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41. Ray M, Kindler HL: Malignant pleural mesothelioma: an update on biomarkers and treatment. Chest; 2009 Sep;136(3):888-896
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Malignant pleural mesothelioma: an update on biomarkers and treatment.
  • Although the insulating properties of asbestos have been known for millennia, the link between asbestos exposure and mesothelioma was not recognized until 1960, when it was first described in South African asbestos miners.
  • The incidence of mesothelioma parallels asbestos usage with a latency of 20 to 40+ years; thus, patient numbers are declining in the United States but rising in the developing world.
  • Newly described biomarkers, including soluble mesothelin-related peptide, megakaryocyte potentiation factor, and osteopontin, may predict which asbestos-exposed individuals will develop mesothelioma, and may prove useful in assessing response to treatment.
  • This combination improves response, survival, time to progression, pulmonary function, and disease-related symptoms.
  • As we learn more about mesothelioma biology, molecularly targeted agents may become treatment options.
  • [MeSH-major] Biomarkers, Tumor / analysis. Mesothelioma / therapy. Pleural Neoplasms / therapy


42. Gaafar R, Bahnassy A, Abdelsalam I, Kamel MM, Helal A, Abdel-Hamid A, Eldin NA, Mokhtar N: Tissue and serum EGFR as prognostic factors in malignant pleural mesothelioma. Lung Cancer; 2010 Oct;70(1):43-50
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  • [Title] Tissue and serum EGFR as prognostic factors in malignant pleural mesothelioma.
  • BACKGROUND: Malignant pleural mesothelioma (MPM) is an asbestos related aggressive tumor.
  • Asbestos causes genetic modifications and cell signaling events that favor resistance to chemotherapy.
  • [MeSH-major] Biomarkers, Tumor / biosynthesis. Mesothelioma / enzymology. Pleural Neoplasms / enzymology. Receptor, Epidermal Growth Factor / biosynthesis

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  • [Copyright] Copyright 2010 Elsevier Ireland Ltd. All rights reserved.
  • (PMID = 20347505.001).
  • [ISSN] 1872-8332
  • [Journal-full-title] Lung cancer (Amsterdam, Netherlands)
  • [ISO-abbreviation] Lung Cancer
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Ireland
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; EC 2.7.10.1 / Receptor, Epidermal Growth Factor
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43. Roe OD, Creaney J, Lundgren S, Larsson E, Sandeck H, Boffetta P, Nilsen TI, Robinson B, Kjaerheim K: Mesothelin-related predictive and prognostic factors in malignant mesothelioma: a nested case-control study. Lung Cancer; 2008 Aug;61(2):235-43
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  • [Title] Mesothelin-related predictive and prognostic factors in malignant mesothelioma: a nested case-control study.
  • Soluble mesothelin-related protein (SMRP) in serum is potentially a sensitive marker of malignant mesothelioma (MM) diagnosis and progression, and may be useful as screening marker.
  • Levels of SMRP, CA125 and CYFRA 21-1 in pre-diagnostic (1-30 years) serum samples from 47 mesothelioma cases and 141 matched controls were analysed.
  • The association between biomarker level and mesothelioma risk and survival was analysed, adjusting for asbestos exposure.
  • Survival related to tumor mesothelin expression, age, sex, histological type, location, asbestos exposure and pre-clinical SMRP was analysed.
  • There was no significant association between biomarker levels and mesothelioma risk when analysed as continuous variables or as tertiles.
  • Biomarker levels <10, 10-19 and >or=20 years before diagnosis were not significantly associated to mesothelioma risk.
  • Mesothelin expression in <50% of tumor cells was a significant negative prognostic marker in all cases of malignant mesothelioma (median survival=6 months vs. 12 months, hazard ratio (HR)=2.49, 95%CI 1.17-5.27), and also when only epithelial mesothelioma was analysed (median=6 months vs. 14 months, HR=2.36, 95%CI 1.07-5.22).
  • High age (>65 years) was an independent negative prognostic factor that was related to both mesothelin expression and asbestos exposure.
  • Mesothelioma of the epithelial type of the peritoneum had a significantly longer survival than epithelial type in pleura and was also related to mesothelin expression.
  • [MeSH-major] Antigens, Neoplasm / blood. Biomarkers, Tumor / blood. Keratins / blood. Membrane Glycoproteins / blood. Mesothelioma / diagnosis. Peritoneal Neoplasms / diagnosis. Pleural Neoplasms / diagnosis. Proteins / metabolism
  • [MeSH-minor] Adolescent. Adult. Age Factors. Asbestos / adverse effects. Case-Control Studies. Child. Child, Preschool. Female. GPI-Linked Proteins. Humans. Infant. Keratin-19. Male. Occupational Exposure / adverse effects. Prognosis. Survival Analysis

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  • (PMID = 18281122.001).
  • [ISSN] 0169-5002
  • [Journal-full-title] Lung cancer (Amsterdam, Netherlands)
  • [ISO-abbreviation] Lung Cancer
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Ireland
  • [Chemical-registry-number] 0 / Antigens, Neoplasm; 0 / Biomarkers, Tumor; 0 / GPI-Linked Proteins; 0 / Keratin-19; 0 / Membrane Glycoproteins; 0 / NBR1 protein, human; 0 / Proteins; 0 / antigen CYFRA21.1; 0 / mesothelin; 1332-21-4 / Asbestos; 68238-35-7 / Keratins
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4. Bolognesi C, Martini F, Tognon M, Filiberti R, Neri M, Perrone E, Landini E, Canessa PA, Ivaldi GP, Betta P, Mutti L, Puntoni R: A molecular epidemiology case control study on pleural malignant mesothelioma. Cancer Epidemiol Biomarkers Prev; 2005 Jul;14(7):1741-6
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  • [Title] A molecular epidemiology case control study on pleural malignant mesothelioma.
  • Pleural malignant mesothelioma is an uncommon neoplasm usually associated with asbestos exposure.
  • The increasing incidence of malignant mesothelioma cases involving individuals with low levels of asbestos exposure suggests a complex carcinogenetic process with the involvement of other cofactors.
  • A biomonitoring study was carried out to evaluate the micronuclei frequency in PBLs of patients with pleural malignant mesothelioma with respect to lung cancer, healthy, and risk controls as a marker of cancer susceptibility in correlation with the presence of SV40.
  • A significant increased micronuclei frequency was observed in patients with malignant mesothelioma in comparison with all the other groups, the mean micronuclei frequency was double in patients with malignant mesothelioma compared with healthy controls, risk controls, and patients with lung adenocarcinoma (median 11.4 binucleated cells with micronuclei/1,000 binucleated cells versus 6.2, 6.1, and 5.1, respectively).
  • Evidence of cytogenetic damage revealed as micronuclei frequency in mesothelioma cancer patients could be related to exogenous and endogenous cofactors besides asbestos exposure.
  • [MeSH-major] Asbestos / adverse effects. Lung Neoplasms / genetics. Mesothelioma / etiology. Molecular Epidemiology. Pleural Neoplasms / etiology. Smoking / adverse effects

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  • (PMID = 16030111.001).
  • [ISSN] 1055-9965
  • [Journal-full-title] Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology
  • [ISO-abbreviation] Cancer Epidemiol. Biomarkers Prev.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 1332-21-4 / Asbestos
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45. Park EK, Sandrini A, Yates DH, Creaney J, Robinson BW, Thomas PS, Johnson AR: Soluble mesothelin-related protein in an asbestos-exposed population: the dust diseases board cohort study. Am J Respir Crit Care Med; 2008 Oct 15;178(8):832-7
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  • [Title] Soluble mesothelin-related protein in an asbestos-exposed population: the dust diseases board cohort study.
  • RATIONALE: Soluble mesothelin-related protein (SMRP) is raised in epithelial-type malignant mesothelioma (MM), but the utility of SMRP in screening for MM is unknown.
  • OBJECTIVES: We aimed to evaluate SMRP in an asbestos-exposed cohort.
  • MEASUREMENTS AND MAIN RESULTS: Mean (+/-SD) SMRP in healthy subjects exposed to asbestos (n = 223) was 0.79 (+/-0.45) nM.
  • CONCLUSIONS: This is the first large-scale prospective study of SMRP for screening for malignancy in asbestos-exposed individuals.
  • [MeSH-major] Asbestos / adverse effects. Membrane Glycoproteins / biosynthesis. Mesothelioma / diagnosis. Occupational Diseases / diagnosis. Occupational Exposure / adverse effects. Pleural Neoplasms / diagnosis

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  • [CommentIn] Am J Respir Crit Care Med. 2008 Oct 15;178(8):781-2 [18832552.001]
  • [CommentIn] Am J Respir Crit Care Med. 2009 May 1;179(9):851; author reply 851-852 [19383930.001]
  • (PMID = 18583574.001).
  • [ISSN] 1535-4970
  • [Journal-full-title] American journal of respiratory and critical care medicine
  • [ISO-abbreviation] Am. J. Respir. Crit. Care Med.
  • [Language] eng
  • [Publication-type] Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / Blood Proteins; 0 / GPI-Linked Proteins; 0 / Membrane Glycoproteins; 0 / mesothelin; 1332-21-4 / Asbestos
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46. Martínez González C, Cruz Carmona MJ: [Update in respiratory disease and environmental exposure: an invisible relationship]. Arch Bronconeumol; 2009;45 Suppl 1:21-4
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  • In the case of neoplastic diseases associated with asbestos inhalation, the areas of most interest have been in the search for tumour markers, the importance of the determination of asbestos fibre deposits in biological samples, and new therapeutic schemes in malignant pleural mesothelioma.
  • A consensus article has been published on occupational asthma, in which some clinical evidenced-based recommendations are established, directed at the diagnosis and management of work-related asthma.

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  • (PMID = 19303526.001).
  • [ISSN] 0300-2896
  • [Journal-full-title] Archivos de bronconeumología
  • [ISO-abbreviation] Arch. Bronconeumol.
  • [Language] spa
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Spain
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47. McCoy MJ, Nowak AK, Lake RA: Chemoimmunotherapy: an emerging strategy for the treatment of malignant mesothelioma. Tissue Antigens; 2009 Jul;74(1):1-10
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  • [Title] Chemoimmunotherapy: an emerging strategy for the treatment of malignant mesothelioma.
  • Whether the immune system can recognize malignant and premalignant cells and eliminate them to prevent the development of cancer is still a matter of open debate, but in our view, the balance of evidence favours this concept.
  • Malignant mesothelioma has traditionally been considered a relatively non-immunogenic cancer.
  • However, mesothelioma cells do express a set of well-defined tumour antigens that have been shown to engage with the host immune system.
  • Mesothelioma should therefore be considered a target for immunotherapy.
  • A variety of anticancer immunotherapies have been investigated in mesothelioma and in other malignancies, although these have been largely ineffective when used in isolation.
  • Here, we discuss the rationale behind combining these two, long considered antagonistic, treatment options in the context of malignant mesothelioma.
  • [MeSH-major] Antigens, Neoplasm / immunology. Antineoplastic Agents / therapeutic use. Immunosuppression. Mesothelioma / therapy. Neoplasms, Mesothelial / therapy


48. Harding AH, Darnton A, Wegerdt J, McElvenny D: Mortality among British asbestos workers undergoing regular medical examinations (1971-2005). Occup Environ Med; 2009 Jul;66(7):487-95
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  • [Title] Mortality among British asbestos workers undergoing regular medical examinations (1971-2005).
  • OBJECTIVES: The Great Britain Asbestos Survey was established to monitor mortality among workers covered by regulations to control occupational exposure to asbestos.
  • This study updates the estimated burden of asbestos-related mortality in the cohort, and identifies risk factors associated with mortality.
  • The SMR for all cause mortality was 141 (95% CI 139 to 143) and for all malignant neoplasms 163 (95% CI 159 to 167).
  • The SMRs for cancers of the stomach (166), lung (187), peritoneum (3730) and pleura (968), mesothelioma (513), cerebrovascular disease (164) and asbestosis (5594) were statistically significantly elevated, as were the corresponding PMRs.
  • In age and sex adjusted analysis, birth cohort, age at first exposure, year of first exposure, duration of exposure, latency and job type were associated with the relative risk of lung, pleural and peritoneal cancers, asbestosis and mesothelioma mortality.
  • CONCLUSIONS: Known associations between asbestos exposure and mortality from lung, peritoneal and pleural cancers, mesothelioma and asbestosis were confirmed, and evidence of associations with stroke and stomach cancer mortality was observed.
  • Limited evidence suggested that asbestos-related disease risk may be lower among those first exposed in more recent times.
  • [MeSH-major] Asbestos / toxicity. Neoplasms / mortality. Occupational Diseases / mortality. Occupational Exposure / adverse effects

