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两种常见多态性(miR-146a rs2910164和miR-196a2 rs11614913)与胃癌易感性之间的关联:一项荟萃分析。

The association between two common polymorphisms (miR-146a rs2910164 and miR-196a2 rs11614913) and susceptibility to gastric cancer: A meta-analysis.

作者信息

Wei Yuanxiu, Li Li, Gao Jian

出版信息

Cancer Biomark. 2015;15(3):235-48. doi: 10.3233/CBM-150470.

Abstract

BACKGROUND

Accumulating evidence has demonstrated that single nucleotide polymorphisms (SNPs) in microRNAs (miR-146a rs2910164 and miR-196a2 rs11614913) might be connected with the risk of gastric cancer (GC). However, the studies are controversial and inconclusive. We performed this meta-analysis to assess the potential association between two SNPs and susceptibility to GC systematically and comprehensively.

METHODS

Through a systematic literature search, eight case-control studies for rs2910164 and seven case-control studies for rs11614913 were identified and included in this meta-analysis. The odds ratios (ORs) and 95% confidence intervals (95% CIs) were calculated to investigate the association between the two SNPs and the GC risk. Additionally, a subgroup analysis and a publication bias test were performed.

RESULTS

Our results showed that the only significant association between the miR-146a rs2910164 polymorphism and susceptibility to gastric cancer was found in the heterozygous model (OR = 0.884, 95% CI: 0.795-0.983, Ph= 0.326, P = 0.022). Similarly, when stratified by ethnicity, there was an obvious correlation in the heterozygous model (OR = 0.734, 95% CI: 0.542-0.993, Ph = 0.441, P = 0.045) in Caucasians but not in Asians. For miR-196a2, this meta-analysis suggested that neither the allele frequency nor the genotype distribution of the polymorphism was associated with GC risk in the five genetic models. Similarly, the subgroup analysis by ethnicity showed no association with susceptibility to GC.

CONCLUSION

Our studies suggested that the miR-146a rs2910164 polymorphism might marginally contribute to a decreased risk of gastric cancer, especially in Caucasians, whereas the miR-196a2 rs11614913 polymorphism might not be associated with susceptibility to GC.

摘要

背景

越来越多的证据表明,微小RNA中的单核苷酸多态性(SNP,即miR-146a rs2910164和miR-196a2 rs11614913)可能与胃癌(GC)风险相关。然而,这些研究存在争议且尚无定论。我们进行了这项荟萃分析,以系统全面地评估这两个SNP与GC易感性之间的潜在关联。

方法

通过系统的文献检索,确定了8项关于rs2910164的病例对照研究和7项关于rs11614913的病例对照研究,并纳入本荟萃分析。计算比值比(OR)和95%置信区间(95%CI),以研究这两个SNP与GC风险之间的关联。此外,还进行了亚组分析和发表偏倚检验。

结果

我们的结果显示,仅在杂合子模型中发现miR-146a rs2910164多态性与胃癌易感性之间存在显著关联(OR = 0.884,95%CI:0.795 - 0.983,Ph = 0.326,P = 0.022)。同样,按种族分层时,在白种人的杂合子模型中存在明显相关性(OR = 0.734,95%CI:0.542 - 0.993,Ph = 0.441,P = 0.045),而在亚洲人中则无相关性。对于miR-196a2,本荟萃分析表明,在五种遗传模型中,该多态性的等位基因频率和基因型分布均与GC风险无关。同样,按种族进行的亚组分析显示与GC易感性无关联。

结论

我们的研究表明,miR-146a rs2910164多态性可能对降低胃癌风险有一定作用,尤其是在白种人中,而miR-196a2 rs11614913多态性可能与GC易感性无关。

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