Hung H C, Chuang J, Chien Y C, Chern H D, Chiang C P, Kuo Y S, Hildesheim A, Chen C J
Graduate Institute of Public Health, College of Public Health, National Taiwan University, Taipei, Republic of China.
Cancer Epidemiol Biomarkers Prev. 1997 Nov;6(11):901-5.
Both genetic and environmental factors are involved in the development of cancer; some phase I and II enzymes involved in the metabolism of carcinogens are polymorphic in genotypes. This case-control study focused on the interactions between oral cancer risk factors and genetic polymorphisms of cytochrome P-450 (CYP) 2E1 and glutathione S-transferase (GST) M1 and GSTT1. A total of 41 male oral cancer cases was recruited from National Taiwan University Hospital, and 123 healthy controls frequency-matched on ethnicity, sex, and age were recruited from residents living in Taipei City and Taipei County. History of cigarette smoking, alcohol drinking, and betel quid chewing was obtained through a standardized questionnaire interview, and genotypes of CYP2E1, GSTM1, and GSTT1 were determined by PCR. Cigarette smoking, alcohol drinking, and betel quid chewing were significantly associated with the risk of oral cancer in a dose-response relationship. All betel quid chewers smoked cigarettes in both the case and control groups. In the multiple logistic regression analysis, those who had null genotypes of GSTM1 and/or GSTT1 had an increased oral cancer risk compared with those who had non-null genotypes of both GSTM1 and GSTT1, showing a multivariate-adjusted odds ratio (OR) of 4.6 with a 95% confidence interval (CI) of 0.9-23.7 (P = 0.08). The CYP2E1 c1/c2 and c2/c2 genotypes were associated with a significantly increased oral cancer risk compared with the c1/c1 genotype among those who did not chew betel quid (OR, 4.7; 95% CI, 1.1-20.2), but not among betel quid chewers. Habitual alcohol drinking was associated with a significantly increased oral cancer risk, showing an OR of 3.0 (95% CI, 1.1-8.8). These results implied that there are gene-gene and gene-environment interactions in the development of oral cancer.
癌症的发生涉及遗传和环境因素;一些参与致癌物代谢的Ⅰ期和Ⅱ期酶在基因型上具有多态性。这项病例对照研究聚焦于口腔癌危险因素与细胞色素P - 450(CYP)2E1、谷胱甘肽S - 转移酶(GST)M1和GSTT1基因多态性之间的相互作用。从台湾大学医院招募了41例男性口腔癌病例,并从台北市和台北县的居民中招募了123名在种族、性别和年龄上频率匹配的健康对照。通过标准化问卷调查获取吸烟、饮酒和嚼槟榔史,并通过聚合酶链反应(PCR)确定CYP2E1、GSTM1和GSTT1的基因型。吸烟、饮酒和嚼槟榔与口腔癌风险呈显著的剂量反应关系。病例组和对照组中所有嚼槟榔者均吸烟。在多因素逻辑回归分析中,与GSTM1和GSTT1均为非无效基因型者相比,GSTM1和/或GSTT1为无效基因型者患口腔癌的风险增加,多因素调整后的比值比(OR)为4.6,95%置信区间(CI)为0.9 - 23.7(P = 0.08)。在不嚼槟榔者中,与CYP2E1 c1/c1基因型相比,CYP2E1 c1/c2和c2/c2基因型与口腔癌风险显著增加相关(OR,4.7;95% CI,1.1 - 20.2),但在嚼槟榔者中并非如此。习惯性饮酒与口腔癌风险显著增加相关,OR为3.0(95% CI,1.1 - 8.8)。这些结果表明口腔癌发生过程中存在基因 - 基因和基因 - 环境相互作用。