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XRCC1 gene polymorphisms and lung cancer susceptibility: a meta-analysis of 44 case-control studies

机译:XRCC1基因多态性与肺癌易感性:一项44个病例对照研究的荟萃分析

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摘要

X-ray repair cross-complementing group 1 gene (XRCC1) has been implicated in risk for lung cancer. However, the results from different studies remain controversial. In this meta-analysis, we have assessed 44 published case-control studies regarding associations of lung cancer risk with three common polymorphisms, codon 194, codon 280 and codon 399, and -77 T > C in the promoter region of XRCC1. The results in total population showed that the risk for lung cancer was increased among the variant homozygote Trp/Trp of codon 194 polymorphism, compared with the wild type Arg/Arg (OR: 1.19; 95 % CI 1.01-1.39), and the variant genotype CC of -77 T > C polymorphism showed a significantly increased risk of developing lung cancer, compared to wild-type genotype TT (OR: 1.91; 95 % CI 1.24-2.94). However, no associations were found between lung cancer risk and codon 280, codon 399. In the subgroup analyses by ethnicity, the OR for the variant homozygote Trp/Trp of codon 194 was 1.21(95 % CI 1.02-1.43) for Asian. When stratified by source of control, we found a protective effect of codon 194 Arg/Trp genotype (OR: 0.87; 95 % CI 0.77-0.98) and risk effect of codon 399 combined Arg/Gln + Gln/Gln variant genotype (OR: 1.09; 95 % CI 1.01-1.18) for lung cancer on the basis of hospital control. Subgroup analyses by histological types of lung cancer indicated that the heterozygote Arg/Trp in codon 194 could decrease and the combined variant genotype Arg/Gln + Gln/Gln in codon 399 could increase the risk of non-small cell lung cancer (OR: 0.69; 95 % CI 0.57-0.85 and OR: 1.14; 95 % CI 1.04-1.24). In conclusion, this meta-analysis has demonstrated that codon 194, codon 399 and -77 T > C polymorphisms of XRCC1 gene might have contributed to individual susceptibility to lung cancer. To further evaluate effect of XRCC1 polymorphisms, gene-gene interaction and gene-environment interaction on lung cancer risk, a single large sample size study with thousands of subjects is required to get conclusive results.
机译:X射线修复交叉互补的第1组基因(XRCC1)与肺癌风险有关。但是,不同研究的结果仍存在争议。在这项荟萃分析中,我们评估了44篇关于肺癌风险与XRCC1启动子区域中三种常见多态性(194位密码子,280位密码子和399位密码子,-77 T> C)的肺癌风险相关性的病例对照研究。总人群中的结果表明,与野生型Arg / Arg(OR:1.19; 95%CI 1.01-1.39)和变体相比,密码子194多态性的纯合子Trp / Trp变种中患肺癌的风险增加了与野生型TT基因型(OR:1.91; 95%CI 1.24-2.94)相比,-77 T> C多态性的CC型CC基因型显示患肺癌的风险显着增加。但是,在肺癌风险与280号密码子和399号密码子之间未发现关联。在按种族进行的亚组分析中,亚洲人194号密码子纯合子Trp / Trp的OR值为1.21(95%CI 1.02-1.43)。当按控制源进行分层时,我们发现了密码子194 Arg / Trp基因型的保护作用(OR:0.87; 95%CI 0.77-0.98)和399密码子联合Arg / Gln + Gln / Gln变异基因型的风险作用(OR: 1.09; 95%CI 1.01-1.18),基于医院控制。按肺癌的组织学类型进行的亚组分析表明,第194位密码子的杂合子Arg / Trp可能降低,而第399位密码子的变体基因型Arg / Gln + Gln / Gln的组合可能增加非小细胞肺癌的风险(或:0.69 ; 95%CI 0.57-0.85和OR:1.14; 95%CI 1.04-1.24)。总之,这项荟萃分析表明,XRCC1基因的194位密码子,399位密码子和-77 T> C多态性可能导致了个体对肺癌的易感性。为了进一步评估XRCC1多态性,基因-基因相互作用和基因-环境相互作用对肺癌风险的影响,需要对成千上万的受试者进行单个大样本研究以得出结论。

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