervical tumor samples and HPV+ tumor-derived cell lines.

METHODS: Expression of initiator and effector Caspases was analyzed by immunochemistry in normal cervical epithelium and three types of cervical tumors (squamous cell carcinoma, adenocarcinoma and adenosquamous cell carcinoma) whereas expression of Caspases in HeLa, SiHa and CaSki cells was by immunofluorescence, Western blot and RT-PCR.

RESULTS: Expression of Caspases 3 and 9 was undetectable in adenocarcinoma and adenosquamous cell carcinoma, respectively.

Whereas in squamous cell carcinoma, the expression of Caspases was similar those observed in normal samples.

Expression of Caspases 3 and 6 was low in HeLa and CaSki cells, while Caspase 8 was low in SiHa and it was not detected in C33-A cells.

We did not observe an effect of the E6/E7 oncogenes on the expression of Caspases in C33-A cell.

CONCLUSION: Our results showed a differential expression of several Caspases in carcinoma samples and cell lines, suggesting multiple alterations of the Caspase pathways in cervical cancer.

[MeSH-major] Caspases / biosynthesis. Papillomavirus Infections / enzymology. Uterine Cervical Neoplasms / enzymology. Uterine Cervical Neoplasms / virology

[MeSH-minor] Adenocarcinoma / enzymology. Adenocarcinoma / pathology. Adenocarcinoma / virology. Blotting, Western. Carcinoma, Adenosquamous / enzymology. Carcinoma, Adenosquamous / pathology. Carcinoma, Adenosquamous / virology. Carcinoma, Squamous Cell / enzymology. Carcinoma, Squamous Cell / pathology. Carcinoma, Squamous Cell / virology. Cell Line, Tumor. Female. Fluorescent Antibody Technique. HeLa Cells. Human papillomavirus 16. Human papillomavirus 18. Humans. Immunohistochemistry. Isoenzymes / biosynthesis. Paraffin Embedding. Reverse Transcriptase Polymerase Chain Reaction

MedlinePlus Health Information. consumer health - Cervical Cancer.

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 17936882.001).

[ISSN] 1095-6859

[Journal-full-title] Gynecologic oncology

[ISO-abbreviation] Gynecol. Oncol.

[Language] eng

[Publication-type] Journal Article; Research Support, Non-U.S. Gov't

[Publication-country] United States

[Chemical-registry-number] 0 / Isoenzymes; EC 3.4.22.- / Caspases

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] Effect of EGFR antagonists gefitinib (Iressa) and C225 (Cetuximab) on MnSOD-plasmid liposome transgene radiosensitization of a murine squamous cell carcinoma cell line.

Radiation therapy of tumors of the head and neck region is compromised by dose limiting toxicity of normal tissues including the oral cavity and oropharyngeal mucosa.

MnSOD-Plasmid Liposome (MnSOD-PL) intraoral gene therapy has been demonstrated to decrease normal tissue toxicity and also improve survival in mice with orthotopic SCC-VII squamous cell tumors on the floor of the mouth.

Furthermore, intravenous administration of MnSOD-PL in mice with orthotopic tumors, or addition of MnSOD-PL to tumor cell lines in vitro produces a radiosensitizing effect attributable to differences in antioxidant pool responses of tumor cells compared to normal tissues following irradiation.

To determine whether EGF receptor (EGFR) antagonists Iressa, or Cetuximab provided further improvement of radiation killing of squamous cell tumors, MnSOD-PL transfected or control SCCVII tumor cells were irradiated in vitro, and then the effect of EGFR receptor antagonists was tested.

The results suggest some synergy of the effectiveness of the EGFR antagonist Iressa on increasing the radiation killing of SCC-VII cells that supplements MnSOD-PL tumor radiosensitization.

[MeSH-minor] Animals. Antibodies, Monoclonal, Humanized. Antineoplastic Agents / pharmacology. Carcinoma, Squamous Cell / genetics. Carcinoma, Squamous Cell / pathology. Cell Line, Tumor. Cell Survival / drug effects. Cell Survival / genetics. Cell Survival / radiation effects. Cetuximab. Dose-Response Relationship, Radiation. Liposomes. Mice. Transfection. Transgenes / genetics

COS Scholar Universe. author profiles.

Hazardous Substances Data Bank. CETUXIMAB .

NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .

NCI CPTC Antibody Characterization Program. NCI CPTC Antibody Characterization Program .

NCI CPTC Antibody Characterization Program. NCI CPTC Antibody Characterization Program .

[Email] Email this result item

Email the results to the following email address:   [X] Close

[ErratumIn] In Vivo. 2007 Nov-Dec;21(6):1172

(PMID = 17203769.001).

[ISSN] 0258-851X

[Journal-full-title] In vivo (Athens, Greece)

[ISO-abbreviation] In Vivo

[Language] eng

[Publication-type] Journal Article

[Publication-country] Greece

[Chemical-registry-number] 0 / Antibodies, Monoclonal; 0 / Antibodies, Monoclonal, Humanized; 0 / Antineoplastic Agents; 0 / Liposomes; 0 / Quinazolines; EC 1.15.1.1 / Superoxide Dismutase; EC 2.7.10.1 / Receptor, Epidermal Growth Factor; PQX0D8J21J / Cetuximab; S65743JHBS / gefitinib

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] Neuroendocrine tumors and their association with rare tumors: observation of 4 cases.