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  • [CommentIn] Occup Environ Med. 2009 Dec;66(12):854-5 [19934119.001]
  • (PMID = 19254909.001).
  • [ISSN] 1470-7926
  • [Journal-full-title] Occupational and environmental medicine
  • [ISO-abbreviation] Occup Environ Med
  • [Language] eng
  • [Publication-type] Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't
  • [Publication-country] England
  • [Chemical-registry-number] 1332-21-4 / Asbestos
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49. Antonescu-Turcu AL, Schapira RM: Parenchymal and airway diseases caused by asbestos. Curr Opin Pulm Med; 2010 Mar;16(2):155-61
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  • [Title] Parenchymal and airway diseases caused by asbestos.
  • PURPOSE OF REVIEW: The extensive industrial use of asbestos for many decades has been linked to development of benign and malignant pleuropulmonary disease.
  • This review summarizes newer evidence and ongoing controversies that exist in the literature regarding asbestos-related parenchymal and airway diseases.
  • RECENT FINDINGS: Asbestosis represents a significant respiratory problem despite the improvement in the workplace hygiene and a decrease in use of asbestos.
  • The role of asbestos exposure alone as a cause of chronic airway obstruction remains uncertain.
  • The relationship between lung cancer and asbestos exposure alone and in combination with smoking has also been investigated.
  • The benefit of screening for asbestos-related pleuropulmonary disease remains uncertain as does the use of computed tomography scanning for the purpose of screening.
  • SUMMARY: Future studies will help clarify the clinical issues and shape screening strategies for asbestos-exposed individuals.
  • [MeSH-major] Asbestos / adverse effects. Asbestosis / etiology. Lung Diseases / chemically induced
  • [MeSH-minor] Humans. Lung Diseases, Obstructive / chemically induced. Lung Diseases, Obstructive / radiography. Lung Neoplasms / chemically induced. Lung Neoplasms / radiography. Mesothelioma / chemically induced. Mesothelioma / radiography. Tomography, X-Ray Computed

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  • (PMID = 20104177.001).
  • [ISSN] 1531-6971
  • [Journal-full-title] Current opinion in pulmonary medicine
  • [ISO-abbreviation] Curr Opin Pulm Med
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Chemical-registry-number] 1332-21-4 / Asbestos
  • [Number-of-references] 34
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50. Schneider J, Bernges U: CYP1A1 and CYP1B1 polymorphisms as modifying factors in patients with pneumoconiosis and occupationally related tumours: A pilot study. Mol Med Rep; 2009 Nov-Dec;2(6):1023-8
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  • [Title] CYP1A1 and CYP1B1 polymorphisms as modifying factors in patients with pneumoconiosis and occupationally related tumours: A pilot study.
  • The effect of CYP1A1 and CYP1B1 polymorphisms as genetic modifiers of risk was investigated in individuals with asbestos, silica dust or ionizing radiation-induced occupational tumours compared to exposed non-cancer subjects suffering from pneumoconiosis, particularly in relation to tobacco smoking.
  • CYP1A1 T6235C, CYP1A1 A4889G and CYP1B1 codon 432 polymorphisms were determined by real-time PCR analysis in patients with asbestos-related lung cancer (n=39), patients with diffuse malignant mesotheliomas (n=19), lung cancer in silicosis patients (n=7), uranium miners with lung cancer (UMLC) (n=40), patients with asbestosis (n=181), and silicosis patients (n=204).
  • The risk for patients with the susceptible CYP1A1 A4889G allele was calculated as being between OR=0.39 (95% CI 0.10-1.54) for mesothelioma patients and OR=1.54 (95% CI 0.49-4.89) for UMLC.
  • CYP1B1 Val432Leu polymorphisms were associated with a risk of OR=0.56 (95% CI 0.2-1.55) for UMLC and OR=1.52 (95% CI 0.68-3.39) for asbestos-exposed lung cancer patients.
  • In this pilot study, the analyzed polymorphism had no consistent modifying effect on pneumoconiosis or occupationally related tumours.

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  • (PMID = 21475938.001).
  • [ISSN] 1791-3004
  • [Journal-full-title] Molecular medicine reports
  • [ISO-abbreviation] Mol Med Rep
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Greece
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51. Gaafar RM, Eldin NH: Epidemic of mesothelioma in Egypt. Lung Cancer; 2005 Jul;49 Suppl 1:S17-20
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  • [Title] Epidemic of mesothelioma in Egypt.
  • Asbestos has been recognized in Egypt since a long time as ancient Egyptians were using it in mummification.
  • Mesothelioma in Egypt is mainly attributed to environmental origin with a high incidence of women and young adults affected.
  • The incidence of mesothelioma is rising in Egypt.
  • Epidemiological data for 635 malignant mesothelioma (MM) patients over 4 years in the third Millennium were collected from the National Cancer Institute (NCI), Cairo University and Abbassia Chest hospital.
  • A clinicopathological study was done for 100 malignant pleural mesothelioma (MPM) patients and showed that asbestos exposure and SV40 positivity were evident in 67% and 60% of cases, respectively.
  • Evaluation of p53 and pRb immunohistochemically showed that pRb alteration was related to poor survival.
  • Asbestos in Cairo is a silent killer and measures toward eliminating it entirely or at least strictly controlling human contact with this dangerous carcinogen have to be taken in order to combat the coming epidemic of mesothelioma in Egypt.
  • [MeSH-major] Asbestos / adverse effects. Disease Outbreaks. Mesothelioma / epidemiology. Pleural Neoplasms / epidemiology


52. Putzu MG, Bruno C, Zona A, Massiccio M, Pasetto R, Piolatto PG, Comba P: Fluoro-edenitic fibres in the sputum of subjects from Biancavilla (Sicily): a pilot study. Environ Health; 2006;5:20
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  • BACKGROUND: An excess of mortality for malignant neoplasms of the pleura in Biancavilla, promoted an investigation for pleural mesothelioma, disclosing 17 cases.
  • As the absence of known sources of asbestos exposure, a local stone quarry, located near the inhabited area, used for the extraction of building materials, was investigated.
  • METHODS: Hypothesizing a behaviour of the new fibre analogous to that of asbestos, the determination of the free fibres and the ferruginous bodies in spontaneous sputum was carried out.
  • RESULTS: The preliminary findings are related to 12 subjects (7 females and 5 males).
  • CONCLUSION: The occurrence of the pleural mesothelioma cases and the presence of fluoro-edenitic fibres in spontaneous sputum, evidence the need to study the biological activity of fluoro-edenitic fibres and the implementation of epidemiological monitoring systems.
  • [MeSH-major] Environmental Exposure. Mesothelioma / etiology. Mineral Fibers / adverse effects. Mineral Fibers / analysis. Pleural Neoplasms / etiology
  • [MeSH-minor] Asbestos, Amphibole / adverse effects. Asbestos, Amphibole / analysis. Female. Fluorine. Geological Phenomena. Geology. Humans. Italy. Male. Middle Aged. Sputum / chemistry

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  • (PMID = 16780574.001).
  • [ISSN] 1476-069X
  • [Journal-full-title] Environmental health : a global access science source
  • [ISO-abbreviation] Environ Health
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Asbestos, Amphibole; 0 / Mineral Fibers; 284SYP0193 / Fluorine
  • [Other-IDs] NLM/ PMC1557492
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53. Kricka O, Matanić Lender D, Barković I, Flego V, Kupanovac Z, Bulat Kardum L: [Malignant pleural mesothelioma in patients hospitalised at the Clinical Hospital Centre Rijeka between 1989 and 2008]. Arh Hig Rada Toksikol; 2009 Nov;60 Suppl:41-3
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  • [Title] [Malignant pleural mesothelioma in patients hospitalised at the Clinical Hospital Centre Rijeka between 1989 and 2008].
  • Malignant pleural mesothelioma (MPM) is a relatively rare tumour, mainly associated with occupational exposure to asbestos.
  • Occupational exposure to asbestos was established in 72 patients who worked in shipbuilding.
  • We believe that this is not related to improved diagnostics, but to the long latency of the disease.
  • In the U.S.A. and Europe, MPM incidence is expected to peak by 2020, while in countries with poor control over asbestos use this may take longer.
  • [MeSH-major] Asbestos / adverse effects. Mesothelioma / epidemiology. Occupational Diseases / epidemiology. Pleural Neoplasms / epidemiology


54. Hollevoet K, Nackaerts K, Thimpont J, Germonpré P, Bosquée L, De Vuyst P, Legrand C, Kellen E, Kishi Y, Delanghe JR, van Meerbeeck JP: Diagnostic performance of soluble mesothelin and megakaryocyte potentiating factor in mesothelioma. Am J Respir Crit Care Med; 2010 Mar 15;181(6):620-5
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  • [Title] Diagnostic performance of soluble mesothelin and megakaryocyte potentiating factor in mesothelioma.
  • RATIONALE: Soluble mesothelin (SM) is currently the reference serum biomarker of malignant pleural mesothelioma (MPM).
  • METHODS: A total of 507 participants were enrolled in six cohorts: healthy control subjects (n = 101), healthy asbestos-exposed individuals (n = 89), and patients with benign asbestos-related disease (n = 123), benign respiratory disease (n = 46), lung cancer (n = 63), and MPM (n = 85).
  • [MeSH-major] Biomarkers, Tumor / blood. Membrane Glycoproteins / blood. Mesothelioma / blood. Mesothelioma / diagnosis. Pleural Neoplasms / blood

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  • (PMID = 20075387.001).
  • [ISSN] 1535-4970
  • [Journal-full-title] American journal of respiratory and critical care medicine
  • [ISO-abbreviation] Am. J. Respir. Crit. Care Med.
  • [Language] eng
  • [Publication-type] Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't; Validation Studies
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / GPI-Linked Proteins; 0 / Membrane Glycoproteins; 0 / mesothelin
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55. Aigner C, Hoda MA, Lang G, Taghavi S, Marta G, Klepetko W: Outcome after extrapleural pneumonectomy for malignant pleural mesothelioma. Eur J Cardiothorac Surg; 2008 Jul;34(1):204-7
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  • [Title] Outcome after extrapleural pneumonectomy for malignant pleural mesothelioma.
  • BACKGROUND: Malignant pleural mesothelioma is a mainly asbestos-related neoplasm that occurs with increasing frequency and is associated with a poor prognosis.
  • We therefore analysed our experience with extrapleural pneumonectomy in the treatment of malignant pleural mesothelioma.
  • METHODS: We retrospectively reviewed our institutional experience with all consecutive patients undergoing extrapleural pneumonectomy for malignant pleural mesothelioma from 1994 to 2005.
  • CONCLUSION: Extrapleural pneumonectomy as part of a multi-modality treatment regimen is a good treatment option for selected patients with malignant pleural mesothelioma.
  • [MeSH-major] Mesothelioma / surgery. Pleural Neoplasms / surgery. Pneumonectomy / methods

