CYP1A1 and GSTM1 genetic polymorphisms and lung cancer risk in Caucasian non-smokers:: a pooled analysis

被引:144
作者
Hung, RJ
Boffetta, P
Brockmöller, J
Butkiewicz, D
Cascorbi, I
Clapper, ML
Garte, S
Haugen, A
Hirvonen, A
Anttila, S
Kalina, I
Le Marchand, L
London, SJ
Rannug, A
Romkes, M
Salagovic, J
Schoket, B
Gaspari, L
Taioli, E
机构
[1] Int Agcy Res Canc, Unit Environm Canc Epidemiol, F-69372 Lyon 08, France
[2] Univ Calif Los Angeles, Sch Publ Hlth, Dept Epidemiol, Los Angeles, CA 90024 USA
[3] Univ Gottingen, Inst Clin Pharmacol, D-3400 Gottingen, Germany
[4] Ctr Oncol, Dept Tumor Biol, Gliwice, Poland
[5] Ernst Moritz Arndt Univ Greifswald, Inst Pharmacol, D-17487 Greifswald, Germany
[6] Fox Chase Canc Ctr, Div Populat Sci, Philadelphia, PA 19111 USA
[7] Fox Chase Canc Ctr, Div Med Sci, Philadelphia, PA 19111 USA
[8] Genet Res Inst ONLUS, Milan, Italy
[9] Natl Inst Occupat Hlth, Dept Toxicol, Oslo, Norway
[10] Finnish Inst Occupat Hlth, Helsinki, Finland
[11] Safarik Univ, Sch Med, Dept Med Biol, Kosice, Slovakia
[12] Univ Hawaii, Canc Res Ctr Hawaii, Honolulu, HI 96813 USA
[13] NIEHS, Epidemiol Branch, Res Triangle Pk, NC 27709 USA
[14] Karolinska Inst, Inst Environm Med, S-10401 Stockholm, Sweden
[15] Univ Pittsburgh, Ctr Clin Pharmacol, Pittsburgh, PA USA
[16] Natl Inst Environm Hlth, Dept Biochem, Budapest, Hungary
[17] Univ Milan, IRCCS, Dept Environm Med, Milan, Italy
关键词
D O I
10.1093/carcin/bgg026
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Polymorphisms for genes encoding the metabolic enzymes cytochrome P450 1A1 (CYP1A1) and glutathione S-transferase M1 (GSTM1) might contribute to the variability in individual susceptibility to lung cancer. The role of CYP1A1 and GSTM1 in lung carcinogenesis might be more important at low levels of exposure to carcinogens. Non-smokers represent a population at low exposure, however, they are often overlooked because of the small number of cases. We therefore conducted a pooled analysis of 14 case-control studies on lung cancer in Caucasian non-smokers with comparable information on genetic polymorphisms included in the International Collaborative Study on Genetic Susceptibility to Environmental Carcinogens. We pooled the raw data from a total of 302 cases and 1631 controls with random effects models. We also evaluated the possibility of inclusion bias and conducted influence analyses. The odds ratio (OR) of lung cancer for the variant CYP1A1 Ile(462)Val polymorphism (Ile/Val, Val/Val) was 2.99 [95% confidence interval (95%CI) 1.51-5.91]; this effect was stronger on lung adenocarcinoma (OR 4.85, 95%CI 2.03-11.6). After excluding outlying or imprecise studies, we did not observe a significant effect of the CYP1A1 MspI ((TC)-C-3801) polymorphism or GSTM1 null genotype (OR 1.20, 95%CI 0.89-1.63). Furthermore, our analyses suggested a combined effect of the CYP1A1 Ile(462)Val polymorphism and GSTM1 null genotype. The OR for the combination of the CYP1A1 Ile(462)Val variant and GSTM1 null genotype was 4.67 (95%CI 2.00-10.9) compared with the concurrent presence of the CYP1A1 wild-type and GSTM1 non-null genotype. We did not observe a modification of the effect of the GSTM1 null genotype according to exposure to environmental tobacco smoke and urban/rural residence. Our study therefore suggests that the CYP1A1 Ile(462)Val variant allele might play a role in lung carcinogenesis among non-smokers, possibly in combination with the GSTM1 null genotype.
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页码:875 / 882
页数:8
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