PURPOSE: Neuroendocrine tumors are rare neoplasms, with an incidence of about 1/100,000/year.

The association between digestive neuroendocrine tumors and epithelial tumors is known, accounting for about 10% of cases, whilst in a very small number of other cases an association with other low incidence tumors has been observed.

METHODS: During the past 19 years the Rare Hormonal Tumors Group of the Istituti Ospitalieri in Cremona, Italy has observed 300 patients affected by neuroendocrine tumors.

We report here on four cases in which there was an unusual association with other rare neoplasms.

RESULTS: Overall, four of the 300 observed cases (1.3%) showed an unusual association with rare nonepithelial neoplasms:.

(2) Merkel cell tumor and squamous cell carcinoma of the skin;.

(3) medullary thyroid carcinoma, yolk sac tumor of the testis and gastrointestinal stromal tumor (GIST);.

(4) gastric carcinoid and gastrointestinal stromal tumor (GIST).

DISCUSSION: There cases are of interest not only from an epidemiological point of view, but also offer insight into possible geno-phenotypical implications.

The c-kit expression, typical of GISTs but observed also in other epithelial and neuroendocrine tumors, not only broadens the possibility to gain insight into the carcinogenesis of these neoplasms, but also opens the field to possible new therapeutic opportunities using multitargeted molecules.

The contemporaneous presence of other lesions, such as the Merkel cell tumor and the squamous cell carcinoma of the skin can be interpreted as an answer by the cell to the same mutagenic stimulus.

In other cases, where a possible link is not yet found which could explain the synchronism or metachronism of low incidence neoplasms, it remains possible that the associations are entirely coincidental.

We await for new instruments which could help us demonstrate the possible relationships between low incidence neoplasms.

[MeSH-major] Neoplasms / pathology. Neuroendocrine Tumors / pathology

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 20707247.001).

[ISSN] 1128-3602

[Journal-full-title] European review for medical and pharmacological sciences

[ISO-abbreviation] Eur Rev Med Pharmacol Sci

[Language] eng

[Publication-type] Case Reports; Journal Article; Research Support, Non-U.S. Gov't

[Publication-country] Italy

[Chemical-registry-number] EC 2.7.10.1 / Proto-Oncogene Proteins c-kit

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

BACKGROUND & OBJECTIVE: EMS1 (chromosome eleven, band q13, mammary tumor and squamous cell carcinoma-associated gene 1) is correlated to the genesis, progression, invasion and metastasis of some malignancies.

METHODS: The expression of EMS1 protein in 20 specimens of normal gastric mucosa, 38 specimens of intraepithelial neoplasia, and 146 specimens of gastric carcinoma was detected by immunohistochemistry.

The positive rate of EMS1 protein was significantly higher in gastric carcinoma than in intraepithelial neoplasia and normal gastric mucosa (89.7% vs. 68.4% and 20.0%, P<0.001), and significantly higher in intraepithelial neoplasia than in normal gastric mucosa (P<0.001).

EMS1 protein expression had no correlations to sex, age, tumor differentiation and diameter.

[MeSH-major] Cortactin / genetics. Stomach Neoplasms / genetics

[MeSH-minor] Adult. Aged. Female. Humans. Immunohistochemistry. Lymphatic Metastasis. Male. Middle Aged. Neoplasm Staging

MedlinePlus Health Information. consumer health - Stomach Cancer.

NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 18334127.001).

[Journal-full-title] Ai zheng = Aizheng = Chinese journal of cancer

[ISO-abbreviation] Ai Zheng

[Language] chi

[Publication-type] English Abstract; Journal Article; Research Support, Non-U.S. Gov't

[Publication-country] China

[Chemical-registry-number] 0 / CTTN protein, human; 0 / Cortactin

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] Application of lateral arm free flap in oral and maxillofacial reconstruction following tumor surgery.

Sixteen LAFF were harvested to reconstruct defects caused by the dissection of malignant tumors of the oral and maxillofacial regions.

The tumor was squamous cell carcinoma of the tongue (6 cases), floor of the mouth (4), retromolar area (3), inner cheek (2), and lower gingival (1).

[MeSH-major] Carcinoma, Squamous Cell / surgery. Mouth Neoplasms / surgery. Reconstructive Surgical Procedures / methods. Surgical Flaps

MedlinePlus Health Information. consumer health - Oral Cancer.

[Email] Email this result item

Email the results to the following email address:   [X] Close

[Copyright] 2007 S. Karger AG, Basel

(PMID = 17709930.001).

[ISSN] 1423-0151

[Journal-full-title] Medical principles and practice : international journal of the Kuwait University, Health Science Centre

[ISO-abbreviation] Med Princ Pract

[Language] eng

[Publication-type] Journal Article

[Publication-country] Switzerland

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] High-resolution mapping of tumor redox status by magnetic resonance imaging using nitroxides as redox-sensitive contrast agents.

