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人微小RNA-499 rs3746444多态性与癌症风险:一项荟萃分析

Hsa-mir-499 rs3746444 polymorphism and cancer risk: a meta-analysis.

作者信息

Zou Peng, Zhao Lin, Xu Haitao, Chen Ping, Gu Aihua, Liu Ning, Zhao Peng, Lu Ailin

机构信息

Department of Neurosurgery, the First Affiliated Hospital, Nanjing Medical University, Nanjing, Jiangsu 210029, China;

出版信息

J Biomed Res. 2012 Jul;26(4):253-9. doi: 10.7555/JBR.26.20110122. Epub 2012 Apr 16.

DOI:10.7555/JBR.26.20110122
PMID:23554757
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3596741/
Abstract

MicroRNAs (miRNAs) are gene regulators involved in numerous diseases including cancer, heart disease, neurological disorders, vascular abnormalities and autoimmune conditions. Although hsa-mir-499 rs3746444 polymorphism was shown to contribute to the susceptibility of multiple genes to cancer, the data have yielded conflicting results. Therefore, this meta-analysis was performed to provide a comprehensive assessment of potential association between hsa-mir-499 rs3746444 polymorphism and cancer risk. In this meta-analysis, a total of 9 articles regarding 10 eligible case-control studies in English (including 6134 cases and 7141 controls) were analyzed. No significant association between hsa-mir-499 rs3746444 polymorphism and overall cancer risk was demonstrated. However, an increased risk was observed in the subgroup of breast cancer patients (G allele vs A allele: OR = 1.10, 95% CI = 1.00-1.20; P heterogeneity = 0.114; I (2) = 53.9%) and population-based studies (G allele vs A allele: OR = 1.12, 95% CI = 1.00-1.25; P heterogeneity = 0.062; I (2) = 64.0%). The findings suggested an association between hsa-mir-499 rs3746444 polymorphism and increased risk to breast cancer.

摘要

微小RNA(miRNA)是参与多种疾病的基因调节因子,这些疾病包括癌症、心脏病、神经紊乱、血管异常和自身免疫性疾病。尽管已表明人微小RNA-499(hsa-mir-499)rs3746444多态性与多种基因对癌症的易感性有关,但数据结果相互矛盾。因此,进行了这项荟萃分析,以全面评估hsa-mir-499 rs3746444多态性与癌症风险之间的潜在关联。在这项荟萃分析中,共分析了9篇英文文章,涉及10项符合条件的病例对照研究(包括6134例病例和7141例对照)。未证明hsa-mir-499 rs3746444多态性与总体癌症风险之间存在显著关联。然而,在乳腺癌患者亚组(G等位基因与A等位基因:比值比=1.10,95%置信区间=1.00-1.20;异质性P=0.114;I²=53.9%)和基于人群的研究(G等位基因与A等位基因:比值比=1.12,95%置信区间=1.00-1.25;异质性P=0.062;I²=64.0%)中观察到风险增加。这些发现表明hsa-mir-499 rs3746444多态性与乳腺癌风险增加之间存在关联。

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