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Items 1 to 14 of about 14
1. Shirataki Y, Tani S, Sakagami H, Satoh K, Nakashima H, Gotoh K, Motohashi N: Relationship between cytotoxic activity and radical intensity of isoflavones from Sophora species. Anticancer Res; 2001 Jul-Aug;21(4A):2643-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Among 11 isoflavones tested, genistein [YS13] produced higher cytotoxic activity against human oral tumor cell lines (HSC-2, HSG) than against normal cells (human gingival fibroblast, HGF), suggesting its tumor-specific action.
  • Addition of two prenyl groups produced YS21 with the highest cytotoxic activity but lower tumor-specificity.
  • These data suggest the medicinal efficacy of isoflavones.
  • [MeSH-major] Anti-HIV Agents / pharmacology. Anti-Infective Agents / pharmacology. Antineoplastic Agents / toxicity. Isoflavones / toxicity
  • [MeSH-minor] Animals. Anti-Bacterial Agents. Carcinoma, Squamous Cell / drug therapy. Cattle. Drug Screening Assays, Antitumor. Fibroblasts / cytology. Fibroblasts / drug effects. Free Radical Scavengers / chemistry. Free Radical Scavengers / pharmacology. Gingiva / cytology. Gingiva / drug effects. HIV / drug effects. Helicobacter pylori / drug effects. Humans. Mouth Neoplasms / drug therapy. Salivary Gland Neoplasms / drug therapy. Structure-Activity Relationship. Superoxides / metabolism

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  • (PMID = 11724333.001).
  • [ISSN] 0250-7005
  • [Journal-full-title] Anticancer research
  • [ISO-abbreviation] Anticancer Res.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Greece
  • [Chemical-registry-number] 0 / Anti-Bacterial Agents; 0 / Anti-HIV Agents; 0 / Anti-Infective Agents; 0 / Antineoplastic Agents; 0 / Free Radical Scavengers; 0 / Isoflavones; 11062-77-4 / Superoxides
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2. Kawase M, Sakagami H, Furuya K, Kikuchi H, Nishikawa H, Motohashi N, Morimoto Y, Varga A, Molnár J: Cell death-inducing activity of opiates in human oral tumor cell lines. Anticancer Res; 2002 Jan-Feb;22(1A):211-4
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • In screening cytotoxic agents in morphine alkaloids [TE1-10], codeinone [TE8] was cytotoxic against two human oral tumor cells lines (HSC-2 and HSG).
  • Human oral gingival fibroblasts (HGF) were relatively resistant to codeinone, as judged by higher SI ratio (3.7) suggesting the tumor-selective cytotoxicity of codeinone.
  • The cytotoxic activity of morphine (CC50=221 microg/mL) against HSC-2 was slightly lower than that of codeine (CC50=186 microg/mL), thebaine (CC50=125 microg/mL), etorphine (CC50=94 microg/mL) or dihydroetorphine (CC50=60 microg/mL).
  • [MeSH-major] Carcinoma, Squamous Cell / drug therapy. Codeine / analogs & derivatives. Morphine Derivatives / toxicity. Salivary Gland Neoplasms / drug therapy
  • [MeSH-minor] Animals. Cell Death / drug effects. Child. Drug Resistance, Multiple. Female. Fibroblasts / cytology. Fibroblasts / drug effects. Fibroblasts / metabolism. Gingiva / cytology. HL-60 Cells / cytology. HL-60 Cells / drug effects. HL-60 Cells / metabolism. Humans. Leukemia L5178 / drug therapy. Leukemia L5178 / genetics. Leukemia L5178 / metabolism. Leukemia L5178 / pathology. Mice. P-Glycoprotein / biosynthesis. P-Glycoprotein / genetics. Structure-Activity Relationship. Transfection