The levels of 3CP were examined by EPRI and MRI for differences in reduction between muscle and tumor (squamous cell carcinoma) implanted in the hind leg of C3H mice simultaneously.

The tumor regions exhibited a faster decay rate of the nitroxide compared to muscle (0.097 min(-1) versus 0.067 min(-1), respectively).

[MeSH-major] Magnetic Resonance Imaging / methods. Neoplasms, Experimental / pathology. Nitrogen Oxides / chemistry

[MeSH-minor] Animals. Carcinoma, Squamous Cell / metabolism. Carcinoma, Squamous Cell / pathology. Cyclic N-Oxides / chemistry. Cyclic N-Oxides / metabolism. Electron Spin Resonance Spectroscopy / methods. Female. Mice. Mice, Inbred C3H. Models, Chemical. Muscles / metabolism. Oxidation-Reduction. Pyrrolidines / chemistry. Pyrrolidines / metabolism

MedlinePlus Health Information. consumer health - MRI Scans.

COS Scholar Universe. author profiles.

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 16638852.001).

[ISSN] 1078-0432

[Journal-full-title] Clinical cancer research : an official journal of the American Association for Cancer Research

[ISO-abbreviation] Clin. Cancer Res.

[Language] eng

[Grant] United States / Intramural NIH HHS / / Z01 NS003047-01

[Publication-type] Comparative Study; Journal Article; Research Support, N.I.H., Intramural

[Publication-country] United States

[Chemical-registry-number] 0 / Cyclic N-Oxides; 0 / Nitrogen Oxides; 0 / Pyrrolidines; 14332-28-6 / nitroxyl; 4399-80-8 / 3-carbamoyl-2,2,5,5-tetramethyl-1-pyrrolidinyl-N-oxyl

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] Oxford experience with neoadjuvant chemotherapy and surgical resection for esophageal adenocarcinomas and squamous cell tumors.

Since February 2000 it has been our practice to offer this chemotherapy regime to patients with T2 and T3 or T1N1 tumors.

Six patients (5.7%) had progressive disease and were inoperable (discovered in four at surgery).

A total of 182 patients with a median age of 63 (range 30-80), 41 squamous and 141 adenocarcinomas underwent surgery.

A radical surgical approach to the primary tumor in combination with OEO2 neoadjuvant chemotherapy has led to a high R0 resection rate and good survival with acceptable morbidity and mortality.

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 18430099.001).

[ISSN] 1442-2050

[Journal-full-title] Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus

[ISO-abbreviation] Dis. Esophagus

[Language] ENG

[Publication-type] Journal Article

[Publication-country] United States

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] Immunolabeling pattern of podoplanin (d2-40) may distinguish basal cell carcinomas from trichoepitheliomas: a clinicopathologic and immunohistochemical study of 49 cases.

When the morphologic distinction between basal cell carcinomas (BCCs) and tichoepitheliomas is unclear, it poses a rare diagnostic challenge as the commonly defined histologic criterion is insufficient for differentiating these two neoplasms from each other.

Their distinction is clinically important because the risk of progressive disease in BCC can be problematic, and trichoepitheliomas misinterpreted as BCC burdens the patient with an inaccurate diagnosis and consequential inappropriate surgery.

Podoplanin (D2-40) is a well-known lymphatic endothelial surface marker that has been postulated to be upregulated in the outer root sheath of hair follicles and cutaneous neoplasms, such as adnexal tumors, squamous cell carcinomas, etc.

We studied the expression of D2-40 by immunohistochemistry to determine if this marker could reliably differentiate these neoplasms from each other.

A total of 49 cutaneous tumors, including 22 cases of trichoepitheliomas and 27 cases of BCC were examined.

This data suggests that D2-40 expression could be a useful potential marker to distinguish BCCs from trichoepitheliomas, especially when there is a high index of histologic suspicion for either of these two tumors.

[MeSH-major] Biomarkers, Tumor / analysis. Carcinoma, Basal Cell / diagnosis. Membrane Glycoproteins / biosynthesis. Neoplasms, Basal Cell / diagnosis. Skin Neoplasms / diagnosis

[MeSH-minor] Antibodies, Monoclonal. Antibodies, Monoclonal, Murine-Derived. Diagnosis, Differential. Humans. Immunohistochemistry. Predictive Value of Tests

MedlinePlus Health Information. consumer health - Skin Cancer.

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 20559122.001).

[ISSN] 1533-0311

[Journal-full-title] The American Journal of dermatopathology

[ISO-abbreviation] Am J Dermatopathol

[Language] eng

[Publication-type] Journal Article

[Publication-country] United States

[Chemical-registry-number] 0 / Antibodies, Monoclonal; 0 / Antibodies, Monoclonal, Murine-Derived; 0 / Biomarkers, Tumor; 0 / Membrane Glycoproteins; 0 / PDPN protein, human; 0 / monoclonal antibody D2-40

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] Searching for molecular markers in head and neck squamous cell carcinomas (HNSCC) by statistical and bioinformatic analysis of larynx-derived SAGE libraries.

