Oncotarget

Research Papers:

Association between cyclin D1 (CCND1) G870A polymorphism and gastric cancer risk: a meta-analysis

Yafei Zhang, Xianling Zeng, Hongwei Lu, Hong Ji, Enfa Zhao and Yiming Li _

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Oncotarget. 2016; 7:66109-66118. https://doi.org/10.18632/oncotarget.11848

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Abstract

Yafei Zhang1, Xianling Zeng2, Hongwei Lu1, Hong Ji1, Enfa Zhao3, Yiming Li1

1Department of General Surgery, Second Affiliated Hospital, School of Medicine, Xi’an Jiaotong University, Xi’an, Shaanxi, China

2Department of Obstetrics and Gynecology, First Affiliated Hospital, School of Medicine, Xi'an Jiaotong University, Xi'an, Shaanxi, China

3Department of Ultrasound, Second Affiliated Hospital, School of Medicine, Xi’an Jiaotong University, Xi’an, Shaanxi, China

Correspondence to:

Yiming Li, email: liyimingdoc@163.com

Keywords: gastric cancer, cyclin D1 (CCND1) G870A, polymorphism, meta-analysis

Received: October 30, 2015    Accepted: July 14, 2016    Published: September 06, 2016

ABSTRACT

Published data on the association between cyclin D1 (CCND1) G870A polymorphism and gastric cancer (GC) risk are inconclusive. Thus, we conducted a meta-analysis to evaluate the relationship between CCND1 G870A polymorphism and GC risk. We searched PubMed, EMBASE, Web of science and the Cochrane Library up to June 12, 2015 for relevant studies. Odds ratios (ORs) and 95% confidence intervals (CIs) were used to estimate the strength of associations. Nine studies published from 2003 to 2014, with a total of 1813 cases and 2173 controls, were included in this meta-analysis. The pooled results showed that there was no association between CCND1 G870A polymorphism and GC risk in any genetic model. The subgroup analysis stratified by ethnicity showed an increased breast cancer risk in Caucasian based on heterozygote comparison (GA vs. GG: OR=1.49, 95% CI=1.06-2.10, P=0.02). We found the same association in population based (PB) stratified analyses by Source of controls (AA vs. GG: OR=1.39, 95% CI=1.01-1.93, 0.05). When stratifying by the type, Sex and H. pylori infection in dominant model, Interestingly, we found the opposite result in Male (AA + GA vs. GG: OR=0.5, 95% CI=0.33-0.76, P=0.001), there were no association between CCND1 G870A polymorphism and GC risk in any other subgroup. This meta-analysis suggests that CCND1 G870A polymorphism is a risk factor for susceptibility to GC in Caucasians and in general populations. While, CCND1 G870A polymorphism plays a possible protective effect in GC in Male. Further large scale multicenter epidemiological studies are warranted to confirm this finding.


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