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.
Original language | English (US) |
---|---|
Pages (from-to) | 503-511 |
Number of pages | 9 |
Journal | Pharmacogenetics |
Volume | 8 |
Issue number | 6 |
DOIs | |
State | Published - 1998 |
Keywords
- CYP1A1
- CYP2E1
- GSTM1
- Lung cancer
- p53
ASJC Scopus subject areas
- Genetics
- Pharmacology, Toxicology and Pharmaceutics(all)