BACKGROUND: Head and neck squamous cell carcinoma (HNSCC) is one of the most common malignancies in humans.

When detected early, HNSCC has a good prognosis, but most patients present metastatic disease at the time of diagnosis, which significantly reduces survival rate.

METHODS: Aiming to identify differentially-expressed genes involved in laryngeal squamous cell carcinoma (LSCC) development and progression, we generated individual Serial Analysis of Gene Expression (SAGE) libraries from a metastatic and non-metastatic larynx carcinoma, as well as from a normal larynx mucosa sample.

RESULTS: Statistical data analysis identified a subset of 1,216 differentially expressed tags between tumor and normal libraries, and 894 differentially expressed tags between metastatic and non-metastatic carcinomas.

Consistent with our statistical analysis, quantitative PCR confirmed the upregulation of BST2 and MFAP2 and the downregulation of KRT31 when samples of HNSCC were compared to tumor-free surgical margins.

As expected, GNA15 presented a non-significant differential expression pattern when tumor samples were compared to normal tissues.

CONCLUSION: To the best of our knowledge, this is the first study reporting SAGE data in head and neck squamous cell tumors.

This result suggests the existence of potential common biomarkers for prognosis and targeted-therapy development in this heterogeneous type of tumor.

COS Scholar Universe. author profiles.

[Email] Email this result item

Email the results to the following email address:   [X] Close

[Cites] CA Cancer J Clin. 2005 Mar-Apr;55(2):74-108 [15761078.001]

[Cites] Oncogene. 2005 Feb 10;24(7):1244-51 [15558013.001]

[Cites] Int J Cancer. 2005 Feb 20;113(5):789-97 [15499618.001]

[Cites] Nat Rev Cancer. 2005 Feb;5(2):127-35 [15685196.001]

[Cites] Nat Genet. 2005 Feb;37(2):182-6 [15640797.001]

[Cites] Physiol Genomics. 2002 Oct 29;11(2):37-44 [12407185.001]

[Cites] Nucleic Acids Res. 2001 May 1;29(9):e45 [11328886.001]

[Cites] J Cell Biol. 2001 Aug 6;154(3):619-30 [11489919.001]

[Cites] Head Neck. 2001 Mar;23(3):238-53 [11428456.001]

[Cites] Br J Dermatol. 2001 May;144(5):977-82 [11359384.001]

[Cites] Bioinformatics. 2000 Nov;16(11):953-9 [11159306.001]

[Cites] J Cell Biol. 2000 Aug 21;150(4):921-8 [10953016.001]

[Cites] Oncogene. 2000 Jun 29;19(28):3220-4 [10918578.001]

[Cites] Laryngoscope. 2000 Mar;110(3 Pt 1):374-81 [10718422.001]

[Cites] Mol Cancer Ther. 2005 Jan;4(1):151-68 [15657362.001]

[Cites] Arch Otolaryngol Head Neck Surg. 2005 Jan;131(1):10-8 [15655179.001]

[Cites] Clin Cancer Res. 2004 Dec 15;10(24):8442-50 [15623624.001]

[Cites] Cancer. 2004 Dec 15;101(12):2779-87 [15546137.001]

[Cites] Curr Cancer Drug Targets. 2004 Dec;4(8):637-51 [15578920.001]

[Cites] Blood. 2004 Dec 1;104(12):3697-704 [15292061.001]

[Cites] Cancer Res. 2004 Nov 1;64(21):7787-93 [15520184.001]

[Cites] Biochem Biophys Res Commun. 1999 May 19;258(3):583-91 [10329429.001]

[Cites] Nat Genet. 1996 Dec;14(4):457-60 [8944026.001]

[Cites] Science. 1995 Oct 20;270(5235):484-7 [7570003.001]

[Cites] J Biol Chem. 1994 May 20;269(20):14661-5 [7514177.001]

[Cites] Nature. 1993 Dec 2;366(6454):473-5 [7902537.001]

[Cites] Int J Cancer. 2004 Nov 1;112(2):249-58 [15352037.001]

[Cites] Med Electron Microsc. 2004 Jun;37(2):89-96 [15221650.001]

[Cites] Proc Natl Acad Sci U S A. 2004 Jun 22;101(25):9309-14 [15184677.001]

[Cites] Cell Mol Life Sci. 2004 Jun;61(11):1372-83 [15170515.001]

[Cites] Oncogene. 2004 Apr 1;23(14):2484-98 [14676830.001]

[Cites] Arch Otolaryngol Head Neck Surg. 2004 Mar;130(3):295-302 [15023835.001]

[Cites] Oral Oncol. 2004 Apr;40(4):418-26 [14969821.001]

[Cites] Cancer Res. 2004 Jan 1;64(1):55-63 [14729608.001]

[Cites] Oncogene. 2003 Sep 29;22(42):6598-608 [14528285.001]

