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MiR-146a基因变异与消化系统癌症风险的关系:一项荟萃分析

A genetic variant in MiR-146a modifies digestive system cancer risk: a meta-analysis.

作者信息

Li Ying-Jun, Zhang Zhen-Yu, Mao Ying-Ying, Jin Ming-Juan, Jing Fang-Yuan, Ye Zhen-Hua, Chen Kun

机构信息

Department of Epidemiology and Biostatistics, Zhejiang University School of Public Health, Hangzhou, China E-mail :

出版信息

Asian Pac J Cancer Prev. 2014;15(1):145-50. doi: 10.7314/apjcp.2014.15.1.145.

Abstract

MicroRNAs (miRNAs) negatively regulate gene expression and act as tumor suppressors or oncogenes in oncogenesis. The association between a single nucleotide polymorphism (SNP) in miR-146a rs2910164 and susceptibility to digestive system cancers was inconsistent in previous studies. In this study, we conducted a literature search of PubMed to identify all relevant studies published before August 31, 2013. A total of 21 independent case-control studies were included in this updated meta-analysis with 9,558 cases and 10,614 controls. We found that the miR-146a rs2910164 polymorphism was significantly associated with decreased risk of digestive system cancers in an allele model (OR=0.90, 95%CI 0.87-0.94), homozygote model (OR=0.84, 95%CI 0.77-0.91), dominant model (OR=0.90, 95%CI 0.84-0.96), and recessive model (OR=0.85, 95%CI 0.79-0.91), while in a heterozygous model (OR = 0.99, 95% CI 0.89-1.11) the association showed marginal significance. Subgroup analysis by cancer site revealed decreased risk in colorectal cancer above allele model (OR=0.90, 95%CI 0.83- 0.97) and homozygote model (OR=0.85, 95%CI 0.72-1.00). Similarly, decreased cancer risk was observed when compared with allele model (OR=0.87, 95%CI 0.81-0.93) and recessive model (OR=0.81, 95%CI 0.72-0.90) in gastric cancer. When stratified by ethnicity, genotyping methods and quality score, decreased cancer risks were also observed. This current meta-analysis indicated that miR-146a rs2910164 polymorphism may decrease the susceptibility to digestive system cancers, especially in Asian populations.

摘要

微小RNA(miRNA)通过负向调控基因表达,在肿瘤发生过程中发挥肿瘤抑制因子或癌基因的作用。以往研究中,miR-146a rs2910164单核苷酸多态性(SNP)与消化系统癌症易感性之间的关联并不一致。在本研究中,我们检索了PubMed数据库,以查找2013年8月31日前发表的所有相关研究。本项更新的荟萃分析共纳入21项独立的病例对照研究,包括9558例病例和10614例对照。我们发现,在等位基因模型(OR=0.90,95%CI 0.87 - 0.94)、纯合子模型(OR=0.84,95%CI 0.77 - 0.91)、显性模型(OR=0.90,95%CI 0.84 - 0.96)和隐性模型(OR=0.85,95%CI 0.79 - 0.91)中,miR-146a rs2910164多态性与消化系统癌症风险降低显著相关,而在杂合子模型(OR = 0.99,95%CI 0.89 - 1.11)中,该关联显示出边际显著性。按癌症部位进行的亚组分析显示,在等位基因模型(OR=0.90,95%CI 0.83 - 0.97)和纯合子模型(OR=0.85,95%CI 0.72 - 1.00)中,结直肠癌风险降低。同样,在胃癌中,与等位基因模型(OR=0.87,95%CI 0.81 - 0.93)和隐性模型(OR=0.81,95%CI 0.72 - 0.90)相比,癌症风险也降低。按种族、基因分型方法和质量评分进行分层时,也观察到癌症风险降低。当前的这项荟萃分析表明,miR-146a rs2910164多态性可能会降低消化系统癌症的易感性,尤其是在亚洲人群中。

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