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  • (PMID = 12017290.001).
  • [ISSN] 0250-7005
  • [Journal-full-title] Anticancer research
  • [ISO-abbreviation] Anticancer Res.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Greece
  • [Chemical-registry-number] 0 / Morphine Derivatives; 0 / P-Glycoprotein; 467-13-0 / 6-codeinone; Q830PW7520 / Codeine
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3. Atsumi T, Iwakura I, Fujisawa S, Ueha T: Reactive oxygen species generation and photo-cytotoxicity of eugenol in solutions of various pH. Biomaterials; 2001 Jun;22(12):1459-66
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  • In order to clarify the mechanism of photo-damage caused by eugenol (4-allyl-2-methoxyphenol), we measured cell survival in the presence of eugenol at concentrations of 10(-3) - 10(-7) M, with and without VL (visible light) irradiation by a VL dental lamp and at various pHs (7.2, 7.8 and 8.2) using two different cells (HSG, a human submandibular gland tumor cell line; HGF, a human gingival fibroblast in primary culture).
  • Cytotoxicity and ROS generation of HGF cells were significantly lower than that of HSG cells.
  • [MeSH-major] Cell Survival / drug effects. Eugenol / chemistry. Eugenol / toxicity. Fibroblasts / cytology. Gingiva / cytology. Hydrogen-Ion Concentration. Reactive Oxygen Species
  • [MeSH-minor] Carcinoma, Squamous Cell. Cell Adhesion. Cells, Cultured. Dental Restoration, Temporary. Dose-Response Relationship, Drug. Humans. Kinetics. Light. Photochemistry. Solutions. Submandibular Gland Neoplasms. Tumor Cells, Cultured

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  • (PMID = 11374444.001).
  • [ISSN] 0142-9612
  • [Journal-full-title] Biomaterials
  • [ISO-abbreviation] Biomaterials
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Reactive Oxygen Species; 0 / Solutions; 3T8H1794QW / Eugenol
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4. Tsurumaru D, Kuroiwa T, Yabuuchi H, Hirata H, Higaki Y, Tomita K: Efficacy of intra-arterial infusion chemotherapy for head and neck cancers using coaxial catheter technique: initial experience. Cardiovasc Intervent Radiol; 2007 Mar-Apr;30(2):207-11
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  • Thirty-one patients (21 males and 10 females; 37-83 years of age) with squamous cell carcinoma of the head and neck (maxilla, 2; epipharynx, 4; mesopharynx, 8; oral floor, 4; tongue, 10; lower gingiva, 1; buccal mucosa, 2) were treated by intra-arterial infusion chemotherapy.
  • The anticancer agent carboplatin (CBDCA) was continuously injected for 24 h through the microcatheter from a portable infusion pump attached to the patient's waist.
  • [MeSH-major] Antineoplastic Agents / therapeutic use. Carboplatin / therapeutic use. Carcinoma, Squamous Cell / drug therapy. Catheterization, Peripheral / methods. Head and Neck Neoplasms / drug therapy. Infusions, Intra-Arterial
  • [MeSH-minor] Adult. Aged. Aged, 80 and over. Area Under Curve. Brachytherapy. Female. Humans. Male. Middle Aged. Radiotherapy, Adjuvant. Temporal Arteries. Treatment Outcome. Tumor Burden / drug effects. Tumor Burden / radiation effects

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  • (PMID = 17216381.001).
  • [ISSN] 0174-1551
  • [Journal-full-title] Cardiovascular and interventional radiology
  • [ISO-abbreviation] Cardiovasc Intervent Radiol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antineoplastic Agents; BG3F62OND5 / Carboplatin
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5. Jiang Y, Kusama K, Satoh K, Takayama E, Watanabe S, Sakagami H: Induction of cytotoxicity by chlorogenic acid in human oral tumor cell lines. Phytomedicine; 2000 Dec;7(6):483-91
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  • Millimolar concentrations of chlorogenic acid (CGA) showed higher cytotoxic activity against human oral squamous cell carcinoma (HSC-2) and salivary gland tumor (HSG) cell lines, as compared with that against human gingival fibroblast (HGF).
  • ESR spectroscopy showed that higher (millimolar) concentrations of CGA produced radicals under alkaline conditions, acting as a prooxidant, whereas lower concentrations of CGA scavenged superoxide and hydroxyl radical.
  • Activation of caspase was demonstrated by staining with M30 monoclonal antibody, which reacts with degradation products of cytokeratin 18.
  • [MeSH-major] Anticarcinogenic Agents / toxicity. Carcinoma, Squamous Cell. Chlorogenic Acid / toxicity. Mouth Neoplasms
  • [MeSH-minor] DNA Fragmentation / drug effects. Dose-Response Relationship, Drug. Fibroblasts / drug effects. Gingiva / cytology. Humans. Salivary Gland Neoplasms. Tumor Cells, Cultured / drug effects