[Cites] Int J Mol Med. 2003 Oct;12(4):429-35 [12964014.001]

[Cites] Clin Cancer Res. 2003 Aug 1;9(8):3058-64 [12912957.001]

[Cites] Arch Otolaryngol Head Neck Surg. 2003 Jul;129(7):760-70 [12874079.001]

[Cites] Arch Otolaryngol Head Neck Surg. 2003 Jul;129(7):754-9 [12874078.001]

[Cites] Int J Cancer. 2003 Sep 20;106(5):683-9 [12866027.001]

[Cites] Oral Oncol. 2003 Apr;39(3):259-68 [12618198.001]

[Cites] Oral Oncol. 2003 Apr;39(3):248-58 [12618197.001]

[Cites] Eur J Oral Sci. 2003 Feb;111(1):34-41 [12558806.001]

[Cites] Physiol Genomics. 2003 Jan 15;12(2):159-62 [12429865.001]

[Cites] Oncogene. 2002 Nov 21;21(53):8206-19 [12444558.001]

[Cites] Biol Direct. 2008;3:22 [18513408.001]

[Cites] Cancer. 2002 Oct 1;95(7):1482-94 [12237917.001]

[Cites] Head Neck. 2002 Sep;24(9):874-87 [12211052.001]

[Cites] Leukemia. 2002 Sep;16(9):1713-24 [12200686.001]

[Cites] Genome Biol. 2002 Jun 18;3(7):RESEARCH0034 [12184808.001]

[Cites] Nat Rev Cancer. 2002 Mar;2(3):210-9 [11990857.001]

[Cites] Oncogene. 2002 Apr 18;21(17):2634-40 [11965536.001]

[Cites] Cell Growth Differ. 2002 Apr;13(4):163-71 [11971816.001]

[Cites] Cancer Res. 2002 Feb 15;62(4):1184-90 [11861402.001]

[Cites] Oncogene. 2001 Sep 27;20(43):6196-204 [11593428.001]

[Cites] CA Cancer J Clin. 2001 Jan-Feb;51(1):15-36 [11577478.001]

[Cites] Hum Mol Genet. 2001 Sep 15;10(19):2133-41 [11590130.001]

[Cites] Cell Oncol. 2008;30(1):63-75 [18219111.001]

[Cites] Oncogene. 2007 Mar 22;26(13):1971-82 [17043662.001]

[Cites] Biol Cell. 2006 Aug;98(8):479-90 [16608439.001]

[Cites] Cancer Lett. 2006 Jul 28;239(1):136-43 [16181731.001]

[Cites] FEBS Lett. 2006 May 22;580(12):2860-8 [16574107.001]

[Cites] Cancer Res. 2006 Apr 15;66(8):4182-90 [16618740.001]

[Cites] J Biol Chem. 2006 Apr 14;281(15):10089-97 [16492672.001]

[Cites] CA Cancer J Clin. 2006 Mar-Apr;56(2):106-30 [16514137.001]

[Cites] Blood. 2006 Mar 15;107(6):2223-33 [16291593.001]

[Cites] Oral Oncol. 2006 Mar;42(3):306-16 [16321566.001]

[Cites] Blood. 2006 Feb 15;107(4):1570-81 [16249385.001]

[Cites] Lab Invest. 2005 Aug;85(8):1024-39 [16205657.001]

[Cites] Mol Cancer Ther. 2005 Jun;4(6):865-75 [15956244.001]

[Cites] Oral Oncol. 2005 Apr;41(4):365-74 [15792608.001]

(PMID = 19014460.001).

[ISSN] 1755-8794

[Journal-full-title] BMC medical genomics

[ISO-abbreviation] BMC Med Genomics

[Language] eng

[Publication-type] Journal Article

[Publication-country] England

[Other-IDs] NLM/ PMC2629771

[Investigator] Curry PM; de Carvalho MB; Dias-Neto E; Figueiredo DL; Fukuyama EE; Góis-Filho JF; Leopoldino AM; Mamede RC; Michaluart-Junior P; Moreira-Filho CA; Moyses RA; Nóbrega FG; Nóbrega MP; Nunes FD; Ojopi EP; Okamoto OK; Serafini LN; Severino P; Silva AM; Silva WA Jr; Silveira NJ; Souza SC; Tajara EH; Wünsch-Filho V; Zago MA; Amar A; Arap SS; Araújo NS; Araújo-Filho V; Barbieri RB; Bandeira CM; Bastos AU; Braconi MA; Brandão LG; Brandão RM; Canto AL; Carmona-Raphe J; Carvalho-Neto PB; Casemiro AF; Cerione M; Cernea CR; Cicco R; Chagas MJ; Chedid H; Chiappini PB; Correia LA; Costa A; Costa AC; Cunha BR; Curioni OA; Dias TH; Durazzo M; Ferraz AR; Figueiredo RO; Fortes CS; Franzi SA; Frizzera AP; Gallo J; Gazito D; Guimarães PE; Gutierres AP; Inamine R; Kaneto CM; Lehn CN; López RV; Macarenco R; Magalhães RP; Martins AE; Meneses C; Mercante AM; Montenegro FL; Pinheiro DG; Polachini GM; Porsani AF; Rapoport A; Rodini CO; Rodrigues AN; Rodrigues-Lisoni FC; Rodrigues RV; Rossi L; Santos AR; Santos M; Settani F; Silva FA; Silva IT; Silva-Filho GB; Smith RB; Souza TB; Stabenow E; Takamori JT; Tavares MR; Turcano R; Valentim PJ; Vidotto A; Volpi EM; Xavier FC; Yamagushi F; Cominato ML; Correa PM; Mendes GS; Paiva R; Ramos O; Silva C; Silva MJ; Tarlá MV

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

SUBJECT: Oral cavity cancers represent 30% of the cephalic extremity tumors.

