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DNA修复基因XRCC1 Arg194Trp多态性与肝细胞癌易感性:一项荟萃分析。

DNA repair gene XRCC1 Arg194Trp polymorphism and susceptibility to hepatocellular carcinoma: A meta-analysis.

作者信息

Li Wenyan, Yang Feng, Gui Yongxian, Bian Junjie

机构信息

Department of Oncology, Xinxiang Central Hospital, Xinxiang Medical College, Xinxiang, Henan 453000, P.R. China.

Department of Integrated Medicine, Henan Cancer Hospital, Zhengzhou, Henan 450000, P.R. China.

出版信息

Oncol Lett. 2014 Oct;8(4):1725-1730. doi: 10.3892/ol.2014.2351. Epub 2014 Jul 15.

Abstract

The arginine194tryptophan (Arg194Trp) polymorphism in the X-ray repair cross-complementing group 1 (XRCC1) gene has been reported to be associated with hepatocellular carcinoma (HCC), however, the results from previous studies are conflicting. The present study aimed to investigate the association between the XRCC1 Arg194Trp polymorphism and the risk of HCC, using a meta-analysis of previously published studies. PubMed (http://www.ncbi.nlm.nih.gov/pubmed/), Google Scholar (http://scholar.google.co.uk/) and the China National Knowledge Infrastructure databases (http://www.cnki.net/) were systematically searched to identify relevant studies published prior to October 2013. A meta-analysis was performed to examine the association between the Arg194Trp gene polymorphism and the susceptibility to HCC. Odds ratios (ORs) and 95% confidence intervals (95% CIs) were calculated. The meta-analysis consisted of six case-control studies that included 1,451 HCC cases and 1,398 healthy controls. Meta-analysis results based on all the studies showed no significant association between the XRCC1 Arg194Trp gene polymorphism and the risk of HCC (Trp/Trp vs. Arg/Arg: OR, 1.17; 95% CI, 0.89-1.55; Trp/Trp vs. Arg/Trp: OR, 0.94; 95% CI, 0.59-1.51; dominant model: OR, 0.97; 95% CI, 0.63-1.49; recessive model: OR, 1.22; 95% CI, 0.89-1.67). In the subgroup analysis, three studies with sample sizes of >300 produced similar results that indicated that the Arg194Trp gene polymorphism had no association with an increased or decreased risk of HCC. The pooled ORs were not markedly different following the exclusion of two studies deviating from the Hardy-Weinberg equilibrium in the control group, which indicated the reliability of the meta-analysis results. In conclusion, the XRCC1 Arg194Trp polymorphism may not be a risk or protective factor for HCC. Further large and well-designed studies are required to confirm these results.

摘要

据报道,X射线修复交叉互补基因1(XRCC1)中的精氨酸194色氨酸(Arg194Trp)多态性与肝细胞癌(HCC)相关,然而,先前研究的结果相互矛盾。本研究旨在通过对先前发表的研究进行荟萃分析,探讨XRCC1 Arg194Trp多态性与HCC风险之间的关联。系统检索了PubMed(http://www.ncbi.nlm.nih.gov/pubmed/)、谷歌学术(http://scholar.google.co.uk/)和中国知网数据库(http://www.cnki.net/),以识别2013年10月之前发表的相关研究。进行荟萃分析以检验Arg194Trp基因多态性与HCC易感性之间的关联。计算比值比(OR)和95%置信区间(95%CI)。荟萃分析包括六项病例对照研究,共纳入1451例HCC病例和1398例健康对照。基于所有研究的荟萃分析结果显示,XRCC1 Arg194Trp基因多态性与HCC风险之间无显著关联(Trp/Trp与Arg/Arg:OR,1.17;95%CI,0.89 - 1.55;Trp/Trp与Arg/Trp:OR,0.94;95%CI,0.59 - 1.51;显性模型:OR,0.97;95%CI,0.63 - 1.49;隐性模型:OR,1.22;95%CI,0.89 - 1.67)。在亚组分析中,三项样本量>300的研究得出了相似的结果,表明Arg194Trp基因多态性与HCC风险的增加或降低无关。排除两项对照组偏离哈迪 - 温伯格平衡的研究后,合并的OR没有明显差异,这表明荟萃分析结果的可靠性。总之,XRCC1 Arg194Trp多态性可能不是HCC的风险或保护因素。需要进一步开展大规模且设计良好的研究来证实这些结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d857/4156170/1bf817b51e84/OL-08-04-1725-g00.jpg

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