Genetic polymorphisms of cytochrome P450 2A6 in a case-control study on lung cancer in a French population

被引:92
|
作者
Loriot, MA
Rebuissou, S
Oscarson, M
Cenée, S
Miyamoto, M
Ariyoshi, N
Kamataki, T
Hémon, D
Beaune, P
Stücker, I
机构
[1] Univ Paris 05, INSERM, U490, F-75006 Paris, France
[2] Karolinska Inst, Inst Environm Med, Div Mol Toxicol, S-10401 Stockholm, Sweden
[3] INSERM, U170, Villejuif, France
[4] Hokkaido Univ, Grad Sch Pharmaceut Sci, Div Pharmacobiodynam, Lab Drug Metab, Sapporo, Hokkaido 060, Japan
来源
PHARMACOGENETICS | 2001年 / 11卷 / 01期
关键词
cytochrome P450 2A6; genetic polymorphism; lung cancer; tobacco consumption;
D O I
10.1097/00008571-200102000-00005
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Cytochrome P450 2A6 (CYP2A6) is involved in the C-oxidation of nicotine and in the metabolic activation of tobacco nitrosamines. Recent data have suggested that CYP2A6 genetic polymorphisms might play a role in tobacco dependence and consumption as well as in lung cancer risk, However, the previously published studies were based on a genotyping method that overestimated the frequencies of deficient alleles, leading to misclassification for the CYP2A6 genotype, In this study, we genotyped DNA from 244 lung cancer patients and from 250 control subjects for CYP2A6 (wild-type allele CYP2A6*1, and two deficient alleles: CYP2A6*2, and CYP2A6*4, the latter corresponding to a deletion of the gene) using a more specific procedure. In this Caucasian population, we found neither a relation between genetically impaired nicotine metabolism and cigarette consumption, nor any modification of lung cancer risk related to the presence of defective CYP2A6 alleles (odds ratio = 1.1, 95% confidence interval = 0.7-1.9). Pharmacogenetics 11:39-44 (C) 2001 Lippincott Williams & Wilkins.
引用
收藏
页码:39 / 44
页数:6
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