The patients benefited from a surgical resection of the tumor by respecting the safety margins, with an immediate reconstruction allowing the restoring of the oral functions.

The majority of tumors were squamous cell carcinomas (50 cases).

As complications, we noted one complete necrosis and two partial necrosis of the flap, two postoperative wound complications with dehiscence as well as a massive local recurrence of initial tumor in one patient.

[MeSH-major] Mouth Neoplasms / surgery. Neoplasm Recurrence, Local. Postoperative Complications. Reconstructive Surgical Procedures / methods. Surgical Flaps

MedlinePlus Health Information. consumer health - After Surgery.

MedlinePlus Health Information. consumer health - Oral Cancer.

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 15896896.001).

[ISSN] 0294-1260

[Journal-full-title] Annales de chirurgie plastique et esthétique

[ISO-abbreviation] Ann Chir Plast Esthet

[Language] fre

[Publication-type] English Abstract; Journal Article

[Publication-country] France

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] Expression of 14-3-3sigma, p16 and p53 proteins in anal squamous intraepithelial neoplasm and squamous cell carcinoma.

14-3-3sigma is a p53-regulated G2/M inhibitor involved in numerous cellular signaling pathways related to cell cycle, DNA repair and apoptosis.

Recent studies have showed that 14-3-3sigma was silenced transcriptionally through promoter hypermethylation mainly in HPV-negative vulvar squamous cell carcinoma (SCC).

However, the expression of 14-3-3sigma protein has not yet been studied in anal SCC and its precursor, anal intraepithelial neoplasm (AIN).

In this study, we evaluated the expression of 14-3-3sigma, p16 and p53 in 34 cases of normal perianal squamous mucosa, 5 cases of squamous hyperplasia and 62 cases of AIN, including 54 bowenoid and 8 differentiated AINs.

Expression of p16, p53 and 14-3-3sigma proteins was not seen in normal squamous epithelium.

Weak staining for 14-3-3sigma was seen in anal squamous hyperplasia.

NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .

NCI CPTC Antibody Characterization Program. NCI CPTC Antibody Characterization Program .

[Email] Email this result item

Email the results to the following email address:   [X] Close

[Cites] Am J Surg Pathol. 2000 Mar;24(3):429-41 [10716158.001]

[Cites] Oncogene. 2000 Nov 2;19(46):5298-302 [11077447.001]

[Cites] J Low Genit Tract Dis. 2007 Jan;11(1):46-7 [17194951.001]

[Cites] Curr Opin Oncol. 2006 Sep;18(5):463-8 [16894294.001]

[Cites] Cancer Res. 2000 Aug 15;60(16):4353-7 [10969776.001]

[Cites] Proc Natl Acad Sci U S A. 2000 May 23;97(11):6049-54 [10811911.001]

[Cites] Anticancer Res. 2006 Jul-Aug;26(4B):3105-10 [16886641.001]

[Cites] Am J Surg Pathol. 2006 Jul;30(7):795-801 [16819320.001]

[Cites] Semin Cancer Biol. 2006 Jun;16(3):183-92 [16697662.001]

[Cites] Semin Cancer Biol. 2006 Jun;16(3):225-34 [16697215.001]

[Cites] Semin Cancer Biol. 2006 Jun;16(3):161 [16697214.001]

[Cites] Mol Cell Proteomics. 2005 Jun;4(6):785-95 [15778465.001]

[Cites] Histopathology. 2005 Jun;46(6):718-20 [15910611.001]

[Cites] J Low Genit Tract Dis. 2005 Apr;9(2):108-13 [15870532.001]

[Cites] Cell Res. 2005 Apr;15(4):228-36 [15857577.001]

[Cites] Pathol Int. 2005 Feb;55(2):77-82 [15693853.001]

[Cites] AIDS Read. 2005 Feb;15(2):79-82, 85-6, 88, 91 [15712398.001]

[Cites] Hum Pathol. 2004 Dec;35(12):1477-83 [15619206.001]

[Cites] Int J Oncol. 2004 Dec;25(6):1591-7 [15547695.001]

[Cites] Semin Cancer Biol. 1998;8(5):345-57 [10101800.001]

[Cites] Mol Cell. 1997 Dec;1(1):3-11 [9659898.001]

[Cites] J Natl Cancer Inst. 1994 Nov 16;86(22):1711-6 [7966400.001]