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  • (PMID = 11194177.001).
  • [ISSN] 0944-7113
  • [Journal-full-title] Phytomedicine : international journal of phytotherapy and phytopharmacology
  • [ISO-abbreviation] Phytomedicine
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Anticarcinogenic Agents; 318ADP12RI / Chlorogenic Acid
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6. Shirataki Y, Kawase M, Saito S, Kurihara T, Tanaka W, Satoh K, Sakagami H, Motohashi N: Selective cytotoxic activity of grape peel and seed extracts against oral tumor cell lines. Anticancer Res; 2000 Jan-Feb;20(1A):423-6
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  • Methanol and 70% methanol extracts of grape seed selectively killed two human oral tumor cell lines, more efficiently than human gingival fibroblasts.
  • On the other hand, lower concentration of these extracts slightly reduced the radical intensity of sodium ascorbate, and scavenged superoxide anion, generated by hypoxanthine and xanthine oxidase reaction.
  • [MeSH-major] Anticarcinogenic Agents / pharmacology. Antineoplastic Agents, Phytogenic / pharmacology. Carcinoma, Squamous Cell / pathology. Mouth Neoplasms / pathology. Plant Extracts / pharmacology. Rosales / chemistry
  • [MeSH-minor] Ascorbic Acid / pharmacology. Electron Spin Resonance Spectroscopy. Fibroblasts / drug effects. Free Radical Scavengers / pharmacology. Free Radicals. Gingiva / cytology. Humans. Hydrogen-Ion Concentration. Methanol. Oxidation-Reduction. Oxidative Stress. Seeds / chemistry. Solvents. Superoxides / metabolism. Tumor Cells, Cultured / drug effects

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  • (PMID = 10769690.001).
  • [ISSN] 0250-7005
  • [Journal-full-title] Anticancer research
  • [ISO-abbreviation] Anticancer Res.
  • [Language] eng
  • [Publication-type] Comparative Study; Journal Article
  • [Publication-country] GREECE
  • [Chemical-registry-number] 0 / Anticarcinogenic Agents; 0 / Antineoplastic Agents, Phytogenic; 0 / Free Radical Scavengers; 0 / Free Radicals; 0 / Plant Extracts; 0 / Solvents; 11062-77-4 / Superoxides; PQ6CK8PD0R / Ascorbic Acid; Y4S76JWI15 / Methanol
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7. Atsumi T, Fujisawa S, Tonosaki K: Relationship between intracellular ROS production and membrane mobility in curcumin- and tetrahydrocurcumin-treated human gingival fibroblasts and human submandibular gland carcinoma cells. Oral Dis; 2005 Jul;11(4):236-42
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  • [Title] Relationship between intracellular ROS production and membrane mobility in curcumin- and tetrahydrocurcumin-treated human gingival fibroblasts and human submandibular gland carcinoma cells.
  • OBJECTIVE: Curcumin is a well-known chemopreventive agent of oral cancers as well as stomach and intestinal cancers.
  • METHODS: The intracellular ROS production and membrane mobility by curcumin or TH-curcumin were measured in human submandibular adenocarcinoma cells (HSGs) and human primary gingival fibroblasts (HGFs).
  • The membrane mobility coefficient of the curcumin-treated cells was significantly lower than that of control cells.
  • [MeSH-major] Adenocarcinoma / metabolism. Curcumin / analogs & derivatives. Curcumin / pharmacology. Membrane Fluidity / drug effects. Oxidants / pharmacology. Reactive Oxygen Species / metabolism. Submandibular Gland Neoplasms / metabolism
  • [MeSH-minor] Anticarcinogenic Agents / chemistry. Anticarcinogenic Agents / pharmacology. Antioxidants / pharmacology. Cell Line, Tumor. Cells, Cultured. Dose-Response Relationship, Drug. Fibroblasts / metabolism. Fluorescence Recovery After Photobleaching. Gingiva / cytology. Gingiva / metabolism. Humans. Molecular Structure