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  • (PMID = 18407510.001).
  • [ISSN] 1010-7940
  • [Journal-full-title] European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery
  • [ISO-abbreviation] Eur J Cardiothorac Surg
  • [Language] eng
  • [Publication-type] Evaluation Studies; Journal Article
  • [Publication-country] Germany
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56. Edakuni N, Ikuta K, Yano S, Nakataki E, Muguruma H, Uehara H, Tani M, Yokota J, Aizawa H, Sone S: Restored expression of the MYO18B gene suppresses orthotopic growth and the production of bloody pleural effusion by human malignant pleural mesothelioma cells in SCID mice. Oncol Res; 2006;16(5):235-43
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  • [Title] Restored expression of the MYO18B gene suppresses orthotopic growth and the production of bloody pleural effusion by human malignant pleural mesothelioma cells in SCID mice.
  • Malignant pleural mesothelioma (MPM) is closely related to exposure to asbestos, and a rapid increase in the number of MPM patients is therefore estimated to occur from 2010 to 2040 in Japan.
  • The inactivation of the MYO18B gene plays an important role in several malignant diseases.
  • [MeSH-major] Gene Expression Regulation, Neoplastic / genetics. Lung Neoplasms / genetics. Mesothelioma / genetics. Myosins / genetics. Myosins / pharmacology. Pleural Effusion / genetics. Pleural Neoplasms / genetics. Tumor Suppressor Proteins / genetics. Tumor Suppressor Proteins / pharmacology

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  • (PMID = 17294804.001).
  • [ISSN] 0965-0407
  • [Journal-full-title] Oncology research
  • [ISO-abbreviation] Oncol. Res.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / MYO18B protein, human; 0 / Tumor Suppressor Proteins; EC 3.6.4.1 / Myosins
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57. Heyer CM, Theile A, Weisser H, Reichert J, Horch C, Mueller KM, Bauer TT: Subarachnoid-pleural fistula as a complication of malignant pleural mesothelioma. Respirology; 2006 Jul;11(4):502-5
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  • [Title] Subarachnoid-pleural fistula as a complication of malignant pleural mesothelioma.
  • We report a 62-year-old male patient with asbestos-related malignant pleural mesothelioma who developed recurrent pleural effusions after surgical resection of paravertebral tumour masses.
  • Cytological studies of the pleural fluid showed no evidence of inflammatory or malignant cells.
  • A subarachnoid-pleural fistula has to be included in the differential diagnosis of patients with recurrent pleural effusions after surgical debulkment of malignant pleural mesothelioma.
  • [MeSH-major] Fistula / complications. Mesothelioma / pathology. Pleural Cavity / radiography. Pleural Neoplasms / pathology. Subarachnoid Space

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  • (PMID = 16771925.001).
  • [ISSN] 1323-7799
  • [Journal-full-title] Respirology (Carlton, Vic.)
  • [ISO-abbreviation] Respirology
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Australia
  • [Chemical-registry-number] 0 / Biomarkers; 0 / Lipocalins; EC 5.3.- / Intramolecular Oxidoreductases; EC 5.3.99.2 / prostaglandin R2 D-isomerase
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58. Rodríguez Portal JA, Rodríguez Becerra E, Rodríguez Rodríguez D, Alfageme Michavila I, Quero Martínez A, Diego Roza C, León Jiménez A, Isidro Montes I, Cebollero Rivas P: Serum levels of soluble mesothelin-related peptides in malignant and nonmalignant asbestos-related pleural disease: relation with past asbestos exposure. Cancer Epidemiol Biomarkers Prev; 2009 Feb;18(2):646-50
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  • [Title] Serum levels of soluble mesothelin-related peptides in malignant and nonmalignant asbestos-related pleural disease: relation with past asbestos exposure.
  • BACKGROUND: Malignant pleural mesothelioma (MPM) results from malignant transformation of mesothelial cells.
  • Past asbestos exposure represents a major risk factor for MPM and other benign pleural disease.
  • Soluble mesothelin-related peptides (SMRP) have been regarded as a promising serum biomarker for MPM.
  • The aim of this study was to investigate serum levels of SMRP in malignant and nonmalignant asbestos-related pleural disease.
  • PATIENTS: Four groups of patients were investigated: group 1 composed of 48 healthy subjects, group 2 composed of 177 patients with previous asbestos exposure and no pleural disease, group 3 composed of 36 patients with MPM, and group 4 composed of 101 patients with previous asbestos exposure and benign pleural disease.
  • Subjects exposed to asbestos had higher SMRP concentrations than normal control subjects regardless of the presence of pleural disease.
  • CONCLUSIONS: These data attest to good diagnostic sensitivity and specificity of SMRP for the diagnosis of malignant mesothelioma.
  • We have also shown that serum SMRP levels might serve as a marker of asbestos exposure.
  • [MeSH-major] Asbestosis / blood. Biomarkers, Tumor / blood. Membrane Glycoproteins / blood. Mesothelioma / blood. Pleural Neoplasms / blood

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  • (PMID = 19190155.001).
  • [ISSN] 1055-9965
  • [Journal-full-title] Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology
  • [ISO-abbreviation] Cancer Epidemiol. Biomarkers Prev.
  • [Language] eng
  • [Publication-type] Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / GPI-Linked Proteins; 0 / Membrane Glycoproteins; 0 / mesothelin
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59. Miles SE, Sandrini A, Johnson AR, Yates DH: Clinical consequences of asbestos-related diffuse pleural thickening: A review. J Occup Med Toxicol; 2008;3:20
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  • [Title] Clinical consequences of asbestos-related diffuse pleural thickening: A review.
  • Asbestos-related diffuse pleural thickening (DPT), or extensive fibrosis of the visceral pleura secondary to asbestos exposure, is increasingly common due to the large number of workers previously exposed to asbestos.
  • It may coexist with asbestos related pleural plaques but has a distinctly different pathology.
  • Generation of reactive oxygen and nitrogen species, profibrotic cytokines and growth factors in response to asbestos is likely to play a role in the formation of a fibrinous intrapleural matrix.
  • Benign asbestos related pleural effusions commonly antedate the development of diffuse pleural thickening.
  • Environmental as well as occupational exposure to asbestos may also result in pleural fibrosis, particularly in geographic areas with naturally occurring asbestiform soil minerals.
  • High resolution computed tomography (CT) is more sensitive and specific than chest radiography for the diagnosis of diffuse pleural thickening, and several classification systems for asbestos-related disorders have been devised.
  • Magnetic resonance imaging and fluorodeoxyglucose positron emission tomography (PET) scanning may be useful in distinguishing between DPT and malignant mesothelioma.

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  • (PMID = 18775081.001).
  • [ISSN] 1745-6673
  • [Journal-full-title] Journal of occupational medicine and toxicology (London, England)
  • [ISO-abbreviation] J Occup Med Toxicol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
  • [Other-IDs] NLM/ PMC2553409
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60. Proietti L, Spicuzza L, Di Maria A, Polosa R, Sebastian Torres E, Asero V, Di Maria GU: Non-occupational malignant pleural mesothelioma due to asbestos and non-asbestos fibres. Monaldi Arch Chest Dis; 2006 Dec;65(4):210-6
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  • [Title] Non-occupational malignant pleural mesothelioma due to asbestos and non-asbestos fibres.
  • BACKGROUND AND AIM: The occurrence of malignant pleural mesothelioma (MPM) has been reported among population groups with no documented professional exposure to asbestos fibres living in different geographic areas.
  • This paper reviews existing data related to non occupational MPM including its occurrence in the province of Catania (Sicily, Italy).
  • METHODS: An electronic search of literature related to non occupational MPM was performed including the year 2005.
  • RESULTS: Non occupational MPM in subjects living in areas contaminated by a variety of asbestos and non asbestos fibres has been well documented through a number of epidemiologic studies including cases series, case-control studies, and a cohort study.
  • CONCLUSION: It is likely that genetic predisposition and non-occupational exposure to low doses of asbestos and asbestos-like fibres may concur to the development of malignant mesothelioma.

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  • (PMID = 17393666.001).
  • [ISSN] 1122-0643
  • [Journal-full-title] Monaldi archives for chest disease = Archivio Monaldi per le malattie del torace
  • [ISO-abbreviation] Monaldi Arch Chest Dis
  • [Language] ENG
  • [Publication-type] Journal Article; Review
  • [Publication-country] Italy
  • [Chemical-registry-number] 0 / Carcinogens; 0 / Mineral Fibers; 1332-21-4 / Asbestos
  • [Number-of-references] 86
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61. Candura SM, Canto A, Amatu A, Gerardini M, Stella G, Mensi M, Poggi G: Malignant mesothelioma of the tunica vaginalis testis in a petrochemical worker exposed to asbestos. Anticancer Res; 2008 Mar-Apr;28(2B):1365-8
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  • [Title] Malignant mesothelioma of the tunica vaginalis testis in a petrochemical worker exposed to asbestos.
  • Malignant mesothelioma of the tunica vaginalis testis is a rare and aggressive asbestos-related malignancy that may pose difficult diagnostic problems.
  • After 16 years of asbestos exposure, a 38-year-old petrochemical worker came to our notice with acute right testicular pain and swelling, simulating torsion of the spermatic cord.
  • Immunohistochemical staining for the epithelial glycoprotein Ber-EP4 was negative, whereas results were positive for mesothelial markers, thus leading to the diagnosis of epithelial mesothelioma.
  • Tunical mesothelioma may simulate metastatic carcinoma at routine histopathological examination.
  • Immunohistochemistry and occupational anamnesis are helpful for the correct diagnosis, which, in turn, is important for prognosis and treatment, and in relation to legal issues when asbestos is involved in the causation of the disease.
  • [MeSH-major] Asbestos / poisoning. Chemical Industry. Mesothelioma / etiology. Occupational Diseases / etiology. Occupational Exposure / adverse effects. Testicular Neoplasms / etiology


62. Aceto N, Bertino P, Barbone D, Tassi G, Manzo L, Porta C, Mutti L, Gaudino G: Taurolidine and oxidative stress: a rationale for local treatment of mesothelioma. Eur Respir J; 2009 Dec;34(6):1399-407
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  • [Title] Taurolidine and oxidative stress: a rationale for local treatment of mesothelioma.
  • Malignant mesothelioma is an asbestos-related, aggressive tumour, resistant to most anticancer therapies.
  • Akt is a key mediator of mesothelioma cell survival and chemoresistance.
  • This study aimed to clarify the mechanism by which taurolidine (TN), a known synthetic compound with antimicrobial and antineoplastic properties, leads to mesothelioma cell death.
  • TN induces cell death of mesothelioma cells, but not of non-neoplastic human mesothelial cells.
  • After TN treatment of mesothelioma cells, Akt but not extracellular signal-regulated kinase (Erk) 1/2 activity is inhibited a in time- and dose-dependent manner.
  • TN induces mesothelioma cell death via oxidative stress, accompanied by inhibition of Akt signalling.
  • This provides a promising molecular rationale for TN as local treatment of malignant mesothelioma.
  • [MeSH-major] Antineoplastic Agents / therapeutic use. Lung Neoplasms / drug therapy. Lung Neoplasms / pathology. Mesothelioma / drug therapy. Mesothelioma / pathology. Oxidative Stress. Taurine / analogs & derivatives. Thiadiazines / therapeutic use


