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miR-218 rs11134527 多态性与亚洲人群某些类型癌症风险的关联:基于病例对照研究的更新荟萃分析。

Association between miR-218 rs11134527 polymorphism and risk of selected types of cancer in Asian population: An updated meta-analysis of case-control studies.

机构信息

Department of Clinical Biochemistry, Iranshahr University of Medical Sciences, Iranshahr, Iran.

Department of Clinical Biochemistry, School of Medicine, Zahedan University of Medical Sciences, Zahedan, Iran.

出版信息

Gene. 2018 Dec 15;678:370-376. doi: 10.1016/j.gene.2018.08.053. Epub 2018 Aug 16.

Abstract

Several studies inspected the relationship between miR-218 rs11134527 polymorphism and the risk of some human cancers, but the findings remains controversial. We designed an update meta-analysis aiming to validate the association between rs11134527 polymorphism of miR-218 and cancer risk. Eligible studies including 7989 cancer cases and 8761 controls were recognized by searching Web of Science, PubMed, Scopus, and Google scholar databases. Pooled odds ratios (ORs) with 95% confidence intervals (CIs) were estimated to quantitatively evaluate the association between rs11134527 variant and cancer risk. The overall results indicated no significant relationship between miR-218 rs11134527 polymorphism and cancer risk in codominant, dominant, recessive, overdominant, and allele inheritance model tested. Stratified analysis showed that rs11134527 variant significantly increased the risk of developing esophageal squamous cell carcinoma (ESCC) in heterozygous codominant (OR = 1.32, 95%CI = 1.03-1.69, p = 0.03, AG vs GG) inheritance model. In summary, the findings of this meta-analysis did not support an association between miR-218 rs11134527 polymorphism and cancer risk. Stratified analysis showed that rs11134527 variant significantly increased the risk of developing ESCC. Larger and well-designed researches are needed to estimate this association in detail.

摘要

多项研究检验了 miR-218 rs11134527 多态性与某些人类癌症风险之间的关系,但研究结果仍存在争议。我们设计了一项更新的荟萃分析,旨在验证 miR-218 rs11134527 多态性与癌症风险之间的关联。通过搜索 Web of Science、PubMed、Scopus 和 Google scholar 数据库,确定了纳入 7989 例癌症病例和 8761 例对照的合格研究。使用合并优势比(OR)和 95%置信区间(CI)定量评估 rs11134527 变异与癌症风险之间的关系。总体结果表明,在共显性、显性、隐性、超显性和等位基因遗传模型中,miR-218 rs11134527 多态性与癌症风险之间没有显著关系。分层分析显示,rs11134527 变异在杂合子共显性遗传模型(OR = 1.32,95%CI = 1.03-1.69,p = 0.03,AG 与 GG)中显著增加了患食管鳞癌(ESCC)的风险。综上所述,本荟萃分析的结果不支持 miR-218 rs11134527 多态性与癌症风险之间存在关联。分层分析显示,rs11134527 变异显著增加了患 ESCC 的风险。需要更大和精心设计的研究来详细评估这种关联。

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