Analysis of K-Ras and p53 Mutations in Mesotheliomas from Humans and Rats Exposed to Asbestos
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2000/06/22
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Description:Malignant mesothelioma is known to be associated with asbestos exposure. However, the mechanism of mesothelial carcinogenesis in relation to the activation of proto-oncogenes or inactivation of tumor suppressor genes remains unclear. In this study, the PCR-Primer Introduced Restriction Site (PCR-PIRS) assay was employed to examine mutations in the K-ras proto-oncogene in mesothelioma tissues from workers exposed to asbestos and from rats treated with asbestos. Mutations in exons 5-8 of the p53 tumor suppressor gene were determined by direct DNA sequence analysis. Results of the PCR-PIRS analysis revealed no mutations in codons 12, 13 or 61 of the K-ras gene in any of the 17 human or 22 rat mesothelioma tissue samples. These results were confirmed by direct DNA sequence analysis. No mutations were found in exons 5-8 of the p53 gene in any of the mesothelioma tissue samples analyzed. These results and the results reported by others indicate that the K-ras proto-oncogene and p53 tumor suppressor gene may not play a critical role in the induction of mesothelioma by asbestos either in humans or in rats. [Description provided by NIOSH]
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ISSN:0027-5107
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Pages in Document:87-92
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Volume:468
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Issue:1
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NIOSHTIC Number:nn:20020766
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Citation:Mutat Res 2000 Jun; 468(1):87-92
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Contact Point Address:Toxicology and Molecular Biology Branch, National Institute for Occupational Safety and Health, HELD, NIOSH, m/s 3014, 1095 Willowdale Road, Morgantown, WV 26505-2888, USA
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Email:too2@cdc.gov
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Federal Fiscal Year:2000
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Peer Reviewed:True
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Source Full Name:Mutation Research
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Main Document Checksum:urn:sha-512:f802d4e2b4dd48eaa3c0a0ccc2a38e4a20dd41bbcdaf59eb10bc3d054adbed8128eb621d7651855304cd9186cedb0df07e609fac96698fd20c0ad105f483d45b
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