63. Ascoli V, Cavone D, Merler E, Barbieri PG, Romeo L, Nardi F, Musti M: Mesothelioma in blood related subjects: report of 11 clusters among 1954 Italy cases and review of the literature. Am J Ind Med; 2007 May;50(5):357-69
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  • [Title] Mesothelioma in blood related subjects: report of 11 clusters among 1954 Italy cases and review of the literature.
  • BACKGROUND: Malignant mesothelioma is a sporadic tumor related to asbestos.
  • METHODS: The study analyses the features of mesothelioma in blood relatives that might explain the disease clustering.
  • Data sources of familial clusters were three population-based Mesothelioma Registries in Italy (Veneto and Apulia Regions, Brescia province; 1978-2005) and Medline, Toxline, and Oshline/Hseline databases for a review of the literature (1968-2006).
  • RESULTS: Eleven clusters (22 cases) were identified among 1954 Italy mesothelioma cases, and 51 clusters (120 cases) were extracted from 33 studies.
  • The proportion of Italy familial cases was 1.4 per 100 mesothelioma cases; the ratio between the number of familial clusters and the number of non-familial mesothelioma cases was 1:148.
  • The mesothelioma profile in consanguineous is the same as in non-consanguineous subjects (male prevalence; pleural site; age at diagnosis >50 years; asbestos exposure).
  • Most clusters occurred in asbestos workers (shipyard, asbestos-cement production/processing, and insulation) and household-exposed blood relatives.
  • Others were related to asbestos-cement factory pollution, asbestos-in-place, and handling asbestos-contaminated textiles.
  • CONCLUSIONS: Available data support asbestos exposure as the main risk factor in mesothelioma cases among blood relatives.
  • Our finding of a low proportion of familial cases would not suggest the influence of a large genetic component for mesothelioma in blood relatives.
  • [MeSH-major] Asbestos / toxicity. Environmental Exposure / adverse effects. Mesothelioma / genetics. Occupational Exposure / adverse effects


64. Dainese E, Pozzi B, Milani M, Rossi G, Pezzotta MG, Vertemati G, Tricomi P, Sessa F: Primary pleural epithelioid angiosarcoma. A case report and review of the literature. Pathol Res Pract; 2010 Jun 15;206(6):415-9
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  • Malignant vascular tumors are uncommon sarcomas that arise from endothelial cells of small blood vessels and may affect every organ.
  • Even if etiological factors implicated in the development of vascular sarcomas are still unclear, the strongest association with the disease was a history of chronic tuberculous pyothorax, observed only in Japanese patients, while prior radiotherapy and occupational exposure to asbestos have been reported in few Western cases.
  • Histological features and clinical presentation often cause several problems in the differential diagnosis, particularly with mesothelioma and metastasis from poorly differentiated carcinomas.
  • Immunohistochemistry plays an important role in identifying these rare entities, confirming the endothelial origin of the neoplasm with the expression of at least one of the vascular markers CD31, CD34, or factor VIII-related antigen.
  • [MeSH-minor] Biomarkers, Tumor / analysis. Diabetes Mellitus, Type 2. Diagnosis, Differential. Female. Humans. Immunohistochemistry. Male. Mesothelioma / pathology. Middle Aged. Neoplasm Metastasis / pathology. Radiculopathy / complications

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  • [Copyright] 2009 Elsevier GmbH. All rights reserved.
  • (PMID = 20089367.001).
  • [ISSN] 1618-0631
  • [Journal-full-title] Pathology, research and practice
  • [ISO-abbreviation] Pathol. Res. Pract.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Biomarkers, Tumor
  • [Number-of-references] 53
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65. De Bruin ML, Burgers JA, Baas P, van 't Veer MB, Noordijk EM, Louwman MW, Zijlstra JM, van den Berg H, Aleman BM, van Leeuwen FE: Malignant mesothelioma after radiation treatment for Hodgkin lymphoma. Blood; 2009 Apr 16;113(16):3679-81
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  • [Title] Malignant mesothelioma after radiation treatment for Hodgkin lymphoma.
  • Malignant mesothelioma is a relatively uncommon malignancy.
  • Although the pathogenesis is primarily related to asbestos, the disease may be associated with radiation exposure.
  • Recently, increased risks for second primary mesothelioma after radiation for lymphoma have been reported.
  • We examined mesothelioma risk in 2567 5-year survivors of Hodgkin lymphoma.
  • Although histology and survival of the mesothelioma cases were comparable with cases from the general population, asbestos exposure and the proportion of males were lower than expected.
  • The evidence for radiotherapy as cause for mesothelioma independent of exposure to asbestos is expanding, and the diagnosis of mesothelioma should be kept in mind whenever related symptoms arise in patients who had previous irradiation.
  • [MeSH-major] Hodgkin Disease / mortality. Hodgkin Disease / radiotherapy. Mesothelioma / mortality. Neoplasms, Radiation-Induced / mortality


66. Toyooka S, Kishimoto T, Date H: Advances in the molecular biology of malignant mesothelioma. Acta Med Okayama; 2008 Feb;62(1):1-7
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  • [Title] Advances in the molecular biology of malignant mesothelioma.
  • Malignant mesothelioma (MM) is a highly aggressive tumor with a dismal prognosis.
  • The incidence of MM is increasing as a result of widespread exposure to asbestos.
  • As in other malignant tumors, genes that are related to immortalization, proliferation, metastasis, angiogenesis, and anti-apoptosis are also overexpressed in MM, contributing to its malignant phenotype.
  • Although the causative role of asbestos is well-known in MM, much less information is available for MM than for other malignant tumors regarding the molecular alterations that occur in the disease.
  • [MeSH-major] Gene Expression Regulation, Neoplastic. Mesothelioma / genetics. Neoplasms, Glandular and Epithelial / genetics. Pleural Neoplasms / genetics


67. Nakataki E, Yano S, Matsumori Y, Goto H, Kakiuchi S, Muguruma H, Bando Y, Uehara H, Hamada H, Kito K, Yokoyama A, Sone S: Novel orthotopic implantation model of human malignant pleural mesothelioma (EHMES-10 cells) highly expressing vascular endothelial growth factor and its receptor. Cancer Sci; 2006 Mar;97(3):183-91
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  • [Title] Novel orthotopic implantation model of human malignant pleural mesothelioma (EHMES-10 cells) highly expressing vascular endothelial growth factor and its receptor.
  • Malignant pleural mesothelioma (MPM) is closely related to exposure to asbestos, and a rapid increase in the number of MPM patients in Japan is estimated in the years 2010-2050.
  • EHMES-10 cells overexpressed vascular endothelial growth factor (VEGF), a molecule responsible for malignant effusions, and its receptor.
  • [MeSH-major] Disease Models, Animal. Mesothelioma / metabolism. Pleural Neoplasms / metabolism. Receptors, Vascular Endothelial Growth Factor / biosynthesis. Vascular Endothelial Growth Factor A / biosynthesis


68. Musk AW, de Klerk NH, Reid A, Ambrosini GL, Fritschi L, Olsen NJ, Merler E, Hobbs MS, Berry G: Mortality of former crocidolite (blue asbestos) miners and millers at Wittenoom. Occup Environ Med; 2008 Aug;65(8):541-3
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  • [Title] Mortality of former crocidolite (blue asbestos) miners and millers at Wittenoom.
  • BACKGROUND: Blue asbestos was mined and milled at Wittenoom in Western Australia between 1943 and 1966.
  • Person-years at risk were derived using two censoring dates in order to produce minimum and maximum estimates of asbestos effect.
  • RESULTS: There have been 190 cases of pleural and 32 cases of peritoneal mesothelioma in this cohort of former workers at Wittenoom.
  • CONCLUSION: Asbestos related diseases, particularly malignant mesothelioma, lung cancer and pneumoconiosis, continue to be the main causes of excess mortality in the former blue asbestos miners and millers of Wittenoom.
  • [MeSH-major] Asbestos, Crocidolite / toxicity. Mesothelioma / mortality. Mining. Occupational Exposure / adverse effects. Peritoneal Neoplasms / mortality. Respiratory Tract Diseases / mortality

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  • (PMID = 18045848.001).
  • [ISSN] 1470-7926
  • [Journal-full-title] Occupational and environmental medicine
  • [ISO-abbreviation] Occup Environ Med
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] England
  • [Chemical-registry-number] 12001-28-4 / Asbestos, Crocidolite
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69. Di Serio F, Fontana A, Loizzi M, Capotorto G, Maggiolini P, Mera E, Bisceglia L, Molinini R: Mesothelin family proteins and diagnosis of mesothelioma: analytical evaluation of an automated immunoassay and preliminary clinical results. Clin Chem Lab Med; 2007;45(5):634-8
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  • [Title] Mesothelin family proteins and diagnosis of mesothelioma: analytical evaluation of an automated immunoassay and preliminary clinical results.
  • BACKGROUND: Studies have suggested that soluble mesothelin-related protein (SMRP) can be used as a serum marker of malignant mesothelioma.
  • The serum marker was analysed in 109 healthy subjects never exposed to asbestos, 26 healthy subjects exposed to asbestos, 33 patients with asbestosis, 33 with asbestos-related pleural plaques, 10 with non-malignant pleural diseases, 30 with lung cancer and 24 with histological diagnosis of pleural mesothelioma.
  • RESULTS: Using the International Mesothelioma Interest Group classification, there were nine stage IV, two stage III, four stage II and nine stage I patients.
  • Serum samples from patients with established pleural mesothelioma had significantly higher (p<0.05) concentrations of SMRP than control healthy and patient groups.
  • CONCLUSIONS: SMRP measured on automated systems could be useful for the diagnosis of mesothelioma in routine clinical practice.

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  • [CommentIn] Clin Chem Lab Med. 2008;46(4):565; author reply 566 [18298352.001]
  • (PMID = 17484626.001).
  • [ISSN] 1434-6621
  • [Journal-full-title] Clinical chemistry and laboratory medicine
  • [ISO-abbreviation] Clin. Chem. Lab. Med.
  • [Language] ENG
  • [Publication-type] Evaluation Studies; Journal Article
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / GPI-Linked Proteins; 0 / Membrane Glycoproteins; 0 / mesothelin
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70. Pesatori AC, Mensi C: Peculiar features of mesothelioma occurrence as related to exposure patterns and circumstances in the Lombard Region, Italy. Med Lav; 2005 Jul-Aug;96(4):354-9
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  • [Title] Peculiar features of mesothelioma occurrence as related to exposure patterns and circumstances in the Lombard Region, Italy.
  • BACKGROUND: The "Lombardy Mesothelioma Registry" started its activity in 2000 in accordance with Italian law DL 277/91.
  • OBJECTIVES AND METHODS: The Registry collects all new incident cases of Malignant Mesothelioma (MM) of pleura, peritoneum, pericardium and vaginal tunic of testis occurring in residents in the Lombardy Region (Northern Italy).
  • For confirmed cases, a standardized questionnaire is administered to the subject or next-of-kin, to verify sources of lifetime asbestos exposure.
  • 21 were peritoneal mesothelioma.
  • Standardized rates for pleural mesothelioma were respectively 3.7 and 1.4 per 100,000 for males and females.
  • Occupational asbestos exposure was ascertained for 71% of male cases and 26% of females.
  • The main relevant exposures were in building trades, metal manufacturing, machine production and maintenance; an unexpectedly high proportion of female cases was engaged in non-asbestos textile factories.
  • CONCLUSIONS: The high proportion of cases with unknown exposure underlines the need to explore new tools and sources to ascertain asbestos exposure.
  • An ad hoc survey in textile industries showed exposure to asbestos to be widely spread in this industry.
  • [MeSH-major] Mesothelioma / diagnosis. Occupational Diseases / diagnosis. Peritoneal Neoplasms / diagnosis. Pleural Neoplasms / diagnosis
  • [MeSH-minor] Adult. Aged. Asbestos / adverse effects. Carcinogens / toxicity. Female. Humans. Incidence. Italy / epidemiology. Male. Middle Aged. Occupational Exposure / adverse effects. Registries. Retrospective Studies. Surveys and Questionnaires