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  • (PMID = 15984955.001).
  • [ISSN] 1354-523X
  • [Journal-full-title] Oral diseases
  • [ISO-abbreviation] Oral Dis
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Denmark
  • [Chemical-registry-number] 0 / Anticarcinogenic Agents; 0 / Antioxidants; 0 / Oxidants; 0 / Reactive Oxygen Species; 00U0645U03 / tetrahydrocurcumin; IT942ZTH98 / Curcumin
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8. Atsumi T, Tonosaki K, Fujisawa S: Induction of early apoptosis and ROS-generation activity in human gingival fibroblasts (HGF) and human submandibular gland carcinoma (HSG) cells treated with curcumin. Arch Oral Biol; 2006 Oct;51(10):913-21
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Induction of early apoptosis and ROS-generation activity in human gingival fibroblasts (HGF) and human submandibular gland carcinoma (HSG) cells treated with curcumin.
  • Loss of DeltaPsi(m), PS externalization and ROS generation were significantly more pronounced in HGF cells than in HSG cells at curcumin concentrations lower than about 15microM, and were inhibited by the addition of the antioxidants N-acetyl-l-cysteine and glutathione.
  • [MeSH-major] Apoptosis / drug effects. Curcumin / pharmacology. Gingiva / drug effects. Reactive Oxygen Species / metabolism. Submandibular Gland Neoplasms / pathology
  • [MeSH-minor] Antineoplastic Agents / pharmacology. Cell Survival / drug effects. Cells, Cultured. Child. Dose-Response Relationship, Drug. Female. Fibroblasts / drug effects. Fibroblasts / metabolism. Humans. Membrane Potential, Mitochondrial / drug effects. Phosphatidylserines / metabolism. Tumor Cells, Cultured


9. Ishibashi M, Masuda N, Noguchi K, Moridera K, Nishimura N, Takayama T, Nishioji K, Urade M, Kogo M: [Severe advanced lower gingival carcinoma effectively reduced by chemoradiation with S-1--report of a case]. Gan To Kagaku Ryoho; 2007 Nov;34(11):1837-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Severe advanced lower gingival carcinoma effectively reduced by chemoradiation with S-1--report of a case].
  • Severe advanced head and neck carcinoma which can not be removed via surgical procedure combined with a large lymph node metastasis has a poor prognosis.
  • We administered concurrent chemoradiotherapy with S-1 for a lower gingival carcinoma.
  • [MeSH-major] Antimetabolites, Antineoplastic / administration & dosage. Carcinoma, Squamous Cell / drug therapy. Carcinoma, Squamous Cell / radiotherapy. Gingival Neoplasms / drug therapy. Gingival Neoplasms / radiotherapy. Oxonic Acid / administration & dosage. Tegafur / administration & dosage
  • [MeSH-minor] Combined Modality Therapy. Drug Administration Schedule. Drug Combinations. Humans. Male. Middle Aged. Quality of Life. Radiotherapy Dosage