[Cites] Pathol Int. 2004 Oct;54(10):743-50 [15482563.001]

[Cites] Br J Cancer. 2004 Sep 13;91(6):1131-8 [15292943.001]

[Cites] Int J Gynecol Pathol. 2004 Jul;23(3):206-14 [15213596.001]

[Cites] Clin Cancer Res. 2004 Apr 15;10(8):2687-93 [15102672.001]

[Cites] Nat Rev Cancer. 2003 Dec;3(12):931-43 [14737123.001]

[Cites] Oncogene. 2002 Mar 14;21(12):1876-81 [11896620.001]

[Cites] J Biol Chem. 2001 Nov 30;276(48):45193-200 [11577088.001]

[Cites] Int J Gynecol Pathol. 2001 Jan;20(1):16-30 [11192069.001]

[Cites] Br J Dermatol. 2007 Sep;157(3):523-30 [17573882.001]

(PMID = 18787619.001).

[ISSN] 1936-2625

[Journal-full-title] International journal of clinical and experimental pathology

[ISO-abbreviation] Int J Clin Exp Pathol

[Language] eng

[Publication-type] Journal Article

[Publication-country] United States

[Other-IDs] NLM/ PMC2480570

[Keywords] NOTNLM ; 14-3-3σ / AIN / Anal intraepithelial neoplasm / Bowenoid / differentiated / p16 / p53 / simplex

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

The median age was 49.8 years; all but 1 tumor were squamous cell carcinomas.

Ten (83.3%) had pelvic and systemic disease, whereas only 2 had systemic disease alone.

A single patient having metastatic disease in the lung showed stabilization for 6 months to then progressing in bone.

Despite lack of activity of single-agent imatinib, further studies in cervical cancer are deserved to better define the status of imatinib targets in this tumor and to investigate its activity in combination with cytotoxic drugs.

[MeSH-major] Carcinoma, Squamous Cell / drug therapy. Piperazines / therapeutic use. Pyrimidines / therapeutic use. Receptor, Platelet-Derived Growth Factor alpha / metabolism. Uterine Cervical Neoplasms / drug therapy

[MeSH-minor] Adult. Aged. Antineoplastic Agents / adverse effects. Antineoplastic Agents / therapeutic use. Benzamides. Chemotherapy, Adjuvant. Female. Humans. Imatinib Mesylate. Middle Aged. Neoplasm Metastasis. Recurrence. Survival Analysis. Treatment Outcome

Genetic Alliance. consumer health - Cervical cancer.

Genetic Alliance. consumer health - Metastatic cancer.

MedlinePlus Health Information. consumer health - Cervical Cancer.

International Agency for Research on Cancer - Screening Group. diagnostics - Histopathology and cytopathology of the uterine cervix - digital atlas .

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 19955950.001).

[ISSN] 1525-1438

[Journal-full-title] International journal of gynecological cancer : official journal of the International Gynecological Cancer Society

[ISO-abbreviation] Int. J. Gynecol. Cancer

[Language] eng

[Publication-type] Clinical Trial; Journal Article; Research Support, Non-U.S. Gov't

[Publication-country] United States

[Chemical-registry-number] 0 / Antineoplastic Agents; 0 / Benzamides; 0 / Piperazines; 0 / Pyrimidines; 8A1O1M485B / Imatinib Mesylate; EC 2.7.10.1 / Receptor, Platelet-Derived Growth Factor alpha

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] Prepubertal testicular tumors: frequently overlooked.

OBJECTIVE: Prepubertal testicular tumors are fundamentally distinct from their adult counterparts.

MATERIAL AND METHODS: A retrospective review was performed of all testicular tumors diagnosed between 1996 and 2006 in males younger than 14 years.

RESULTS: Of 15 primary testicular tumors, eight (53%) were germ-cell tumors (three teratomas, two yolk sac tumors, one seminoma, one embryonic carcinoma and one choriocarcinoma), four (27%) tumor-like lesions (epidermoid cysts), two (13%) gonadal stromal tumors (a Leydig and a Sertoli cell tumor), and one (7%) gonadoblastoma with gonadal dysgenesis.

All boys were presented with a painless scrotal mass and four (27%) of them with elevated tumor markers.

At a mean 4-year follow-up no patient has presented with recurrent tumor in the residual or contralateral testicle.

Postoperative physical examination and scrotal ultrasound were obtained in 14 patients at a median follow-up of 48.2 months, and there was no evidence of tumor progression.

CONCLUSIONS: Benign teratoma and epidermoid cysts were the most common prepubertal testicular tumors.

Any suspicion of a testicular tumor warrants an inguinal approach to prevent scrotal violation of the tumor.

Our limited experience with testis-sparing procedures supports the current trends that organ-confined surgery should be performed for benign lesions such as teratoma, Leydig cell tumor and epidermoid cysts based on frozen biopsy findings.

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 18947799.001).