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  • (PMID = 16457432.001).
  • [ISSN] 0025-7818
  • [Journal-full-title] La Medicina del lavoro
  • [ISO-abbreviation] Med Lav
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Italy
  • [Chemical-registry-number] 0 / Carcinogens; 1332-21-4 / Asbestos
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71. Nishimura Y, Miura Y, Maeda M, Hayashi H, Dong M, Katsuyama H, Tomita M, Hyodoh F, Kusaka M, Uesaka A, Kuribayashi K, Fukuoka K, Nakano T, Kashimoto T, Osuki T: Expression of the T cell receptor Vbeta repertoire in a human T cell resistant to asbestos-induced apoptosis and peripheral blood T cells from patients with silica and asbestos-related diseases. Int J Immunopathol Pharmacol; 2006 Oct-Dec;19(4):795-805
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  • [Title] Expression of the T cell receptor Vbeta repertoire in a human T cell resistant to asbestos-induced apoptosis and peripheral blood T cells from patients with silica and asbestos-related diseases.
  • To explore the effects of asbestos and silica on the human immune system, an experimental model of low-dose and long-term exposure was established using a human HTLV-1-immortalized polyclonal T cell line, MT-2 (MT-2Org).
  • MT-2 cells were continuously exposed to asbestos at a concentration (10 microg/ml) which does not induce complete cell death during short-term exposure.
  • Patients with asbestos-related diseases (ARD), such as asbestosis and malignant mesothelioma, were compared with silicosis (SIL) patients as a disease control and with healthy donors (HD).
  • SIL and ARD not only differed in their causative materials, silica and asbestos as mineral silicates, but also in terms of complications; autoimmune disorders in SIL and tumors in ARD.
  • These experimental and clinical analyses indicate the superantigenic and dysregulation of autoimmunity-inducing effects of asbestos and silica, respectively.
  • [MeSH-major] Apoptosis / drug effects. Asbestos / toxicity. Asbestosis / immunology. Receptors, Antigen, T-Cell, alpha-beta / genetics. Silicon Dioxide / toxicity. Silicosis / immunology

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  • (PMID = 17166401.001).
  • [ISSN] 0394-6320
  • [Journal-full-title] International journal of immunopathology and pharmacology
  • [ISO-abbreviation] Int J Immunopathol Pharmacol
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Receptors, Antigen, T-Cell, alpha-beta; 1332-21-4 / Asbestos; 7631-86-9 / Silicon Dioxide
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72. Beyer HL, Geschwindt RD, Glover CL, Tran L, Hellstrom I, Hellstrom KE, Miller MC, Verch T, Allard WJ, Pass HI, Sardesai NY: MESOMARK: a potential test for malignant pleural mesothelioma. Clin Chem; 2007 Apr;53(4):666-72
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  • [Title] MESOMARK: a potential test for malignant pleural mesothelioma.
  • BACKGROUND: Soluble mesothelin-related peptides (SMRP)have been reported to be potential biomarkers for malignant pleural mesothelioma (MPM).
  • SMRP was increased in 52% and 5% of MPM patients and asbestos-exposed individuals, respectively.
  • Concentrations in other nonmalignant and malignant conditions were similar to those in healthy controls.
  • CONCLUSIONS: The MESOMARK assay is analytically robust and may be useful for the detection and management of mesothelioma.
  • [MeSH-major] Biomarkers, Tumor / blood. Membrane Glycoproteins / blood. Mesothelioma / diagnosis. Peptides / blood. Pleural Neoplasms / diagnosis

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  • (PMID = 17289801.001).
  • [ISSN] 0009-9147
  • [Journal-full-title] Clinical chemistry
  • [ISO-abbreviation] Clin. Chem.
  • [Language] eng
  • [Publication-type] Clinical Trial; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / GPI-Linked Proteins; 0 / Membrane Glycoproteins; 0 / Peptides; 0 / mesothelin
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73. Mirabelli D, Cavone D, Merler E, Gennaro V, Romanelli A, Mensi C, Chellini E, Nicita C, Marinaccio A, Magnani C, Musti M: Non-occupational exposure to asbestos and malignant mesothelioma in the Italian National Registry of Mesotheliomas. Occup Environ Med; 2010 Nov;67(11):792-4
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  • [Title] Non-occupational exposure to asbestos and malignant mesothelioma in the Italian National Registry of Mesotheliomas.
  • BACKGROUND: Malignant mesotheliomas are strictly related to asbestos, but in a proportion of cases no exposure can be recalled.
  • METHODS: To assess the role of non-occupational exposures in causing malignant mesotheliomas in Italy, the exposures of cases registered by the national mesothelioma registry (ReNaM) were examined.
  • RESULTS: From 1993 to 2001 ReNaM registered 5173 malignant mesothelioma cases, and exposures were assessed in 3552 of them.
  • 144 and 150 cases with exposures limited to environmental (living in the neighbourhood of an industrial or natural source of asbestos) or familial (living with a person occupationally exposed to asbestos) circumstances, respectively, were identified, accounting for 8.3% of all cases.
  • CONCLUSIONS: Geographical variations in the proportion of cases due to non-occupational exposures may be explained by the past distribution of asbestos-using industries.
  • [MeSH-major] Asbestos / toxicity. Environmental Exposure / adverse effects. Mesothelioma / etiology

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  • (PMID = 20959396.001).
  • [ISSN] 1470-7926
  • [Journal-full-title] Occupational and environmental medicine
  • [ISO-abbreviation] Occup Environ Med
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] England
  • [Chemical-registry-number] 1332-21-4 / Asbestos
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74. Tomasetti M, Amati M, Santarelli L, Alleva R, Neuzil J: Malignant mesothelioma: biology, diagnosis and therapeutic approaches. Curr Mol Pharmacol; 2009 Jun;2(2):190-206
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  • [Title] Malignant mesothelioma: biology, diagnosis and therapeutic approaches.
  • Malignant mesothelioma (MM) is an aggressive neoplasm of serosal cavities, which is resistant to conventional therapy, with patient survival from presentation of <12 months.
  • Although the main risk factor is asbestos exposure, other factors, Simian virus 40 infection and inheritance of susceptibility genes, likely play a role.
  • Asbestos-related carcinogenic process is primarily based on the interaction between susceptibility (genetic and acquired) and exposure to carcinogenic environmental agents.
  • Asbestos-induced carcinogenesis includes generation of reactive oxygen species, which induce DNA strand breaks and oxidant-induced base modifications to DNA.
  • Several programs have been used to screen asbestos-exposed individuals for lung and pleural disease.
  • [MeSH-major] Mesothelioma / diagnosis
  • [MeSH-minor] Asbestos / toxicity. Carcinogens / toxicity. DNA Damage. Humans. Mitogen-Activated Protein Kinases / metabolism. NF-kappa B / metabolism. Simian virus 40 / physiology. Transcription Factor AP-1 / metabolism

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  • (PMID = 20021458.001).
  • [ISSN] 1874-4702
  • [Journal-full-title] Current molecular pharmacology
  • [ISO-abbreviation] Curr Mol Pharmacol
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United Arab Emirates
  • [Chemical-registry-number] 0 / Carcinogens; 0 / NF-kappa B; 0 / Transcription Factor AP-1; 1332-21-4 / Asbestos; EC 2.7.11.24 / Mitogen-Activated Protein Kinases
  • [Number-of-references] 180
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75. Kurimoto R, Kishimoto T, Nagai Y, Takazawa H, Sakaue N, Shinohara Y, Hiroshima K: Malignant peritoneal mesothelioma: quantitative analysis of asbestos burden. Pathol Int; 2009 Nov;59(11):823-7
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  • [Title] Malignant peritoneal mesothelioma: quantitative analysis of asbestos burden.
  • Malignant mesotheliomas develop commonly in the pleural cavity and rarely arise in the peritoneal cavity.
  • It is well established that asbestos exposure is related to malignant pleural mesothelioma, but the asbestos burden in the abdominal cavity in patients with malignant peritoneal mesothelioma has not been well studied.
  • The purpose of the present study was therefore to report on an autopsy case of malignant peritoneal mesothelioma with quantitative analysis of the asbestos burden in tissues from the pleura and organs in the abdominal cavity.
  • The patient was a 67-year-old man with a history of asbestos exposure.
  • This patient was diagnosed as having malignant peritoneal epithelioid mesothelioma.
  • The number of asbestos fibers was >10,000/g dry tissue in all samples examined except in the small intestine.
  • The number of asbestos fibers in the stomach was 53,000/g, which was higher than that in a control asbestosis subject.
  • The existence of numerous asbestos fibers found in the abdominal cavity suggests that asbestos stimuli are related to the tumorigenesis of malignant peritoneal mesothelioma.
  • [MeSH-major] Asbestos / adverse effects. Asbestos / analysis. Asbestosis / pathology. Mesothelioma / etiology. Peritoneal Neoplasms / etiology

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  • (PMID = 19883435.001).
  • [ISSN] 1440-1827
  • [Journal-full-title] Pathology international
  • [ISO-abbreviation] Pathol. Int.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Australia
  • [Chemical-registry-number] 0 / Mineral Fibers; 1332-21-4 / Asbestos
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76. Hasegawa S: [Therapeutic strategies for resectable malignant pleural mesothelioma]. Nihon Geka Gakkai Zasshi; 2009 Nov;110(6):338-42
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  • [Title] [Therapeutic strategies for resectable malignant pleural mesothelioma].
  • Malignant pleural mesothelioma (MPM) is a rare thoracic malignancy associated with very poor prognosis.
  • The Mesothelioma and Radical Surgery (MARS) trial is a randomized clinical trial seeking to clarify the role of radical surgery in MPM treatment.
  • An all-Japan clinical study of trimodality treatment for MPM is currently underway as a part of a national campaign entitled "Comprehensive Strategy against Asbestos-Related Diseases. "
  • [MeSH-major] Mesothelioma / therapy. Pleural Neoplasms / therapy

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  • (PMID = 19999568.001).
  • [ISSN] 0301-4894
  • [Journal-full-title] Nihon Geka Gakkai zasshi
  • [ISO-abbreviation] Nihon Geka Gakkai Zasshi
  • [Language] jpn
  • [Publication-type] English Abstract; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Japan
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77. Catalano A, Lazzarini R, Di Nuzzo S, Orciari S, Procopio A: The plexin-A1 receptor activates vascular endothelial growth factor-receptor 2 and nuclear factor-kappaB to mediate survival and anchorage-independent growth of malignant mesothelioma cells. Cancer Res; 2009 Feb 15;69(4):1485-93
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  • [Title] The plexin-A1 receptor activates vascular endothelial growth factor-receptor 2 and nuclear factor-kappaB to mediate survival and anchorage-independent growth of malignant mesothelioma cells.
  • Here, we show that in asbestos-related malignant pleural mesothelioma (MPM), Semaphorin-6D (Sema6D) and its receptor plexin-A1 are frequently expressed and trigger a prosurvival program that promotes anchorage-independent growth of MPM cells.
  • Expression of Sema6D and plexin-A1 is induced by asbestos fibers and overexpression of plexin-A1 in nonmalignant mesothelial cells inhibits cell death after asbestos exposure.
  • [MeSH-major] Mesothelioma / pathology. NF-kappa B / genetics. Nerve Tissue Proteins / genetics. Pleural Neoplasms / pathology. Receptors, Cell Surface / genetics. Vascular Endothelial Growth Factor Receptor-2 / genetics

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  • (PMID = 19176370.001).
  • [ISSN] 1538-7445
  • [Journal-full-title] Cancer research
  • [ISO-abbreviation] Cancer Res.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / NF-kappa B; 0 / Nerve Tissue Proteins; 0 / PLXNA1 protein, human; 0 / RNA, Neoplasm; 0 / Receptors, Cell Surface; EC 2.7.10.1 / Vascular Endothelial Growth Factor Receptor-1; EC 2.7.10.1 / Vascular Endothelial Growth Factor Receptor-2
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78. Rezaei Kalantari H: [Malignant peritoneal mesothelioma: a case report]. Rev Med Liege; 2010 Sep;65(9):490-2
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  • [Title] [Malignant peritoneal mesothelioma: a case report].
  • I report two cases of malignant peritoneal mesothelioma.
  • Mesothelioma is mostly a pleural disease whether visceral or parietal.
  • Infra-diaphragmatic Mesothelioma accounts for only 10-20% of all mesotheliomas.
  • In over 80% of the cases the pathogenesis is related to asbestos and radiation exposure.
  • One of our two patients has non past history of exposure to asbestos.
  • Prognosis for patients with malignant peritoneal mesothelioma is very poor with a mean survival of 5,4 months versus 12.5 months for pleural mesothelioma.
  • Peritoneal mesothelioma, although rare, should be considered among the differential diagnosis of ascites differential diagnosis work up.
  • [MeSH-major] Mesothelioma / diagnosis. Peritoneal Neoplasms / diagnosis

