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DNMT3B基因-149C>T多态性与结直肠癌风险无关:基于病例对照研究的Meta分析证据

The -149C>T polymorphism of DNMT3B is not associated with colorectal cancer risk: Evidence from a meta-analysis based on case-control studies.

作者信息

Fang Chunyan, Sun Wenqi, Han Huirong, Shi Lihong, Wang Lin, Zhao Yan, Tan Yang

机构信息

Laboratory of Applied Pharmacology, Weifang Medical University, Weifang 261042;

出版信息

Exp Ther Med. 2012 Oct;4(4):728-732. doi: 10.3892/etm.2012.638. Epub 2012 Jul 17.

Abstract

The aim of this study was to examine the association between the -149C>T polymorphism of DNA methyltransferase 3B (DNMT3B) and colorectal cancer (CRC) susceptibility. A comprehensive search was conducted to identify all case-control studies of the -149C>T polymorphism of DNMT3B and CRC risk. Statistical analysis was performed with the software program Stata (version 12.0) and Review Manager (version 5.0). A total of seven eligible studies, including 2,666 cases and 4,022 controls, associating the DNMT3B polymorphism of -149C>T with the risk of CRC were identified. These studies suggested no significant associations between the -149C>T polymorphism of the DNMT3B gene and the risk of developing CRC in the recessive, dominant and co-dominant models [for CC vs. TT: odds ratio (OR), 0.90; 95% confidence interval (CI), 0.90-1.25; P=0.37; for the recessive model: OR, 0.54, 95% CI, 0.28-1.04; P<0.00001; for the dominant model: OR, 1.07; 95% CI, 0.93-1.23; P=0.83 and C allele vs. T allele: OR, 0.70; 95% CI, 0.43-1.13; P<0.00001]. In the subgroup analysis, no significant associations were found in the European populations (for CC vs. TT: OR, 1.09; 95% CI, 0.92-1.30; P=0.88; for the recessive model: OR, 1.00; 95% CI, 0.88-1.13; P=0.14; for the dominant model: OR, 1.50; 95% CI, 0.89-2.54; P<0.00001 and C allele vs. T allele: OR, 0.70; 95% CI, 0.38-1.28; P<0.00001). No significant association was found between the -149C>T polymorphism in DNMT3B and CRC susceptibility.

摘要

本研究旨在探讨DNA甲基转移酶3B(DNMT3B)基因-149C>T多态性与结直肠癌(CRC)易感性之间的关联。通过全面检索,以确定所有关于DNMT3B基因-149C>T多态性与CRC风险的病例对照研究。使用Stata软件程序(版本12.0)和Review Manager软件(版本5.0)进行统计分析。共纳入7项符合条件的研究,包括2666例病例和4022例对照,这些研究将DNMT3B基因的-149C>T多态性与CRC风险相关联。这些研究表明,在隐性、显性和共显性模型中,DNMT3B基因的-149C>T多态性与患CRC的风险之间无显著关联[CC与TT比较:比值比(OR)为0.90;95%置信区间(CI)为0.90 - 1.25;P = 0.37;隐性模型:OR为0.54,95% CI为0.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c68/3501434/9c06a32f1530/ETM-04-04-0728-g00.jpg

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