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  • (PMID = 18030019.001).
  • [ISSN] 0385-0684
  • [Journal-full-title] Gan to kagaku ryoho. Cancer & chemotherapy
  • [ISO-abbreviation] Gan To Kagaku Ryoho
  • [Language] jpn
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Japan
  • [Chemical-registry-number] 0 / Antimetabolites, Antineoplastic; 0 / Drug Combinations; 150863-82-4 / S 1 (combination); 1548R74NSZ / Tegafur; 5VT6420TIG / Oxonic Acid
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10. Momoi K, Sugita Y, Ishihara M, Satoh K, Kikuchi H, Hashimoto K, Yokoe I, Nishikawa H, Fujisawa S, Sakagami H: Cytotoxic activity of styrylchromones against human tumor cell lines. In Vivo; 2005 Jan-Feb;19(1):157-63
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  • A total of 6 newly-synthesized styrylchromones (SC-1 approximately SC-6) were compared for their cytotoxic activity against three normal oral human cells (gingival fibroblast HGF, pulp cell HPC, periodontal ligament fibroblast HPLF) and four human tumor cell lines (squamous cell carcinoma HSC-2, HSC-3, submandibular gland carcinoma HSG, promyelocytic leukemia HL-60).
  • The cytotoxic activity of SC-3 and SC-5 was slightly reduced by a lower concentration of NADH, a quinone reductase, but that of SC-3 was enhanced by higher concentrations of NADH, possibly due to demethylation of the methoxy groups.
  • [MeSH-major] Antineoplastic Agents / toxicity. Carcinoma, Squamous Cell / drug therapy. Chromones / chemistry. Chromones / toxicity. Mouth Neoplasms / drug therapy. Submandibular Gland Neoplasms / drug therapy
  • [MeSH-minor] Apoptosis / drug effects. Caspases / metabolism. Cell Line. Cell Line, Tumor. Dental Pulp / cytology. Dental Pulp / drug effects. Dental Pulp / metabolism. Drug Screening Assays, Antitumor. Electron Spin Resonance Spectroscopy. Electrophoresis, Agar Gel. Enzyme Activation / drug effects. Fibroblasts / drug effects. Fibroblasts / metabolism. Gingiva / cytology. HL-60 Cells. Humans. Periodontal Ligament / cytology. Structure-Activity Relationship

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  • (PMID = 15796168.001).
  • [ISSN] 0258-851X
  • [Journal-full-title] In vivo (Athens, Greece)
  • [ISO-abbreviation] In Vivo
  • [Language] eng
  • [Publication-type] Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Greece
  • [Chemical-registry-number] 0 / Antineoplastic Agents; 0 / Chromones; EC 3.4.22.- / Caspases
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11. Nakashiro K, Shintani S, Yano J, Shinohara Y, Terakado N, Hamakawa H: [A case of mandibular gingival cancer (T4) responding to concurrent chemoradiotherapy with TS-1]. Gan To Kagaku Ryoho; 2003 Sep;30(9):1309-12
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  • [Title] [A case of mandibular gingival cancer (T4) responding to concurrent chemoradiotherapy with TS-1].
  • The patient was an 82-year-old male who had a 41 x 22 mm tumor mass around the left lower gingiva, whose X-ray showed a bone resorption image reaching the mandibular canal.
  • [MeSH-major] Antimetabolites, Antineoplastic / therapeutic use. Carcinoma, Squamous Cell / drug therapy. Carcinoma, Squamous Cell / radiotherapy. Gingival Neoplasms / drug therapy. Gingival Neoplasms / radiotherapy. Oxonic Acid / therapeutic use. Pyridines / therapeutic use. Tegafur / therapeutic use
  • [MeSH-minor] Aged. Aged, 80 and over. Drug Administration Schedule. Drug Combinations. Humans. Male. Mandible. Radiotherapy Dosage

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  • (PMID = 14518411.001).
  • [ISSN] 0385-0684
  • [Journal-full-title] Gan to kagaku ryoho. Cancer & chemotherapy
  • [ISO-abbreviation] Gan To Kagaku Ryoho
  • [Language] jpn
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Japan
  • [Chemical-registry-number] 0 / Antimetabolites, Antineoplastic; 0 / Drug Combinations; 0 / Pyridines; 150863-82-4 / S 1 (combination); 1548R74NSZ / Tegafur; 5VT6420TIG / Oxonic Acid
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12. Okayasu H, Ishihara M, Satoh K, Sakagami H: Cytotoxic activity of vitamins K1, K2 and K3 against human oral tumor cell lines. Anticancer Res; 2001 Jul-Aug;21(4A):2387-92
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  • Among these compounds, vitamin K3 showed the highest cytotoxic activity against human oral tumor cell lines (HSC-2, HSG), human promyelocytic leukemic cell line (HL-60) and human gingival fibroblast (HGF).
  • The cytotoxic activity of vitamins K2 and K1 was one and two orders lower, respectively, than K3.
  • [MeSH-major] Mouth Neoplasms / drug therapy. Vitamin K / toxicity
  • [MeSH-minor] Carcinoma, Squamous Cell / drug therapy. DNA Fragmentation / drug effects. Electron Spin Resonance Spectroscopy. Fibroblasts / cytology. Fibroblasts / drug effects. Free Radical Scavengers / toxicity. Gingiva / cytology. Gingiva / drug effects. HL-60 Cells / drug effects. Humans. Models, Molecular. Salivary Gland Neoplasms / drug therapy. Structure-Activity Relationship. Superoxides / metabolism. Tumor Cells, Cultured. Vitamin K 1 / toxicity. Vitamin K 2 / toxicity. Vitamin K 3 / toxicity