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  • (PMID = 21086578.001).
  • [ISSN] 0370-629X
  • [Journal-full-title] Revue médicale de Liège
  • [ISO-abbreviation] Rev Med Liege
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Belgium
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79. Szeszenia-Dabrowska N: [Asbestos as a risk factor for pulmonary diseases]. Przegl Lek; 2008;65 Suppl 2:26-34
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  • [Title] [Asbestos as a risk factor for pulmonary diseases].
  • Asbestos is a recognised carcinogen, one of the most dangerous pollutants in the human environment.
  • This is associated with a huge accumulation of asbestos-containing materials that, as a result of their degradation, release fibres that are practically indestructible.
  • It is estimated that in recent years, asbestos was responsible for ca.
  • The pathogenic effects of asbestos on the respiratory system (the target organ) result from the inhalation of the respirable asbestos fibres suspended in the ambient air.
  • A specific feature of asbestos activity is that the pathologies appear even after cessation of the exposure; another feature is the development of mesotheliomas associated with the environmental exposure.
  • In Poland, the Act of 1997 banning the use of asbestos products has solved the problems associated with the occupational exposure in the asbestos processing industry, and prevented further accumulation of asbestos products.
  • However, problems of the environmental exposures to asbestos remain unsolved.
  • In spite that no worker has been occupationally exposed to asbestos during the recent 10 years, new cases of asbestosis, lung cancer pleural mesothelioma, non-malignant pleural diseases continue to be detected each year among the former workers of asbestos processing industry ("Amiantus" project).
  • This paper reports on the current status of asbestos-related diseases in Poland and worldwide, risk of the development of lung cancers and asbestos-specific mesotheliomas and gives recent recommendations for diagnosing and certification of asbestos-related diseases.
  • [MeSH-major] Asbestos / adverse effects. Occupational Exposure / prevention & control. Respiratory Tract Diseases / epidemiology

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  • (PMID = 19621651.001).
  • [ISSN] 0033-2240
  • [Journal-full-title] Przegla̧d lekarski
  • [ISO-abbreviation] Prz. Lek.
  • [Language] pol
  • [Publication-type] English Abstract; Journal Article; Review
  • [Publication-country] Poland
  • [Chemical-registry-number] 1332-21-4 / Asbestos
  • [Number-of-references] 17
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80. Sherwood AL, Mutsaers SE, Peeva VK, Robinson C, DeSilva CJ, Swanson NR, Lake RA: Spontaneously immortalized mouse mesothelial cells display characteristics of malignant transformation. Cell Prolif; 2008 Dec;41(6):894-908
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  • [Title] Spontaneously immortalized mouse mesothelial cells display characteristics of malignant transformation.
  • OBJECTIVES: Mesotheliomas occur in occult serous cavities after chronic exposure of mesothelial cells to asbestos fibres.
  • Comparative gene expression analysis demonstrated that spontaneously transformed cell lines were more closely related to neoplastic cells than to primary cells.
  • [MeSH-minor] Animals. Cell Aging / drug effects. Cell Line, Transformed. Cell Shape / drug effects. DNA / analysis. Down-Regulation / drug effects. Gene Deletion. Gene Expression Profiling. Genes, Tumor Suppressor. Humans. Intercellular Signaling Peptides and Proteins / pharmacology. Mesothelioma / genetics. Mice. Mice, Inbred C57BL

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  • (PMID = 19040568.001).
  • [ISSN] 1365-2184
  • [Journal-full-title] Cell proliferation
  • [ISO-abbreviation] Cell Prolif.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Intercellular Signaling Peptides and Proteins; 9007-49-2 / DNA
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81. Tsou MT, Luo JC: Porcelain factory worker with asbestos-related mesothelioma. J Formos Med Assoc; 2009 Oct;108(10):819-25
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  • [Title] Porcelain factory worker with asbestos-related mesothelioma.
  • Malignant mesothelioma is a rare tumor among the general population, but for people exposed to asbestos, the lifetime risk is high.
  • A chest X-ray revealed right-side pleural effusion; however, pleural biopsy from drainage treatment confirmed a diagnosis of malignant mesothelioma.
  • The specific characteristics of his work, making asbestos wallboards and gaskets, entailed working in high-temperature conditions with a high fine-particle content in the atmosphere.
  • The high working temperature caused asbestos debris and dust to fall down regularly from the wallboards, however, it was not until recently that the patient had started to wear personal protection.
  • Asbestos is a significant source of hazardous exposure in old buildings, and this case serves as a reminder of the importance of asbestos-related exposure history, which facilitated the correct diagnosis of pulmonary malignant mesothelioma.
  • Asbestos-containing materials that are now banned or regulated are still present in older buildings and remain an exposure hazard; they continue to be a serious health concern in many countries.

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  • [CommentIn] J Formos Med Assoc. 2010 May;109(5):389 [20497872.001]
  • (PMID = 19864204.001).
  • [ISSN] 0929-6646
  • [Journal-full-title] Journal of the Formosan Medical Association = Taiwan yi zhi
  • [ISO-abbreviation] J. Formos. Med. Assoc.
  • [Language] ENG
  • [Publication-type] Case Reports; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Singapore
  • [Chemical-registry-number] 1332-21-4 / Asbestos
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82. Creaney J, Musk AW, Robinson BW: Sensitivity of urinary mesothelin in patients with malignant mesothelioma. J Thorac Oncol; 2010 Sep;5(9):1461-6
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  • [Title] Sensitivity of urinary mesothelin in patients with malignant mesothelioma.
  • INTRODUCTION: Malignant mesothelioma (MM) is an aggressive, uniformly fatal tumor usually caused by exposure to asbestos.
  • As urine is less complex and less invasive to collect than serum and may be a more acceptable specimen for large-scale screening studies of asbestos-exposed individuals, we determined whether the sensitivity and specificity for MM could be improved by measuring soluble mesothelin in the urine.
  • METHODS: Soluble mesothelin concentrations were determined using the MESOMARK assay in concurrent serum and urine samples from 70 patients with pleural MM, 111 patients with asbestos-related lung or pleural disease, and 45 patients with benign nonasbestos-related lung and pleural disease.
  • [MeSH-major] Asbestos / adverse effects. Biomarkers, Tumor / urine. Membrane Glycoproteins / urine. Mesothelioma / urine. Pleural Neoplasms / urine

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  • (PMID = 20815094.001).
  • [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
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / GPI-Linked Proteins; 0 / Membrane Glycoproteins; 0 / mesothelin; 1332-21-4 / Asbestos; AYI8EX34EU / Creatinine
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83. Watanabe Y, Kojima T, Kagawa S, Uno F, Hashimoto Y, Kyo S, Mizuguchi H, Tanaka N, Kawamura H, Ichimaru D, Urata Y, Fujiwara T: A novel translational approach for human malignant pleural mesothelioma: heparanase-assisted dual virotherapy. Oncogene; 2010 Feb 25;29(8):1145-54
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  • [Title] A novel translational approach for human malignant pleural mesothelioma: heparanase-assisted dual virotherapy.
  • Malignant pleural mesothelioma (MPM) is a highly aggressive tumor that is related to asbestos exposure.
  • In this study, we show that telomerase-specific, replication-selective adenovirus OBP-301 can efficiently infect and kill human mesothelioma cells by viral replication.
  • Intrathoracic administration of virus significantly reduced the number and size of human mesothelioma tumors intrathoracically implanted into nu/nu mice.
  • A high-definition, fluorescence optical imaging system with an ultra-thin, flexible fibered microprobe clearly detected intracellular replication of green fluorescent protein-expressing oncolytic virus in intrathoracically established mesothelioma tumors.
  • Our results suggest that intrathoracic dual virotherapy with telomerase-specific oncolytic adenovirus in combination with heparanase-expressing adenovirus may be efficacious in the prevention and treatment of pleural dissemination of human malignant mesothelioma.
  • [MeSH-major] Adenoviridae / genetics. Genetic Therapy. Glucuronidase / genetics. Mesothelioma / therapy. Oncolytic Virotherapy. Pleural Neoplasms / therapy. Transfection / methods


84. Wang Y, Rishi AK, Puliyappadamba VT, Sharma S, Yang H, Tarca A, Dou QP, Lonardo F, Ruckdeschel JC, Pass HI, Wali A: Targeted proteasome inhibition by Velcade induces apoptosis in human mesothelioma and breast cancer cell lines. Cancer Chemother Pharmacol; 2010 Aug;66(3):455-66
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  • [Title] Targeted proteasome inhibition by Velcade induces apoptosis in human mesothelioma and breast cancer cell lines.
  • Malignant pleural mesothelioma (MPM) is an asbestos-related tumor of the thoracic pleura that lacks effective treatment options.
  • Pretreatment of mesothelioma cells with Velcade showed synergistic effect with cisplatin combination regimens.
  • High-throughput gene expression profiling among Velcade treated and untreated mesothelioma cell lines resulted in identification of novel transducers of apoptosis such as CARP-1, XAF1, and Troy proteins.
  • This pilot study has paved way for further in-depth analysis of the downstream target molecules associated with presensitization of mesothelioma cells in finding effective therapeutic treatment options for both mesothelioma and recalcitrant breast cancers.
  • [MeSH-major] Antineoplastic Combined Chemotherapy Protocols / pharmacology. Apoptosis / drug effects. Breast Neoplasms / drug therapy. Mesothelioma / drug therapy. Protease Inhibitors / pharmacology


85. Amati M, Tomasetti M, Scartozzi M, Mariotti L, Alleva R, Pignotti E, Borghi B, Valentino M, Governa M, Neuzil J, Santarelli L: Profiling tumor-associated markers for early detection of malignant mesothelioma: an epidemiologic study. Cancer Epidemiol Biomarkers Prev; 2008 Jan;17(1):163-70
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  • [Title] Profiling tumor-associated markers for early detection of malignant mesothelioma: an epidemiologic study.
  • Improved detection methods for diagnosis of asymptomatic malignant mesothelioma (MM) are essential for an early and reliable detection and treatment of this type of neoplastic disease.
  • Ninety-four asbestos-exposed subjects defined at high risk, 22 patients with MM, and 54 healthy subjects were recruited for evaluation of the clinical significance of 8-hydroxy-2'-deoxyguanosine (8OHdG) in WBCs and plasma concentrations of soluble mesothelin-related peptides (SMRPs), angiogenic factors [platelet-derived growth factor beta, hepatocyte growth factor, basic fibroblast growth factor, and vascular endothelial growth factor beta (VEGFbeta)], and matrix proteases [matrix metalloproteinase (MMP) 2, MMP9, tissue inhibitor of metalloproteinase (TIMP) 1, and TIMP2] for potential early detection of MM.
  • The area under receiver operating characteristic (ROC) curves indicate that 8OHdG levels can discriminate asbestos-exposed subjects from healthy controls but not from MM patients.
  • Significant area under ROC curve values were found for SMRPs, discriminating asbestos-exposed subjects from MM patients but not from healthy controls.
  • The combination of blood biomarkers and radiographic findings could be used to stratify the risk of mesothelioma in asbestos-exposed populations.
  • [MeSH-major] Asbestosis / blood. Biomarkers, Tumor / blood. Mesothelioma / blood