[ISSN] 1873-4898

[Journal-full-title] Journal of pediatric urology

[ISO-abbreviation] J Pediatr Urol

[Language] eng

[Publication-type] Journal Article

[Publication-country] England

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

[Title] The prognostic role of clinical, morphological and molecular markers in oral squamous cell tumors.

Despite of considerable advances in the diagnostic and therapeutic possibilities, the prognosis of epithelial tumors in the oral cavity is still very poor.

These factors may be linked to the patient (e.g. age, sex, general condition and immunological parameters) or to the tumor localization.

A survey of the literature reveals that the TNM stage, the grade, the mode of invasion and the depth of the tumor infiltration are generally the most important factors influencing the fate of the patient.

The prognosis depends primarily on the clinicopathological parameters, though even if they are known, it is not possible to screen out those patients who are at particular risk of a relapse.

[MeSH-major] Biomarkers, Tumor / analysis. Carcinoma, Squamous Cell / pathology. Mouth Neoplasms / pathology. Neoplasm Staging

[MeSH-minor] Cell Membrane / chemistry. Genes, Tumor Suppressor. Humans. Immunohistochemistry. Male. Oncogenes. Prognosis. Survival

MedlinePlus Health Information. consumer health - Oral Cancer.

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 15800706.001).

[ISSN] 0028-2685

[Journal-full-title] Neoplasma

[ISO-abbreviation] Neoplasma

[Language] eng

[Publication-type] Journal Article; Review

[Publication-country] Slovakia

[Chemical-registry-number] 0 / Biomarkers, Tumor

[Number-of-references] 74

   

[Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.

Mice that received no cream treatment and were exposed to increasing levels of SSL showed significant SSL exposure-dependent decreases in survival and significant increases in the in-life observations of skin lesion onset, incidence, and multiplicity, and significant SSL exposure-dependent increases in the incidences and multiplicities of histopathology-determined squamous cell nonneoplastic skin lesions (squamous hyperplasia and focal atypical hyperplasia) and squamous cell neoplasms (papilloma, carcinoma in situ, and/or carcinoma).

Squamous cell neoplasms were not detected in mice that received no SSL exposure.

The topical treatment with the control cream of mice that were exposed to SSL did not impart a measurable effect when compared with comparable measurements in mice that received no cream treatment and were exposed to the same level of SSL, suggesting that the control cream used in these studies did not alter the efficiency of the SSL delivered to mice or the tolerability of mice to SSL.

The administration of aloe gel creams to male mice had no effect on the incidences or multiplicities of histopathology-determined squamous cell nonneoplastic skin lesions or neoplasms.

Female mice treated with aloe gel creams (3% and 6%) had significantly increased multiplicities of squamous cell neoplasms.

In male mice exposed to SSL and treated with the 6% whole leaf cream, a significant increase was observed in the multiplicity of squamous cell neoplasms.

Female mice exposed to SSL and treated with the 3% whole leaf creams had significantly decreased multiplicity of squamous cell nonneoplastic lesions and significantly increased multiplicity of squamous cell neoplasms.

Female mice exposed to SSL and treated with the 6% whole leaf cream had significantly decreased multiplicity of squamous cell nonneoplastic lesions.

Male mice administered the 3% decolorized whole leaf cream had significantly increased multiplicity of squamous cell neoplasms.

Female mice administered the 3% decolorized whole leaf cream had significantly decreased multiplicity of squamous cell nonneoplastic skin lesions and significantly increased multiplicity of squamous cell neoplasms.

In female mice that received the 6% decolorized whole leaf cream, there was a significant increase in the multiplicity of squamous cell neoplasms.

The administration of aloe-emodin creams to male mice had no effect on the incidence or multiplicity of histopathology-determined nonneoplastic skin lesions or squamous cell neoplasms.

Female mice treated with the 74.6 µg/g aloe-emodin cream had significantly decreased multiplicity of histopathology-determined squamous cell nonneoplastic skin lesions and significantly increased multiplicity of squamous cell neoplasms.

ALOE GEL OR ALOE-EMODIN: under the conditions of these studies, there was a weak enhancing effect of aloe gel or aloe-emodin on the photocarcinogenic activity of SSL in female but not in male SKH-1 mice based on an increase in the multiplicity of histopathologically-determined squamous cell neoplasms.

ALOE WHOLE LEAF OR DECOLORIZED WHOLE LEAF: under the conditions of these studies, there was a weak enhancing effect of aloe whole leaf or decolorized whole leaf on the photocarcinogenic activity of SSL in both male and female SKH-1 mice based on an increase in the multiplicity of histopathologically-determined squamous cell neoplasms.

[MeSH-major] Aloe / toxicity. Plant Extracts / toxicity. Skin Neoplasms / etiology. Sunlight / adverse effects

[Email] Email this result item

Email the results to the following email address:   [X] Close

(PMID = 21031007.001).

[ISSN] 0888-8051

[Journal-full-title] National Toxicology Program technical report series

[ISO-abbreviation] Natl Toxicol Program Tech Rep Ser

[Language] eng

[Publication-type] Journal Article; Technical Report

[Publication-country] United States

[Chemical-registry-number] 0 / Plant Extracts