Anantharaman Devasena, Chaubal Pranay M, Kannan Sadhana, Bhisey Rajani A, Mahimkar Manoj B
Cancer Research Institute, Advanced Center for Treatment, Research and Education in Cancer, Tata Memorial Center, Kharghar, Navi Mumbai 410 208, India.
Carcinogenesis. 2007 Jul;28(7):1455-62. doi: 10.1093/carcin/bgm038. Epub 2007 Feb 16.
Oral cancer is the leading cancer type among Southeast Asian men and is causally associated with the use of tobacco. Genetic polymorphisms in xenobiotic-metabolizing enzymes modify the effect of environmental exposures, thereby playing a significant role in gene-environment interactions and hence contribute to the high degree of variance in individual susceptibility to cancer risk. This study investigates the role of polymorphisms at CYP1A1, GSTM1 and GSTT1 to oral squamous cell carcinoma (OSCC) in a case-control study involving 155 patients with precancerous lesions, 458 cancer patients and 729 age and habit-matched controls. Genotypes at these loci were determined by polymerase chain reaction (PCR) and PCR-restriction fragment length polymorphism performed on genomic DNA extracted from peripheral blood lymphocytes. Risk to oral cancer was estimated among different tobacco exposure groups and doses using logistic regression analysis. GSTM1 null genotype conferred 1.29-fold increased risk [95% confidence interval (CI), 1.04-1.65] to OSCC. GSTT1 null genotype, however, conferred 0.57 times reduced risk to OSCC (95% CI, 0.39-0.83), specifically among tobacco chewers (odds ratio 0.27; 95% CI, 0.14-0.53). This risk was further reduced to 0.13 times (95% CI, 0.04-0.46) with increase in lifetime exposure to tobacco. We also investigated risk conferred by these genotypes at two different intra-oral sites, buccal mucosa and tongue. We found increased susceptibility to buccal mucosa cancer among individuals carrying these genetic markers. These results support the finding that GSTM1 null genotype is a risk factor to OSCC among Indian tobacco habits; GSTT1 null genotype, however, emerged as a protective factor.
口腔癌是东南亚男性中最主要的癌症类型,与烟草使用存在因果关联。外源性代谢酶的基因多态性会改变环境暴露的影响,从而在基因-环境相互作用中发挥重要作用,进而导致个体对癌症风险的易感性存在高度差异。本研究在一项病例对照研究中,调查了细胞色素P450 1A1(CYP1A1)、谷胱甘肽S-转移酶M1(GSTM1)和谷胱甘肽S-转移酶T1(GSTT1)基因多态性在口腔鳞状细胞癌(OSCC)中的作用,该研究纳入了155例癌前病变患者、458例癌症患者以及729名年龄和习惯相匹配的对照。通过聚合酶链反应(PCR)以及对从外周血淋巴细胞中提取的基因组DNA进行PCR-限制性片段长度多态性分析来确定这些位点的基因型。使用逻辑回归分析评估不同烟草暴露组和剂量下患口腔癌的风险。GSTM1基因缺失型使患OSCC的风险增加1.29倍[95%置信区间(CI),1.04 - 1.65]。然而,GSTT1基因缺失型使患OSCC的风险降低0.57倍(95% CI,0.39 - 0.83),特别是在嚼烟者中(比值比0.27;95% CI,0.14 - 0.53)。随着终生烟草暴露量增加,这种风险进一步降至0.13倍(95% CI,0.04 - 0.46)。我们还研究了这些基因型在口腔内两个不同部位,即颊黏膜和舌部所带来的风险。我们发现携带这些基因标记物的个体对颊黏膜癌的易感性增加。这些结果支持了以下发现:在印度人的烟草使用习惯中,GSTM1基因缺失型是患OSCC的一个风险因素;然而,GSTT1基因缺失型则是一个保护因素。