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Lack of association between Hsa-Mir-499 rs3746444 polymorphism and cancer risk: meta-analysis findings.

Abstract
Epidemiologic findings concerning the association between the hsa-mir-499 rs3746444 A>G polymorphism and cancer risk have yielded mixed results. We aimed to investigate the association by performing a meta-analysis of all available studies. We searched PubMed and EMBASE for studies published up to November 2014, using odds ratios (ORs) with 95% confidence intervals (CIs) to assess the strength of any association. The Benjamini- Hochberg (BH) method was used to correct the p values for multiple comparisons. We included 39 studies, including 14,136 cases and 16,937 controls. The results of overall meta-analysis suggested a borderline association between hsa-mir-499 rs3746444 polymorphism and cancer susceptibility (AG+GG vs. AA: OR=1.15, 95% CI= 1.04-1.26, corrected p value=0.04). After removing studies not conforming to Hardy-Weinberg equilibrium (HWE), however, this association disappeared (AG+GG vs AA: OR=1.18, 95% CI=1.03-1.34, corrected p value=0.21). When stratified analysis by ethnicity, cancer type or HWE in controls, although some associations between hsa-mir-499 rs3746444 polymorphism and cancer susceptibility were detected, these associations no longer existed after adjustment using BH method. In conclusion, our meta-analysis suggests that hsa-mir-499 rs3746444 A>G polymorphism is not associated with risk of cancer based on current evidence.
AuthorsSheng-Gao Jiang, Lin Chen, Jin-Hai Tang, Jian-Hua Zhao, Shan-Liang Zhong
JournalAsian Pacific journal of cancer prevention : APJCP (Asian Pac J Cancer Prev) Vol. 16 Issue 1 Pg. 339-44 ( 2015) ISSN: 2476-762X [Electronic] Thailand
PMID25640376 (Publication Type: Journal Article, Meta-Analysis)
Chemical References
  • MIRN499 microRNA, human
  • MicroRNAs
Topics
  • Asian People (genetics)
  • Genetic Association Studies
  • Genetic Predisposition to Disease
  • Humans
  • MicroRNAs (genetics)
  • Neoplasms (epidemiology, genetics)
  • Odds Ratio
  • Polymorphism, Single Nucleotide
  • Risk

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