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  • (PMID = 18199721.001).
  • [ISSN] 1055-9965
  • [Journal-full-title] Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology
  • [ISO-abbreviation] Cancer Epidemiol. Biomarkers Prev.
  • [Language] eng
  • [Publication-type] Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Angiogenesis Inducing Agents; 0 / Biomarkers, Tumor; 0 / Tissue Inhibitor of Metalloproteinase-1; 127497-59-0 / Tissue Inhibitor of Metalloproteinase-2; 88847-89-6 / 8-oxo-7-hydrodeoxyguanosine; EC 3.4.24.24 / Matrix Metalloproteinase 2; EC 3.4.24.35 / Matrix Metalloproteinase 9; G9481N71RO / Deoxyguanosine
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86. Scattone A, Pennella A, Gentile M, Musti M, Nazzaro P, Buonadonna AL, Marzullo A, Cavone D, Pollice L, Serio G: Comparative genomic hybridisation in malignant deciduoid mesothelioma. J Clin Pathol; 2006 Jul;59(7):764-9
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  • [Title] Comparative genomic hybridisation in malignant deciduoid mesothelioma.
  • BACKGROUND: Malignant deciduoid mesothelioma is a rare variant of epithelioid mesothelioma.
  • This tumour generally has poor prognosis, and can be asbestos related.
  • AIM: To identify peculiar genetic changes responsible for critical phases in pathogenesis of malignant deciduoid mesothelioma and their prognostic relevance.
  • METHODS: Comparative genomic hybridisation was carried out in six cases of malignant pleural deciduoid mesothelioma, four sporadic and two familial.
  • All cases were found to be asbestos related.
  • The clinical outcome for this mesothelioma subtype is predicted by the number of losses.
  • [MeSH-major] Chromosome Aberrations. Mesothelioma / genetics. Pleural Neoplasms / genetics
  • [MeSH-minor] Adult. Aged. Asbestos / adverse effects. Female. Humans. Image Processing, Computer-Assisted. Immunoenzyme Techniques. Male. Middle Aged. Nucleic Acid Hybridization / methods. Occupational Diseases / etiology. Occupational Diseases / genetics. Occupational Diseases / pathology. Prognosis. Retrospective Studies

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  • (PMID = 16569690.001).
  • [ISSN] 0021-9746
  • [Journal-full-title] Journal of clinical pathology
  • [ISO-abbreviation] J. Clin. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
  • [Chemical-registry-number] 1332-21-4 / Asbestos
  • [Other-IDs] NLM/ PMC1860431
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87. Guled M, Lahti L, Lindholm PM, Salmenkivi K, Bagwan I, Nicholson AG, Knuutila S: CDKN2A, NF2, and JUN are dysregulated among other genes by miRNAs in malignant mesothelioma -A miRNA microarray analysis. Genes Chromosomes Cancer; 2009 Jul;48(7):615-23
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  • [Title] CDKN2A, NF2, and JUN are dysregulated among other genes by miRNAs in malignant mesothelioma -A miRNA microarray analysis.
  • Malignant mesothelioma (MM) is an aggressive cancer arising from mesothelial cells, mainly due to former asbestos exposure.
  • Regarding risk factors such as smoking status and asbestos exposure, significantly differentially expressed miRNAs were identified in smokers versus nonsmokers (miR-379, miR-301a, miR-299-3p, miR-455-3p, and miR-127-3p), but not in asbestos-exposed patients versus nonexposed ones.
  • This could be related to the method of assessment of asbestos exposure as asbestos remains to be the main contributor to the development of MM.
  • [MeSH-major] Cyclin-Dependent Kinase Inhibitor p16 / genetics. Gene Expression Regulation, Neoplastic. Mesothelioma / genetics. MicroRNAs / genetics. Neurofibromin 2 / genetics. Proto-Oncogene Proteins c-jun / genetics
  • [MeSH-minor] Aged. Asbestos / poisoning. Chromosomes, Human. Cluster Analysis. Female. Gene Expression Profiling / methods. Humans. Male. Middle Aged. Oligonucleotide Array Sequence Analysis / methods. Risk Factors. Smoking / genetics. Smoking / metabolism. Survival Analysis


88. Kurata S, Ishibashi M, Azuma K, Kaida H, Takamori S, Fujimoto K, Kobayashi M, Hirose Y, Aizawa H, Hayabuchi N: Preliminary study of positron emission tomography/computed tomography and plasma osteopontin levels in patients with asbestos-related pleural disease. Jpn J Radiol; 2010 Jul;28(6):446-52
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  • [Title] Preliminary study of positron emission tomography/computed tomography and plasma osteopontin levels in patients with asbestos-related pleural disease.
  • PURPOSE: The aim of this study was to compare the results of semiquantitative analysis by(18)F-fluorodeoxyglucose positron emission tomography/computed tomography (PET/CT) with plasma osteopontin levels in the same asbestos-related pleural disease population.
  • MATERIALS AND METHODS: A total of 17 patients with asbestos-related pleural disease were prospectively recruited.
  • RESULTS: Malignant pleural mesothelioma (MPM) was histologically proven in 6 patients, and 11 patients had proven benign asbestos-related pleural diseases (7 pleural plaques, 4 asbestos pleurisy).
  • Significant differences in SUVmax were found between patients with MPM and those with asbestos pleurisy (P = 0.031) and between patients with MPM and those with pleural plaques (P = 0.012).
  • A significant difference was found in the plasma osteopontin levels between patients with asbestos pleurisy and patients with pleural plaques (Bonferroni correction, P = 0.024).
  • The SUVmax in patients with benign asbestos-related diseases was statistically positively correlated with plasma osteopontin in the same group (Spearman's r = 0.75, P < 0.05).
  • CONCLUSION: PET/CT might be more helpful than plasma osteopontin for distinguishing benign asbestos-related pleural diseases from MPM, and the SUVmax in benign asbestos-related pleural diseases may reflect changes in pleural inflammation.
  • [MeSH-major] Asbestos / toxicity. Mesothelioma / diagnostic imaging. Osteopontin / blood. Pleural Diseases / diagnostic imaging. Positron-Emission Tomography / methods. Tomography, Spiral Computed / methods

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  • (PMID = 20661695.001).
  • [ISSN] 1867-108X
  • [Journal-full-title] Japanese journal of radiology
  • [ISO-abbreviation] Jpn J Radiol
  • [Language] eng
  • [Publication-type] Comparative Study; Evaluation Studies; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Japan
  • [Chemical-registry-number] 0 / Radiopharmaceuticals; 0Z5B2CJX4D / Fluorodeoxyglucose F18; 106441-73-0 / Osteopontin; 1332-21-4 / Asbestos
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89. Munkholm-Larsen S, Cao CQ, Yan TD: Malignant peritoneal mesothelioma. World J Gastrointest Surg; 2009 Nov 30;1(1):38-48
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  • [Title] Malignant peritoneal mesothelioma.
  • Malignant mesothelioma is a highly aggressive neoplasm.
  • The incidence of malignant mesothelioma is increasing worldwide.
  • Diffuse malignant peritoneal mesothelioma (DMPM) represents one-fourth of all mesotheliomas.
  • Association of asbestos exposure with DMPM has been observed, especially in males.
  • This remarkable improvement in survival has prompted new search into the medical science related to DMPM, a disease previously ignored as uninteresting.

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  • (PMID = 21160794.001).
  • [ISSN] 1948-9366
  • [Journal-full-title] World journal of gastrointestinal surgery
  • [ISO-abbreviation] World J Gastrointest Surg
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] China
  • [Other-IDs] NLM/ PMC2999110
  • [Keywords] NOTNLM ; Asbestos / Cisplatin / Cytoreductive surgery / Doxorubicin / Intraperitoneal chemotherapy / Mesothelin / Pemetrexed / Peritoneal mesothelioma / Peritonectomy
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91. Montomoli L, Spisso M, Romeo R, Spina D, Ghiribelli C, Sartorelli P: [Work related mesothelioma: analysis of cases discovered at the Section for Occupational Medicine and Toxicology of Siena University during the years 2000-2007]. G Ital Med Lav Ergon; 2007 Jul-Sep;29(3 Suppl):332-3
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Work related mesothelioma: analysis of cases discovered at the Section for Occupational Medicine and Toxicology of Siena University during the years 2000-2007].
  • This study focuses on the spread of mesothelioma in Siena.
  • The association between malignant masothelioma and exposure to asbestos was deduced by the occupational history.
  • The mesothelioma was noted both in traditional industries and other jobs such as the chain of manifacture, plumbers, electricians, carpenters, installers of asbestos insulation and construction workers.
  • Thus it is possible to find other malignant and nonmalignant asbestos-related diseases more frequently than mesothelioma.
  • [MeSH-major] Mesothelioma / epidemiology. Occupational Diseases / epidemiology. Pleural Neoplasms / epidemiology
  • [MeSH-minor] Aged. Asbestos / adverse effects. Female. Humans. Italy. Male. Universities

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  • (PMID = 18409711.001).
  • [ISSN] 1592-7830
  • [Journal-full-title] Giornale italiano di medicina del lavoro ed ergonomia
  • [ISO-abbreviation] G Ital Med Lav Ergon
  • [Language] ita
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Italy
  • [Chemical-registry-number] 1332-21-4 / Asbestos
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92. Otsuki T, Maeda M, Murakami S, Hayashi H, Miura Y, Kusaka M, Nakano T, Fukuoka K, Kishimoto T, Hyodoh F, Ueki A, Nishimura Y: Immunological effects of silica and asbestos. Cell Mol Immunol; 2007 Aug;4(4):261-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Immunological effects of silica and asbestos.
  • Silicosis patients (SILs) and patients who have been exposed to asbestos develop not only respiratory diseases but also certain immunological disorders.
  • In addition, malignant complications such as lung cancer and malignant mesothelioma often occur in patients exposed to asbestos, and may be involved in the reduction of tumor immunity.
  • A brief summary of our investigations related to the immunological effects of silica/asbestos is presented.
  • Recent advances in immunomolecular studies led to detailed analyses of the immunological effects of asbestos and silica.
  • Both affect immuno-competent cells and these effects may be associated with the pathophysiological development of complications in silicosis and asbestos-exposed patients such as the occurrence of autoimmune disorders and malignant tumors, respectively.
  • In particular, as the incidence of asbestos-related malignancies is increasing and such malignancies have been a medical and social problem since the summer of 2005 in Japan, efforts should be focused on developing a cure for these diseases to eliminate nationwide anxiety.
  • [MeSH-major] Asbestos / immunology. Silicon Dioxide / immunology

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  • (PMID = 17764616.001).
  • [ISSN] 1672-7681
  • [Journal-full-title] Cellular & molecular immunology
  • [ISO-abbreviation] Cell. Mol. Immunol.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't; Review
  • [Publication-country] China
  • [Chemical-registry-number] 0 / Antigens, CD; 0 / Autoantibodies; 1332-21-4 / Asbestos; 7631-86-9 / Silicon Dioxide
  • [Number-of-references] 72
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93. Betti M, Neri M, Ferrante D, Landi S, Biava A, Gemignani F, Bertolotti M, Mirabelli D, Padoan M, Ugolini D, Botta M, Bonassi S, Magnani C, Dianzani I: Pooled analysis of NAT2 genotypes as risk factors for asbestos-related malignant mesothelioma. Int J Hyg Environ Health; 2009 May;212(3):322-9
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  • [Title] Pooled analysis of NAT2 genotypes as risk factors for asbestos-related malignant mesothelioma.
  • Malignant mesothelioma (MM) is a rare and aggressive tumor of the pleura.
  • The most important causal factor for the development of MM is occupational exposure to asbestos.
  • To ascertain the role of NAT2 genotype, we performed a study on 252 MM patients and 262 controls recruited in two Northern Italy areas that were characterized by high asbestos exposure, due to intense industrial activities (an asbestos cement factory in Casale Monferrato, mainly shipyards and refineries in Liguria).
  • NAT2 fast acetylator genotypes showed an increased OR, although not statistically significant, both in asbestos-exposed subjects (OR=1.47; 95% CI=0.96-2.26) and in the entire population (OR=1.38; 95% CI=0.93-2.04).
  • [MeSH-major] Arylamine N-Acetyltransferase / genetics. Asbestos / adverse effects. Carcinogens. Genetic Predisposition to Disease. Mesothelioma / genetics. Pleural Neoplasms / genetics. Polymorphism, Genetic

