Evaluation of CYP2A6 genetic polymorphisms as determinants of smoking behavior and tobacco-related lung cancer risk in male Japanese smokers

被引:152
作者
Fujieda, M [1 ]
Yamazaki, H
Saito, T
Kiyotani, K
Gyamfi, MA
Sakurai, M
Dosaka-Akita, H
Sawamura, Y
Yokota, J
Kunitoh, H
Kamataki, T
机构
[1] Hokkaido Univ, Grad Sch Pharmaceut Sci, Lab Drug Metab, Div Pharmacobiodynam, Sapporo, Hokkaido 0600812, Japan
[2] Kumamoto Univ, Grad Sch Clin Pharm, Div Pharmacol & Therapeut, Kumamoto 8620973, Japan
[3] Hokkaido Univ, Dept Med Oncol, Grad Sch Med, Sapporo, Hokkaido 0608638, Japan
[4] Maruyama Clin, Sapporo, Hokkaido 0640820, Japan
[5] Natl Canc Ctr, Res Inst, Div Biol, Tokyo 1040045, Japan
[6] Natl Canc Ctr, Dept Internal Med & Thorac Oncol, Tokyo 1040045, Japan
关键词
D O I
10.1093/carcin/bgh258
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We reported previously that subjects homozygous for the cytochrome P450 2A6 (CYP2A6) (*)4 have a lower risk of lung cancer. The purpose of this study was to clarify whether or not the alterations of smoking behavior and risk for lung cancer could be found in subjects possessing novel CYP2A6 variants discovered recently. An epidemiological study was performed with 1094 cases and 611 controls in male Japanese smokers. It was found that the amounts of daily cigarette consumption in subjects who harbored CYP2A6(*)4/(*)7, (*)4/(*)10, (*)7/(*)7, (*)7/(*)9 and (*)4/(*)4 genotypes were significantly less than those in subjects carrying the (*)1/(*)1 genotype (P < 0.01). Even after adjustment with cigarette consumption, the adjusted odds ratios (ORs) for lung cancer were significantly lower in subjects who harbored CYP2A6(*)1/(*)4, (*)1/(*)7, (*)1/(*)9, (*)1/(*)10, (*)4/(*)4, (*)4/(*)7, (*)4/(*)9, (*)7/(*)7 and (*)7/(*)9 genotypes than those who possessed the (*)1/(*)1 genotype (P < 0.05). When participants were classified into four groups according to the CYP2A6 genotypes, group 1 ((*)1/(*)1), group 2 (heterozygotes for the (*)1 and a variant allele), group 3 (heterozygotes and homozygotes for variant alleles except for (*)4/(*)4) and group 4 ((*)4/(*)4), lung cancer risk was found to be less in subjects with the variant of CYP2A6 alleles {group 2, OR of 0.59 [95% confidence interval (CI), 0.44-0.79]; group 3, OR of 0.52 (95% CI, 0.37-0.72); group 4, OR of 0.30 (95% CI, 0.16-0.57)}. The reduced risk for lung cancer was seen more clearly in heavy smokers than in light smokers. Additional stratification analysis showed that the ORs for squamous cell carcinoma (OR of 0.07) and small cell carcinoma (OR of 0.10) were lower than that of adenocarcinoma (OR of 0.39) in group 4. These results suggest that the CYP2A6 is one of the principal determinants affecting not only smoking behavior but also susceptibility to tobacco-related lung cancer.
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页码:2451 / 2458
页数:8
相关论文
共 56 条
[1]  
Ariyoshi N, 2002, CANCER EPIDEM BIOMAR, V11, P890
[2]   Characterization of a genotype previously designated as CYP2A6 D-type:: CYP2A6*4B, another entire gene deletion allele of the CYP2A6 gene in Japanese [J].
Ariyoshi, N ;
Sekine, H ;
Saito, K ;
Kamataki, T .
PHARMACOGENETICS, 2002, 12 (06) :501-504
[3]   A novel single nucleotide polymorphism altering stability and activity of CYP2A6 [J].
Ariyoshi, N ;
Sawamura, Y ;
Kamataki, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 281 (03) :810-814
[4]   Structural characterization of a new variant of the CYP2A6 gene (CYP2A6*1B) apparently diagnosed as heterozygotes of CYP2A6*1A and CYP2A6*4C [J].
Ariyoshi, N ;
Takahashi, Y ;
Miyamoto, M ;
Umetsu, Y ;
Daigo, S ;
Tateishi, T ;
Kobayashi, S ;
Mizorogi, Y ;
Loriot, MA ;
Stücker, I ;
Beaune, P ;
Kinoshita, M ;
Kamataki, T .
PHARMACOGENETICS, 2000, 10 (08) :687-693
[5]   Evidence for endogenous formation of tobacco-specific nitrosamines in rats treated with tobacco alkaloids and sodium nitrite [J].
Carmella, SG ;
Borukhova, A ;
Desai, D ;
Hecht, SS .
CARCINOGENESIS, 1997, 18 (03) :587-592
[6]   A TOBACCO SMOKE-DERIVED NITROSAMINE, 4-(METHYLNITROSAMINO)-1-(3-PYRIDYL)-1-BUTANONE, IS ACTIVATED BY MULTIPLE HUMAN CYTOCHROME P450S INCLUDING THE POLYMORPHIC HUMAN CYTOCHROME P4502D6 [J].
CRESPI, CL ;
PENMAN, BW ;
GELBOIN, HV ;
GONZALEZ, FJ .
CARCINOGENESIS, 1991, 12 (07) :1197-1201
[7]   A novel mutant allele of the CYP2A6 gene (CYP2A6*11) found in a cancer patient who showed poor metabolic phenotype towards tegafur [J].
Daigo, S ;
Takahashi, Y ;
Fujieda, M ;
Ariyoshi, N ;
Yamazaki, H ;
Koizumi, W ;
Tanabe, S ;
Saigenji, K ;
Nagayama, S ;
Ikeda, K ;
Nishioka, Y ;
Kamataki, T .
PHARMACOGENETICS, 2002, 12 (04) :299-306
[8]  
FERNANDEZSALGUERO P, 1995, AM J HUM GENET, V57, P651
[9]  
Fujieda Masaki, 2003, Drug Metab Pharmacokinet, V18, P86, DOI 10.2133/dmpk.18.86
[10]   Predicting the mutagenicity of tobacco-related N-nitrosamines in humans using 11 strains of Salmonella typhimurium YG7108, each coexpressing a form of human cytochrome p450 along with NADPH-cytochrome p450 reductase [J].
Fujita, K ;
Kamataki, T .
ENVIRONMENTAL AND MOLECULAR MUTAGENESIS, 2001, 38 (04) :339-346