| Literature DB >> 9918134 |
R M Przygodzki1, W P Bennett, D G Guinee, M A Khan, A Freedman, P G Shields, W D Travis, J R Jett, H Tazelaar, P Pairolero, V Trastek, L A Liotta, C C Harris, N E Caporaso.
Abstract
p53 mutation status was analysed in relation to DNA polymorphisms of GSTM1, CYP1A1 and CYP2E1 from 105 surgically resected non-small cell lung cancer cases. Demographic factors, smoking, occupation, family history, tumour histology, grade and stage were taken into account. p53 mutations, detected either directly by DNA sequencing (P = 0.04, adjusted for smoking) or indirectly by immunostaining (P = 0.06), were overrepresented among CYP1A1 variants. Mutations in exon 8 and transitions at CpG sites in the p53 gene were favoured in this subset. There was no relation between the individual gene polymorphisms or p53 mutations and disease-free survival by Kaplan-Meier analysis. The finding of excess CYP1A1 heterozygotes in individuals with p53 mutations after adjustment for smoking suggests that CYP1A1 activation contributes to lung cancer via p53 inactivation.Entities:
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Year: 1998 PMID: 9918134 DOI: 10.1097/00008571-199812000-00007
Source DB: PubMed Journal: Pharmacogenetics ISSN: 0960-314X