首页> 外文期刊>Cancer epidemiology, biomarkers and prevention: A publication of the American Association for Cancer Research >Increased risk of oral leukoplakia and cancer among mixed tobacco users carrying XRCC1 variant haplotypes and cancer among smokers carrying two risk genotypes: one on each of two loci, GSTM3 and XRCC1 (Codon 280).
【24h】

Increased risk of oral leukoplakia and cancer among mixed tobacco users carrying XRCC1 variant haplotypes and cancer among smokers carrying two risk genotypes: one on each of two loci, GSTM3 and XRCC1 (Codon 280).

机译:在携带XRCC1变异单倍型的混合烟草使用者中,口腔白斑和癌症的风险增加;在携带两种危险基因型的吸烟者中,癌症的风险增加:GSTM3和XRCC1两个基因座中的每一个(密码子280)。

获取原文
获取原文并翻译 | 示例
           

摘要

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.
机译:一个人对口腔癌和癌的易感性不仅取决于烟草暴露,还取决于易感基因座的基因型/单倍型。在这项基于医院的病例对照研究中,研究了310名癌症患者,197名白斑患者和348名对照,以确定由于XRCC1上三个位点和XRCC3上一个位点多态性引起的疾病风险。独立地,这些基因座上的变异基因型没有调节白斑和癌症的风险,除了具有白斑[odds ratios(OR),2.4;无烟的纯吸烟者]中的XRCC1(密码子280)风险基因型。 95%置信区间(CI),1.0-5.7]。但是,XRCC1上含有一个等位基因的变异单倍型增加了白斑的风险(OR,1.3; 95%CI,1.0-1.7)。在分层样本中,携带变异单倍型的混合烟草使用者也有罹患白斑(OR,2.2; 95%CI,1.3-3.9)和癌症(OR,1.9; 95%CI,1.2-3.1)的风险增加。在先前对该人群的研究中,研究表明,GSTM3(A / A)基因型增加了吸烟者口腔白斑和癌症的风险,该研究在样本量扩大的情况下也得到了证实。吸烟者同时存在两种风险基因型,两个基因座分别为GSTM3和XRCC1(密码子280)之一,增加了罹患癌症的风险(OR,2.4; 95%CI,1.0-5.8)。同样,携带两种风险基因型的吸烟者,在白斑和癌症人群中也过分代表了两种基因型,分别是GSTM3和XRCC1(密码子399)两个基因座(P(趋势)分别为0.02和0.04),但风险并未提高观测到的;可能是由于样本量小。因此,XRCC1上存在变异单倍型和两种风险基因型(两个基因座分别为GSTM3和XRCC1之一)可能有助于确定一组患者可能发展为癌症的白斑。

著录项

相似文献

  • 外文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号