BACKGROUND/AIMS:MicroRNAs post-transcriptionally regulate the expression of their target genes and their function in a wide range of physiological pathways. Aberrant expression of microRNAs has been implicated in the development of human malignant tumors. Recent reports showed that two single nucleotide polymorphisms (SNPs), miR-146a rs2910164 and miR-196a2 rs11614913, are associated with increased risk of human gastric cancer. Nevertheless, results from the published reports are still inconsistent and inconclusive. Thus, we conducted this meta-analysis study to further evaluate the effects of these two SNPs on susceptibility to human gastric cancer. MATERIALS AND METHODS:Using specific inclusion and exclusion criteria, we extracted data from selected studies that were identified from electronic databases, such as PubMed, Embase, and Wanfang. Odds ratio (ORs) and 95% CIs were then obtained to determine the impact of the two SNPs on susceptibility to human gastric cancer using the statistical software Stata. RESULTS:We identified six studies on rs2910164 and five reports regarding rs11614913 for our meta-analysis. Our data demonstrated that the two SNPs rs2910164 and rs11614913 do not produce any effects on the risk of human gastric cancer under all genetic models. CONCLUSION:There is no significant association between rs2910164 and rs11614913 and the risk of human gastric cancer. However, future studies with large and homogeneous population of patients with gastric cancer and well-matched controls are needed to validate these findings.

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背景/目的:MicroRNA在多种生理途径中转录后调控其靶基因的表达及其功能。 microRNA的异常表达与人类恶性肿瘤的发展有关。最近的报告显示,两个单核苷酸多态性(SNP)miR-146a rs2910164和miR-196a2 rs11614913与人类胃癌的风险增加相关。但是,已发布报告的结果仍然不一致且无定论。因此,我们进行了这项荟萃分析研究,以进一步评估这两个SNP对人胃癌易感性的影响。
材料与方法:使用特定的纳入和排除标准,我们从选定的研究中提取数据,这些研究是从电子数据库(例如PubMed,Embase和Wanfang)中鉴定出来的。然后使用统计软件Stata获得比值比(OR)和95%CI,以确定这两个SNP对人胃癌易感性的影响。
结果:我们对rs2910164进行了六项研究,并针对rs11614913进行了五篇报告,用于我们的荟萃分析。我们的数据表明,在所有遗传模型下,两个SNP rs2910164和rs11614913均不会对人胃癌的风险产生任何影响。
结论:rs2910164和rs11614913与人类胃癌的风险之间没有显着相关性。但是,需要对大量且均质的胃癌患者和匹配良好的对照进行进一步的研究,以验证这些发现。

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