[No authors listed]
Previous studies have found inconsistent results regarding gene deletion in APOBEC3 (apolipoprotein B mRNA-editing catalytic polypeptide-like 3) and risk of cancer. We conducted a meta-analysis of all eligible case-control studies to find out the associations between APOBEC3 deletion and cancer risk by pooling the odds ratios (ORs) and corresponding 95% confidence intervals (CIs). Overall, the findings from 20 studies (13 articles) involving of a total of 26Â 225 cases and 37Â 201 controls revealed that DD genotype was associated significantly with increased cancer risk compared to II genotype (ORÂ =Â 1.25, 95% CIÂ =Â 1.01-1.56, PÂ =Â 0.04). Stratified analysis from 10 studies including 14Â 757 cases and 17Â 930 controls revealed that I/D variant significantly increased the risk of breast cancer in heterozygous codominant (ORÂ =Â 1.15, 95% CIÂ =Â 1.03-1.28, PÂ =Â 0.02, ID vs II), dominant (ORÂ =Â 1.15, 95% CIÂ =Â 1.01-1.31, PÂ =Â 0.03, IDÂ +Â DD vs II), overdominant (ORÂ =Â 1.11, 95% CIÂ =Â 1.05-1.25, PÂ <Â 0.0001, ID vs DDÂ +Â II) and allele (ORÂ =Â 1.15, 95% CIÂ =Â 1.13-1.25, PÂ =Â 0.03, D vs I) inheritance models. In conclusion, the data propose that APOBEC3 deletion is significantly associated with increased susceptibility to cancer in overall and breast cancer. Our findings require well-designed replication in a larger independent genetic association study with larger sample sizes in diverse ethnicities.
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