Vineis Paolo, Veglia Fabrizio, Anttila Sisko, Benhamou Simone, Clapper Margie L, Dolzan Vita, Ryberg David, Hirvonen Ari, Kremers Pierre, Le Marchand Loic, Pastorelli Roberta, Rannug Agneta, Romkes Marjorie, Schoket Bernadette, Strange Richard C, Garte Seymour, Taioli Emanuela
Imperial College London, London, UK.
Biomarkers. 2004 May-Jun;9(3):298-305. doi: 10.1080/13547500400011070.
Gene-environment interactions have been extensively studied in lung cancer. It is likely that several genetic polymorphisms cooperate in increasing the individual risk. Therefore, the study of gene-gene interactions might be important to identify high-susceptibility subgroups. GSEC is an initiative aimed at collecting available data sets on metabolic polymorphisms and the risks of cancer at several sites and performing pooled analyses of the original data. Authors of published papers have provided original data sets. The present paper refers to gene-gene interactions in lung cancer and considers three polymorphisms in three metabolic genes: CYP1A1, GSTM1 and GSTT1. The present analyses compare the gene gene interactions of the CYP1A12A, GSTM1 and GSTT1 polymorphisms from studies on lung cancer conducted in Europe and the USA between 1991 and 2000. Only Caucasians have been included. The data set includes 1466 cases and 1488 controls. The only clear-cut association was found with CYP1A12A. This association remained unchanged after stratification by polymorphisms in other genes (with an odds ratio [OR] of approximately 2.5), except when interaction with GSTM1 was considered. When the OR for CYP1A12A was stratified according to the GSTM1 genotype, the OR was increased only among the subjects who had the null (homozygous deletion) GSTM1 genotype (OR = 2.8, 95% CI = 0.9-8.4). The odds ratio for the interactive term (CYP1A12A by GSTM1) in logistic regression was 2.7 (95% CI = 0.5-15.3). An association between lung cancer and the homozygous CYP1A1*2A genotype is confirmed. An apparent and biologically plausible interaction is suggested between this genotype and GSTM1.
基因-环境相互作用在肺癌研究中已得到广泛探讨。很可能有几种基因多态性共同作用增加个体患病风险。因此,研究基因-基因相互作用对于识别高易感性亚组可能很重要。基因-环境与癌症易感性协作组(GSEC)是一项旨在收集有关代谢多态性和多个部位癌症风险的现有数据集,并对原始数据进行汇总分析的倡议。已发表论文的作者提供了原始数据集。本文探讨肺癌中的基因-基因相互作用,并研究三个代谢基因(CYP1A1、GSTM1和GSTT1)中的三种多态性。本分析比较了1991年至2000年在欧洲和美国进行的肺癌研究中CYP1A12A、GSTM1和GSTT1多态性的基因-基因相互作用。仅纳入了白种人。数据集包括1466例病例和1488例对照。唯一明确的关联是与CYP1A12A相关。在按其他基因的多态性分层后,这种关联保持不变(优势比[OR]约为2.5),但在考虑与GSTM1的相互作用时除外。当根据GSTM1基因型对CYP1A12A的OR进行分层时,仅在具有GSTM1无效(纯合缺失)基因型的受试者中OR增加(OR = 2.8,95%置信区间 = 0.9 - 8.4)。逻辑回归中交互项(CYP1A12A与GSTM1)的优势比为2.7(95%置信区间 = 0.5 - 15.3)。肺癌与纯合CYP1A1*2A基因型之间的关联得到证实。该基因型与GSTM1之间存在明显且生物学上合理的相互作用。