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在白种人群中,BRCC5基因多态性与卵巢癌风险增加相关。

An increased risk of ovarian cancer associated with polymorphism in BRCC5 gene in Caucasian populations.

作者信息

Liang Hua, Li Yan, Luo Ruo-Yu, Shen Fu-Jin

机构信息

Renmin Hospital, Department of Obstetrics & Gynecology, Wuhan University, Wuhan, 430060, People's Republic of China.

出版信息

Tumour Biol. 2014 Sep;35(9):9179-84. doi: 10.1007/s13277-014-2135-2. Epub 2014 Jun 14.

Abstract

Several reports on the association between the BRCC5 gene polymorphism and ovarian cancer risk have been published recently, but the estimates of the risk vary widely. We thus performed a meta-analysis in an effort to determine the association. To identify the eligible studies, we searched the PubMed, Embase, and CNKI databases, and reviewed all original studies retrieved as well as their citations. The risk of ovarian cancer was estimated using odds ratio (OR) and its 95 % confidence interval (CI). Meta-analysis of seven comparisons revealed an obvious rise in the risk of ovarian cancer under the CC vs. GG contrast model (OR = 1.52, 95 % CI = 1.07-2.16, P OR = 0.020). A similar increase was also indicated in the CC vs. GC + GG model (OR = 2.10, 95 % CI = 1.51-2.93, P OR < 0.001). Our meta-analysis indicates that the BRCC5 polymorphism may be a candidate modifier of ovarian cancer risk in Caucasians.

摘要

最近发表了几篇关于BRCC5基因多态性与卵巢癌风险之间关联的报告,但风险估计差异很大。因此,我们进行了一项荟萃分析以确定这种关联。为了确定符合条件的研究,我们检索了PubMed、Embase和CNKI数据库,并查阅了检索到的所有原始研究及其参考文献。使用比值比(OR)及其95%置信区间(CI)来估计卵巢癌风险。对七项比较的荟萃分析显示,在CC与GG对比模型下,卵巢癌风险明显升高(OR = 1.52,95% CI = 1.07 - 2.16,P OR = 0.020)。在CC与GC + GG模型中也显示出类似的升高(OR = 2.10,95% CI = 1.51 - 2.93,P OR < 0.001)。我们的荟萃分析表明,BRCC5基因多态性可能是白种人卵巢癌风险的一个候选修饰因素。

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