Majumder Mousumi, Sikdar Nilabja, Paul Ranjan Rashmi, Roy Bidyut
Human Genetics Unit, Indian Statistical Institute, Kolkata.
Cancer Epidemiol Biomarkers Prev. 2005 Sep;14(9):2106-12. doi: 10.1158/1055-9965.EPI-05-0108.
An individual's susceptibility to oral precancer and cancer depends not only on tobacco exposure but also on the genotypes/haplotypes at susceptible loci. In this hospital-based case-control study, 310 cancer patients, 197 leukoplakia patients, and 348 controls were studied to determine risk of the disease due to polymorphisms at three sites on XRCC1 and one site on XRCC3. Independently, variant genotypes on these loci did not modulate risk of leukoplakia and cancer except for the XRCC1 (codon 280) risk genotype in exclusive smokeless tobacco users with leukoplakia [odds ratios (OR), 2.4; 95% confidence intervals (CI), 1.0-5.7]. But variant haplotypes, containing one variant allele, on XRCC1 increased the risk of leukoplakia (OR, 1.3; 95% CI, 1.0-1.7). Among stratified samples, mixed tobacco users, carrying variant haplotypes, also had increased risk of both leukoplakia (OR, 2.2; 95% CI, 1.3-3.9) and cancer (OR, 1.9; 95% CI, 1.2-3.1). In a previous study on this population, it was shown that the GSTM3 (A/A) genotype increased the risk of oral leukoplakia and cancer among smokers, which has also been substantiated in this study with expanded sample sizes. The simultaneous presence of two risk genotypes in smokers, one on each of two loci, GSTM3 and XRCC1 (codon 280), increased the risk of cancer (OR, 2.4; 95% CI, 1.0-5.8). Again, smokers carrying two risk genotypes, one on each of two loci, GSTM3 and XRCC1 (codon 399), were also overrepresented in both leukoplakia and cancer populations (P(trend) = 0.02 and 0.04, respectively) but enhancement of risks were not observed; probably due to small sample sizes. Therefore, the presence of variant haplotypes on XRCC1 and two risk genotypes, one on each of two loci, GSTM3 and XRCC1, could be useful to determine the leukoplakias that might progress to cancer in a group of patients.
个体对口腔癌前病变和癌症的易感性不仅取决于烟草暴露情况,还取决于易感基因座处的基因型/单倍型。在这项基于医院的病例对照研究中,对310名癌症患者、197名白斑病患者和348名对照进行了研究,以确定XRCC1基因上三个位点和XRCC3基因上一个位点的多态性导致疾病的风险。单独来看,除了在仅使用无烟烟草的白斑病患者中XRCC1(密码子280)风险基因型外,这些基因座上的变异基因型并未调节白斑病和癌症的风险[比值比(OR)为2.4;95%置信区间(CI)为1.0 - 5.7]。但是,XRCC1上含有一个变异等位基因的变异单倍型增加了白斑病的风险(OR为1.3;95%CI为1.0 - 1.7)。在分层样本中,携带变异单倍型的混合型烟草使用者患白斑病(OR为2.2;95%CI为1.3 - 3.9)和癌症(OR为1.9;9%CI为1.2 - 3.1)的风险也增加。在之前对该人群的一项研究中表明,GSTM3(A/A)基因型增加了吸烟者患口腔白斑病和癌症的风险,本研究通过扩大样本量也证实了这一点。吸烟者中同时存在两个风险基因型,分别位于两个基因座GSTM3和XRCC1(密码子280)上,会增加患癌风险(OR为2.4;95%CI为1.0 - 5.8)。同样,携带两个风险基因型,分别位于两个基因座GSTM3和XRCC1(密码子399)上的吸烟者在白斑病和癌症人群中也占比过高(趋势P值分别为0.02和0.04),但未观察到风险增强;可能是由于样本量较小。因此,XRCC1上变异单倍型以及两个风险基因型(分别位于两个基因座GSTM3和XRCC1上)的存在,可能有助于确定一组患者中可能进展为癌症的白斑病。