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DNA修复基因XRCC3 Thr241Met多态性与肺癌风险:一项荟萃分析。

DNA repair gene XRCC3 Thr241Met polymorphisms and lung cancer risk: a meta-analysis.

作者信息

Bei Liu, Xiao-Dong Tan, Yu-Fang Gao, Jian-Ping Sun, Zhao-Yu Ying

机构信息

Wuhan university, School of Public Health, Wuhan 430071, China.

Wuhan university, School of Public Health, Wuhan 430071, China.

出版信息

Bull Cancer. 2015 Apr;102(4):332-9. doi: 10.1016/j.bulcan.2015.02.003. Epub 2015 Mar 17.

Abstract

BACKGROUND

The X-ray repair cross-complementing group 3 (XRCC3) is a highly suspected candidate gene for cancer susceptibility, and a large amount studies have examined the association of the rs861539 in XRCC3 (Thr241Met) with lung cancer risk in various populations. However, the results remain inconclusive.

METHODS

The electronic database of PubMed, Medline, Embase and CNKI (China National Knowledge Infrastructure) were searched for case-control studies published up to December 05, 2013. A systematic review and meta-analysis was performed to evaluate the relationship between XRCC3 Thr241Met polymorphism and lung cancer risk. Data were extracted and pooled odds ratio (OR) with its 95% confidence intervals (CI) were calculated.

RESULTS

Total 21 studies, including 6880 lung cancer cases and 8329 controls, were available for meta-analysis. Overall, our results showed that the XRCC3 Thr241Met polymorphism was not associated with risk of lung cancer in all genetic contrast models (P>0.05). Stratified analyses by ethnicity (Asians, Caucasians and mixed population) showed similar results. Additionally, no evidence of publication bias was observed by using the funnel plot.

CONCLUSIONS

There is no clear evidence showing a significant correlation between XRCC3 Thr241Met polymorphism and lung cancer risk in total population and stratified analysis by ethnicity. However, studies assessing the gene-gene interactions should be considered to further estimate this gene variant in lung cancer risk.

摘要

背景

X射线修复交叉互补基因3(XRCC3)是一个备受怀疑的癌症易感性候选基因,大量研究已在不同人群中检测了XRCC3基因中的rs861539(Thr241Met)与肺癌风险的关联。然而,结果仍无定论。

方法

检索了PubMed、Medline、Embase和中国知网(CNKI)的电子数据库,查找截至2013年12月5日发表的病例对照研究。进行了系统评价和荟萃分析,以评估XRCC3基因Thr241Met多态性与肺癌风险之间的关系。提取数据并计算合并比值比(OR)及其95%置信区间(CI)。

结果

共有21项研究(包括6880例肺癌病例和8329例对照)可用于荟萃分析。总体而言,我们的结果显示,在所有遗传对比模型中,XRCC3基因Thr241Met多态性与肺癌风险均无关联(P>0.05)。按种族(亚洲人、白种人和混合人群)进行的分层分析显示了相似的结果。此外,通过漏斗图未观察到发表偏倚的证据。

结论

在总体人群以及按种族进行的分层分析中,没有明确证据表明XRCC3基因Thr241Met多态性与肺癌风险之间存在显著相关性。然而,应考虑开展评估基因-基因相互作用的研究,以进一步评估该基因变异在肺癌风险中的作用。

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