Background: In recent years, numerous studies have been performed to investigate the CCND1 G870Agene polymorphism impact on brain tumors susceptibility. Unfortunately, the results of previous studies wereinconsistent. Therefore, we performed a meta-analysis to derive a more precise estimation of any association.Materials and Methods: We conducted a search in PubMed, Embase and CNKI covering all published papersup to November, 2013. Odds ratios (ORs) and their 95% confidence intervals (95%CIs) were applied to assessassociations. Results: A total of 6 publications including 9 case-control studies met the inclusion criteria. Thepooled ORs for the total included studies showed significant association among comparison A vs G (OR= 1.246,95%CI= 1.092-1.423, p= 0.001), homozygote comparison AA vs GG (OR= 1.566, 95%CI= 1.194-2.054, p= 0.001),heterozygote comparison AG vs GG (OR= 1.290, 95%CI= 0.934-1.782, p= 0.122), dominant model AA/GA vsGG (OR= 1.381, 95%CI= 1.048-1.821, p= 0.022) and recessive model AA vs GA/GG (OR= 1.323, 95%CI= 1.057-1.657, p= 0.015) especially in glioma. Conclusions: CCND1 G870A polymorphism may increase brain tumorrisk, especially for gliomas. However, more primary large scale and well-designed studies are still required toevaluate the interaction of CCND1 G870A polymorphism with brain tumor risk.
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