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Meta-Analysis
. 2014 May;35(5):4977-82.
doi: 10.1007/s13277-014-1655-0. Epub 2014 Jan 29.

VEGF +405G/C (rs2010963) polymorphisms and digestive system cancer risk: a meta-analysis

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Free article
Meta-Analysis

VEGF +405G/C (rs2010963) polymorphisms and digestive system cancer risk: a meta-analysis

Qing Guo et al. Tumour Biol. 2014 May.
Free article

Abstract

Vascular endothelial growth factor (VEGF) polymorphisms, specifically +405G/C (rs2010963), reportedly influence the risk for various digestive cancers. However, the consequences of these polymorphisms remain controversial and ambiguous. Therefore, we performed a meta-analysis of 11 studies with VEGF +405G/C genotyping on 2,862 patients and 3,028 controls using the random effects model. We obtained a pooled odds ratio (OR) of 1.04 (95% confidence interval (CI) = 0.86-1.26) for the recessive genetic model, 1.07 (95% CI = 0.81-1.42) for the dominant genetic model, 1.09 (95% CI = 0.81-1.47) for the homozygote comparison, and 1.03 (95% CI = 0.83-1.27) for the heterozygote comparison. In the subgroup analysis of the recessive model, the OR was 1.20 (95% CI = 1.02-1.40) in colorectal cancer. These results show that VEGF +405G/C polymorphisms are unlikely to be a major determinant of susceptibility to digestive cancer. Furthermore, the subgroup analysis of recessive model indicates that VEGF +405G/C polymorphisms increase the risk for colorectal cancer.

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