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抵抗素基因多态性rs1862513和rs3745367与癌症风险的关联:一项荟萃分析。

Association between rs1862513 and rs3745367 Genetic Polymorphisms of Resistin and Risk of Cancer: A Meta-Analysis.

作者信息

Hashemi Mohammad, Bahari Gholamreza, Tabasi Farhad, Moazeni-Roodi Abdolkarim, Ghavami Saeid

机构信息

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

出版信息

Asian Pac J Cancer Prev. 2018 Oct 26;19(10):2709-2716. doi: 10.22034/APJCP.2018.19.10.2709.

Abstract

The present study aimed to assess any associations between resistin gene (RETN) polymorphisms and cancer susceptibility by conducting a meta-analysis. A comprehensive literature search was performed with PubMed, Web of Science, Scopus and Google Scholar for relevant studies published before April 2018. For the rs1862513 polymorphism, data from 9 studies covering 1,951 cancer patients and 2,295 healthy controls were included in this meta-analysis. Pooled odds ratios (ORs) with 95% confidence intervals (CIs) were calculated. Our meta-analysis revealed that this RETN polymorphism significantly increased the risk of cancer in codominant (OR=1.23, 95% CI= 1.01-1.50, p=0.04, CG vs CC; and OR=1.25, 95% CI= 1.03-1.53, p=0.03, GG vs CC), dominant (OR=1.19, 95% CI= 1.05-1.35, p=0.006, CG+GG vs CC), and allele (OR=1.14, 95% CI= 1.00-1.30, p=0.04, G vs C) inheritance genetic models. Stratification analysis by cancer type revealed that the rs1862513 variant significantly increased the risk of colorectal and breast cancer, and that cancer overall in Caucasians (OR=1.22, 95% CI= 1.04-1.43, p=0.02, CG+GG vs CC; OR=1.18, 95% CI= 1.04-1.34, p=0.01, G vs C). The data revealed no correlation between the rs3745367 polymorphism and cancer risk. Further well-designed studies with larger sample sizes and different ethnicities are warranted to validate the present findings.

摘要

本研究旨在通过进行一项荟萃分析来评估抵抗素基因(RETN)多态性与癌症易感性之间的任何关联。利用PubMed、Web of Science、Scopus和谷歌学术对2018年4月之前发表的相关研究进行了全面的文献检索。对于rs1862513多态性,本荟萃分析纳入了9项研究的数据,涵盖1951例癌症患者和2295例健康对照。计算了合并比值比(OR)及95%置信区间(CI)。我们的荟萃分析显示,在共显性(OR=1.23,95%CI=1.01-1.50,p=0.04,CG与CC相比;OR=1.25,95%CI=1.03-1.53,p=0.03,GG与CC相比)、显性(OR=1.19,95%CI=1.05-1.35,p=0.006,CG+GG与CC相比)和等位基因(OR=1.14,95%CI=1.00-1.30,p=0.04,G与C相比)遗传模型中,这种RETN多态性显著增加了患癌风险。按癌症类型进行的分层分析显示,rs1862513变异显著增加了结直肠癌和乳腺癌的风险,以及白种人中总体癌症的风险(OR=1.22,95%CI=1.04-1.43,p=0.02,CG+GG与CC相比;OR=1.18,95%CI=1.04-1.34,p=0.01,G与C相比)。数据显示rs3745367多态性与癌症风险之间无相关性。需要进一步开展设计良好、样本量更大且涉及不同种族的研究来验证本研究结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e17/6291049/87c4574d2508/APJCP-19-2709-g001.jpg

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