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XRCC1 Arg399Gln 多态性增加中国人群结直肠癌发病风险。

XRCC1 Arg399Gln polymorphism contributes to increased risk of colorectal cancer in Chinese population.

机构信息

Department of General Surgery, Shengjing Hospital of China Medical University, No.36 Sanhao Street, Heping district, Shenyang, 110003, China.

出版信息

Mol Biol Rep. 2013 Jul;40(7):4147-51. doi: 10.1007/s11033-012-2463-5. Epub 2013 May 28.

Abstract

Previous studies investigating the association between X-ray repair cross-complementation group 1 (XRCC1) Arg399Gln polymorphism and colorectal cancer risk in Chinese provided inconsistent findings. To assess the association in Chinese population, a meta-analysis was performed. Eligible studies were searched in Pubmed, Emabse, and China National Knowledge Infrastructure databases. Odds ratios (OR) with the corresponding 95 % confidence intervals (95 %CI) were pooled to assess the association. Seven case-control studies involving a total of 2136 colorectal cancer cases and 3168 controls were finally included in the meta-analysis. Our analysis suggested that the variant genotypes of XRCC1 Arg399Gln were associated with an increased risk of colorectal cancer in Chinese population (Gln vs. Arg: random effect model OR = 1.24, 95 %CI = 1.01-1.52, P = 0.041; GlnGln vs. ArgArg: random effect model OR = 1.52, 95 %CI = 1.07-2.15, P = 0.019; and Recessive model: fixed effect model OR = 1.37, 95 %CI = 1.12-1.67, P = 0.002). There was low risk of publication bias in present meta-analysis. Our meta-analysis provides an evidence for the association between XRCC1 Arg399Gln polymorphism and colorectal cancer risk in Chinese population, and XRCC1 Arg399Gln variant genotypes contribute to increased risk of colorectal cancer in Chinese.

摘要

先前的研究调查了 X 射线修复交叉互补组 1(XRCC1)Arg399Gln 多态性与中国人群结直肠癌风险之间的关联,结果并不一致。为了评估中国人群中的这种关联,进行了一项荟萃分析。在 Pubmed、Emabse 和中国国家知识基础设施数据库中搜索了符合条件的研究。使用相应的 95%置信区间(95%CI)汇总了比值比(OR),以评估相关性。最终纳入了 7 项病例对照研究,共涉及 2136 例结直肠癌病例和 3168 例对照。我们的分析表明,XRCC1 Arg399Gln 变异基因型与中国人群结直肠癌风险增加相关(Gln 对 Arg:随机效应模型 OR = 1.24,95%CI = 1.01-1.52,P = 0.041;GlnGln 对 ArgArg:随机效应模型 OR = 1.52,95%CI = 1.07-2.15,P = 0.019;和隐性模型:固定效应模型 OR = 1.37,95%CI = 1.12-1.67,P = 0.002)。目前的荟萃分析存在发表偏倚的风险较低。我们的荟萃分析为 XRCC1 Arg399Gln 多态性与中国人群结直肠癌风险之间的关联提供了证据,并且 XRCC1 Arg399Gln 变异基因型增加了中国人群结直肠癌的风险。

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