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  • (PMID = 11724297.001).
  • [ISSN] 0250-7005
  • [Journal-full-title] Anticancer research
  • [ISO-abbreviation] Anticancer Res.
  • [Language] eng
  • [Publication-type] Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Greece
  • [Chemical-registry-number] 0 / Free Radical Scavengers; 11032-49-8 / Vitamin K 2; 11062-77-4 / Superoxides; 12001-79-5 / Vitamin K; 723JX6CXY5 / Vitamin K 3; 84-80-0 / Vitamin K 1
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13. Nakamura M, Nakatani K, Uzawa K, Ono K, Uesugi H, Ogawara K, Shiiba M, Bukawa H, Yokoe H, Wada T, Fujita S, Tanzawa H: Establishment and characterization of a cisplatin-resistant oral squamous cell carcinoma cell line, H-1R. Oncol Rep; 2005 Nov;14(5):1281-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Establishment and characterization of a cisplatin-resistant oral squamous cell carcinoma cell line, H-1R.
  • Cisplatin (CDDP) is a widely used potent chemotherapeutic agent for many malignancies.
  • To investigate the molecular mechanism, we established a CDDP-resistant cell line (H-1R) from a CDDP-sensitive cell line (H-1) which was derived from moderately differentiated squamous cell carcinoma of the lower gingiva.
  • [MeSH-major] Antineoplastic Agents / pharmacology. Carcinoma, Squamous Cell / pathology. Cisplatin / pharmacology. Mouth Neoplasms / pathology. Tumor Cells, Cultured
  • [MeSH-minor] ATP-Binding Cassette Transporters / biosynthesis. ATP-Binding Cassette Transporters / genetics. Drug Resistance, Neoplasm. Gene Expression Profiling. Humans. Male. Oligonucleotide Array Sequence Analysis


14. Nakatani K, Nakamura M, Uzawa K, Wada T, Seki N, Tanzawa H, Fujita S: Establishment and gene analysis of a cisplatin-resistant cell line, Sa-3R, derived from oral squamous cell carcinoma. Oncol Rep; 2005 Apr;13(4):709-14
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Establishment and gene analysis of a cisplatin-resistant cell line, Sa-3R, derived from oral squamous cell carcinoma.
  • Cisplatin (CDDP) is widely used for chemotherapy of many malignancies, especially of oral squamous cell carcinoma (SCC).
  • However, because the mechanism of resistance to CDDP is unclear, we established a CDDP-resistant cell line, Sa-3R, from a CDDP-sensitive cell line, Sa-3, which was derived from moderately differentiated SCC of the lower gingiva.
  • [MeSH-major] Carcinoma, Squamous Cell / genetics. Carcinoma, Squamous Cell / pathology. Cell Line, Tumor. Cisplatin / pharmacology. Drug Resistance, Neoplasm. Gene Expression Regulation, Neoplastic. Mouth Neoplasms / genetics. Mouth Neoplasms / pathology
  • [MeSH-minor] Biopsy. Cell Proliferation. Coloring Agents / pharmacology. DNA, Complementary / metabolism. Down-Regulation. Humans. Inhibitory Concentration 50. Male. Oligonucleotide Array Sequence Analysis. Phenotype. RNA, Messenger / metabolism. Reverse Transcriptase Polymerase Chain Reaction. Tetrazolium Salts / pharmacology. Thiazoles / pharmacology. Time Factors. Up-Regulation






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