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  • (PMID = 18838334.001).
  • [ISSN] 1618-131X
  • [Journal-full-title] International journal of hygiene and environmental health
  • [ISO-abbreviation] Int J Hyg Environ Health
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Carcinogens; 1332-21-4 / Asbestos; EC 2.3.1.5 / Arylamine N-Acetyltransferase; EC 2.3.1.5 / NAT2 protein, human
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94. Marinaccio A, Binazzi A, Cauzillo G, Chellini E, De Zotti R, Gennaro V, Menegozzo M, Mensi C, Merler E, Mirabelli D, Musti M, Pannelli F, Romanelli A, Scarselli A, Tosi S, Tumino R, Nesti M, Gruppo di lavoro ReNaM: [Epidemiological surveillance of malignant mesothelioma cases in Italy: incidence and asbestos exposure figures by the Italian mesothelioma registry (ReNaM)]. Epidemiol Prev; 2007 Jul-Aug;31(4 Suppl 1):23-6
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  • [Title] [Epidemiological surveillance of malignant mesothelioma cases in Italy: incidence and asbestos exposure figures by the Italian mesothelioma registry (ReNaM)].
  • The Study describes the epidemiological surveillance of mesothelioma cases carried out by the Italian mesothelioma register (ReNaM).
  • A Regional Operating Centre (COR) is present in nearly all Italian regions (17 out of 20) and it collects malignant mesothelioma cases and investigate the modalities of asbestos exposure by using a structured questionnaire.
  • The register produces malignant mesothelioma incidence measures and analyses of the modalities of the asbestos exposure.
  • The standardized incidence rate of malignant mesothelioma in 2001 was 2.98 (in 100,000 inhabitants) among men and 0.98 among women; a professional (certain, probable, possible) exposure has been detected in 67.4% of defined cases.
  • In addition to the conventional sectors (shipbuilding, railways repair and demolition, asbestos-cement production), also textile, building, transport, chemical and glass industries, petroleum and sugar refineries, electricity production and distribution plants are getting involved.
  • Despite the absence of some regions completing the national coverage and the non homogeneity in collecting and coding data, the epidemiological surveillance of malignant mesothelioma carried out by ReNaM is an important tool for the scientific knowledge and the prevention of asbestos-related diseases.
  • [MeSH-major] Asbestos / adverse effects. Mesothelioma / epidemiology. Mesothelioma / etiology. Occupational Diseases / epidemiology. Occupational Diseases / etiology. Occupational Exposure / adverse effects. Pleural Neoplasms / epidemiology. Pleural Neoplasms / etiology


95. Chapman EA, Thomas PS, Yates DH: Breath analysis in asbestos-related disorders: a review of the literature and potential future applications. J Breath Res; 2010 Sep;4(3):034001
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Breath analysis in asbestos-related disorders: a review of the literature and potential future applications.
  • Asbestos usage was very common worldwide in the last century and continues in several countries today.
  • Several diseases occur due to asbestos exposure, including malignant tumours such as malignant mesothelioma of the pleura and lung cancer, which have a very poor prognosis.
  • Asbestos inhalation may also result in more benign conditions such as asbestosis (or pulmonary fibrosis due to asbestos), pleural plaques and pleural thickening.
  • It is predicted that asbestos-associated mortality and morbidity will continue to increase, but methods for diagnosing asbestos-related disease are currently invasive and unsuitable for an increasingly elderly population.
  • [MeSH-major] Asbestos / analysis. Asbestosis / diagnosis

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  • (PMID = 21383477.001).
  • [ISSN] 1752-7163
  • [Journal-full-title] Journal of breath research
  • [ISO-abbreviation] J Breath Res
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't; Review
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Biomarkers; 1332-21-4 / Asbestos
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96. Greillier L, Astoul P: Mesothelioma and asbestos-related pleural diseases. Respiration; 2008;76(1):1-15
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Mesothelioma and asbestos-related pleural diseases.
  • At present, the use of asbestos is not regulated at a worldwide scale.
  • Moreover, there is a latency period between asbestos exposure and the manifestations of asbestos-related diseases.
  • Consequently, pulmonologists are still dealing with consequences of asbestos exposure, which mainly occur at the pleural surface.
  • The aim of this review is to provide an overview of asbestos-related pleural diseases.
  • We summarized the most relevant data for the diagnosis and the management of benign asbestos pleural effusions, pleural plaques, diffuse pleural thickening and rounded atelectasis.
  • Special attention is dedicated to malignant pleural mesothelioma, given the challenging issues of this disease, the recent advances in its management and the dynamism of research in this area.
  • [MeSH-major] Asbestosis. Mesothelioma. Pleural Diseases. Pleural Neoplasms

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  • [Copyright] 2008 S. Karger AG, Basel.
  • (PMID = 18583923.001).
  • [ISSN] 1423-0356
  • [Journal-full-title] Respiration; international review of thoracic diseases
  • [ISO-abbreviation] Respiration
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] Switzerland
  • [Number-of-references] 189
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97. Takemura Y, Satoh M, Satoh K, Hamada H, Sekido Y, Kubota S: High dose of ascorbic acid induces cell death in mesothelioma cells. Biochem Biophys Res Commun; 2010 Apr 2;394(2):249-53
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  • [Title] High dose of ascorbic acid induces cell death in mesothelioma cells.
  • Malignant mesothelioma is an asbestos-related fatal disease with no effective cure.
  • We studied whether high dose of ascorbic acid induced cell death of four human mesothelioma cell lines.
  • High dose of ascorbic acid induced cell death of all mesothelioma cell lines in a dose-dependent manner.
  • In vivo experiment, intravenous administration of ascorbic acid significantly decreased the growth rate of mesothelioma tumor inoculated in mice.
  • These data suggest that ascorbic acid may have benefits for patients with mesothelioma.
  • [MeSH-major] Apoptosis. Ascorbic Acid / administration & dosage. Mesothelioma / drug therapy

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  • [Copyright] 2010 Elsevier Inc. All rights reserved.
  • (PMID = 20171954.001).
  • [ISSN] 1090-2104
  • [Journal-full-title] Biochemical and biophysical research communications
  • [ISO-abbreviation] Biochem. Biophys. Res. Commun.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Reactive Oxygen Species; PQ6CK8PD0R / Ascorbic Acid
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98. Creaney J, Olsen NJ, Brims F, Dick IM, Musk AW, de Klerk NH, Skates SJ, Robinson BW: Serum mesothelin for early detection of asbestos-induced cancer malignant mesothelioma. Cancer Epidemiol Biomarkers Prev; 2010 Sep;19(9):2238-46
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  • [Title] Serum mesothelin for early detection of asbestos-induced cancer malignant mesothelioma.
  • BACKGROUND: Malignant mesothelioma is an aggressive, almost uniformly fatal tumor, primarily caused by exposure to asbestos.
  • Since the recent discovery that serum mesothelin is a sensitive and highly specific biomarker for mesothelioma, one of the key issues raised is whether mesothelin levels represent a useful screening test for asbestos-exposed at-risk individuals.
  • In this study, soluble mesothelin was determined in sequential serum samples collected from asbestos-exposed individuals before the development of mesothelioma.
  • METHODS: Archival serum samples from 106 individuals who developed mesothelioma, 99 asbestos-exposed individuals from the Wittenoom Cancer Surveillance Program, and 109 non-asbestos-exposed individuals from the Busselton Health Survey were identified.
  • RESULTS: Longitudinal mesothelin levels determined in healthy asbestos-exposed individuals over a period of 4 years were stable (Pearson's r = 0.96; P < 0.0001).
  • There was no correlation between mesothelin concentration and cumulative asbestos exposure.
  • Mesothelin concentrations were greater than the threshold value of 2.5 nmol/L in the penultimate serum sample before the diagnosis of mesothelioma in 17 of 106 people.
  • CONCLUSION: In a population with a high pretest probability of developing mesothelioma, the serum biomarker mesothelin is elevated in absolute terms in 15% and in relative terms in 40% of the group.
  • [MeSH-major] Asbestos / adverse effects. Biomarkers, Tumor / blood. Membrane Glycoproteins / blood. Mesothelioma / blood. Mesothelioma / etiology

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  • [Copyright] (c)2010 AACR.
  • (PMID = 20651076.001).
  • [ISSN] 1538-7755
  • [Journal-full-title] Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology
  • [ISO-abbreviation] Cancer Epidemiol. Biomarkers Prev.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / GPI-Linked Proteins; 0 / Membrane Glycoproteins; 0 / mesothelin; 1332-21-4 / Asbestos
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99. Petazzi A, Gaudiello F, Canti Z, Mensi C: [Cluster cases of malignant pleural mesothelioma in an oil factory]. Med Lav; 2005 Sep-Oct;96(5):440-4
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  • [Title] [Cluster cases of malignant pleural mesothelioma in an oil factory].
  • No cases are reported in literature of asbestos related disease in subjects who worked in oil factories.
  • Nevertheless the structure and organization of the workplace, which is similar to that of sugar refineries, where cases of malignant mesothelioma have been described (moreover in workers employed in running and maintenance of the plants), led to the assumption that even in oil factories asbestos for the insulation of pipes and boilers could be present.
  • OBJECTIVES: To describe 3 cases of Malignant Mesothelioma that occurred in workers of the same oil factory.
  • METHODS: Since this occupational sector is not conventionally known for asbestos exposure the Local Health Unit and the Lombardy Mesothelioma Registry decided to investigate this industrial plant.
  • RESULTS: Following examination of the archives of the Local Health Unit and inspection of the plant, an environmental asbestos contamination (pipes and boilers) was found.
  • This underlines the importance of close cooperation with Local Health Units of occupational medicine and the Regional Mesothelioma Registry in the study and acknowledgment of cases which would otherwise not have been recognized, with consequent loss of precious information.
  • [MeSH-major] Air Pollutants, Occupational / adverse effects. Asbestos / adverse effects. Chemical Industry. Mesothelioma / epidemiology. Occupational Diseases / epidemiology. Petroleum. Pleural Neoplasms / epidemiology


100. Cristaudo A, Foddis R, Bonotti A, Simonini S, Vivaldi A, Guglielmi G, Ambrosino N, Canessa PA, Chella A, Lucchi M, Mussi A, Mutti L: Comparison between plasma and serum osteopontin levels: usefulness in diagnosis of epithelial malignant pleural mesothelioma. Int J Biol Markers; 2010 Jul-Sep;25(3):164-70
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  • [Title] Comparison between plasma and serum osteopontin levels: usefulness in diagnosis of epithelial malignant pleural mesothelioma.
  • BACKGROUND: A potential role of serum osteopontin (OPN) and serum mesothelin-related peptide (SMRP) in the diagnosis of malignant pleural mesothelioma (MPM) has been recently reported.
  • Our study aimed to evaluate the influence of preanalytic variables on serum and plasma OPN, to compare serum and plasma OPN in the same population, and to assess whether OPN levels can aid in the diagnostic distinction of patients with MPM versus benign respiratory disease (BRD) and healthy subjects exposed to asbestos.
  • We measured OPN in 239 plasma samples from 207 asbestos-exposed subjects including 94 healthy controls and 113 subjects with BRD, and 32 patients with epithelial MPM, employing a commercially available ELISA.
  • Within the control group no significant correlation was observed between age, duration of asbestos exposure, pack-years in current smokers, lung function or imaging parameters and plasma or serum OPN.
  • CONCLUSIONS: These data suggest that plasma OPN and serum OPN are not influenced by confounding factors such as age, smoking habits and asbestos exposure.
  • [MeSH-major] Asbestos / adverse effects. Biomarkers, Tumor / blood. Mesothelioma / blood. Osteopontin / blood. Pleural Neoplasms / blood. Specimen Handling

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  • (PMID = 20878622.001).
  • [ISSN] 1724-6008
  • [Journal-full-title] The International journal of biological markers
  • [ISO-abbreviation] Int. J. Biol. Markers
  • [Language] eng
  • [Publication-type] Comparative Study; Controlled Clinical Trial; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 106441-73-0 / Osteopontin; 1332-21-4 / Asbestos
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