Association between angiotensin I-converting enzyme gene polymorphism and susceptibility to cancer: a meta analysis

Int J Clin Exp Pathol. 2014 Aug 15;7(9):6291-300. eCollection 2014.

Abstract

Background: Angiotensin I-converting enzyme (ACE) gene plays an important role in the pathogenesis of cancers. The association between ACE insertion/deletion (I/D) polymorphism and the risk of various cancers has been studied. However, the results of these studies remain conflicting. Therefore, we performed a meta-analysis to evaluate the association between ACE I/D polymorphism and the risk of cancers.

Methods: PubMed, Embase, ScienceDirect, Springer, CNKI, Wanfang, Weipu, CBM databases and Google Scholar were searched for case-control studies on ACE I/D polymorphism and the risk of cancers, published up to Dec 31, 2013. Odds ratios (ORs) with 95% confidence intervals (CIs) were used to assess the strength of the association between ACE I/D polymorphism and cancer risk.

Results: Thirty-five published studies with 5007 cases and 8173 controls were included. Overall, there were no significant association between ACE I/D polymorphism and the risk of cancers (II vs. ID+DD OR = 1.05, 95% CI = 0.89-1.23, I vs. D OR = 1.00, 95% CI = 0.89-1.13). However, when stratified by ethnicity, we found a significant association between this polymorphism and cancer risk in Caucasians (II vs. ID+DD: OR = 1.43, 95% CI = 1.02-2.00, I vs. D: OR = 1.23, 95% CI 1.01-1.49).

Conclusion: ACE I/D polymorphism is associated with the cancer risk in Caucasians.

Keywords: ACE I/D; cancer risk; meta-analysis; single nucleotide polymorphism.

Publication types

  • Meta-Analysis
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Case-Control Studies
  • Chi-Square Distribution
  • Gene Frequency
  • Genetic Predisposition to Disease
  • Humans
  • Neoplasms / enzymology
  • Neoplasms / ethnology
  • Neoplasms / genetics*
  • Odds Ratio
  • Peptidyl-Dipeptidase A / genetics*
  • Phenotype
  • Polymorphism, Genetic*
  • Risk Assessment
  • Risk Factors
  • White People / genetics

Substances

  • ACE protein, human
  • Peptidyl-Dipeptidase A