摘要: |
[摘要] 目的 探讨DNA修复基因X线修复交叉互补因子1(XRCC1)主要单核苷酸多态性与前列腺癌易感性的关系。方法 在MEDLINE、EMBASE和OVID数据库上检索文献,收集及提取符合纳入标准的以XRCC1密码子194、280、399多态性与前列腺癌易感性为内容的病例对照研究文献,应用Stata统计软件进行Meta分析,比值比(ORs)及其95%可信区间(95%CI)评价关联强度;应用SPSS软件分析吸烟与前列腺癌关系,OR评价其相对危险度。结果 XRCC1 399 Gln/Gln和XRCC1 280 Arg/His与前列腺癌的发病风险有关(Gln/Gln vs Arg/Arg:OR=1.27,95%CI=1.02~1.59;Arg/His vs Arg/Arg:OR=1.66,95%CI=1.09~2.52),尤其在亚组分析中亚洲人的Gln/Gln明显增加了前列腺癌的发病风险(OR=1.52,95%CI=1.18~1.96);Arg194Trp与前列腺癌的发病风险无明显关联。吸烟是前列腺癌的危险因素(χ2=13.974,P=0.000,OR=1.22)。结论 XRCC1 399 Gln/Gln和280 Arg/His可能与前列腺癌的易感性相关。 |
关键词: 前列腺癌 X线修复交叉互补因子1 基因多态性 Meta分析 |
DOI:10.3969/j.issn.1674-3806.2013.08.10 |
分类号:R 737 |
基金项目: |
|
XRCC1 Arg194Trp, Arg280His, Arg399Gln polymorphisms and prostate cancer risk: a Meta-analysis |
LIU Fei,ZHANG Hai-feng,JIAO Wei,et al.
|
Research Center of Medical Science, the People′s Hospital of Guangxi Zhuang Autonmous Region, Nanning 530021, China
|
Abstract: |
[Abstract] Objective To evaluation the relationship between X-ray repair cross-complementing group 1 (XRCC1) single nucleotide polymorphisms (SNPs) and genetic susceptibility to prostate cancer (Pca) risk.Methods We searched on MEDLINE, EMBASE and OVID, collected and abstracted the case-control studies about XRCC1 codon 194, 280, 399 polymorphisms and genetic susceptibility of Pca; did Meta-analysis by Stata, Odds ratios (ORs) and 95% confidence interval (95%CI) were calculated to evaluate correlation strength; the relation between smoking and Pca was analyzed by SPSS, OR evaluated relative risk of smoking.Results XRCC1 399 Gln/Gln and XRCC1 280 Arg/His were related with risk for Pca (Gln/Gln vs Arg/Arg: OR=1.27, 95%CI=1.02~1.59; Arg/His vs Arg/Arg:OR=1.66, 95%CI=1.09~2.52), especially Asian Gln/Gln obviously increased risk for Pca (OR=1.52, 95%CI=1.18~1.96); Arg194Trp was not related with risk for Pca. Smoking was a risk factor of Pca (χ2=13.974, P=0.000, OR=1.22).Conclusion XRCC1 399 Gln/Gln and XRCC1 280 Arg/His were probably related with genetic susceptibility to Pca. |
Key words: Prostate cancer X-ray repair cross-complementing group 1 Genetic polymorphisms Meta-analysis |