A meta-analysis of interleukin-10 -592 promoter polymorphism associated with gastric cancer risk

PLoS One. 2012;7(7):e39868. doi: 10.1371/journal.pone.0039868. Epub 2012 Jul 31.

Abstract

We aimed to explore the role of IL-10 -592 A/C SNP in the susceptibility to gastric cancer through a systematic review and meta-analysis. Each initially included article was scored for quality appraisal. 17 studies were eligible for the meta-analysis. We adopted the most probably appropriate genetic model (recessive model). Potential sources of heterogeneity were sought out via subgroup and sensitivity analyses, and publication biases were estimated. IL-10-592 AA genotype is associated with the reduced risk of developing gastric cancer among Asians and even apparently observed among Asians high quality subgroup, suggesting IL-10-592 AA genotype may seem to be more protective from overall gastric cancer in Asian populations. IL-10-592 AA genotype is also associated with the overall reduced gastric cancer susceptibility in persons with H. pylori infection compared with controls without H. pylori infection, suggesting IL-10-592 AA genotype may seem to be more protective from overall gastric cancer susceptibility in persons infected with H. pylori. IL-10-592 AA genotype is not associated with either pathologic subtypes (intestinal or diffuse) or anatomic subtypes (non-cardia or cardia) of gastric cancer susceptibility. Genotyping methods like direct sequencing should be highly advocated to be conducted in future well-designed high quality studies among different ethnicities or populations.

Publication types

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

MeSH terms

  • Case-Control Studies
  • Genetic Association Studies
  • Genetic Predisposition to Disease
  • Helicobacter Infections / complications
  • Helicobacter Infections / genetics
  • Humans
  • Interleukin-10 / genetics*
  • Odds Ratio
  • Polymorphism, Single Nucleotide*
  • Promoter Regions, Genetic*
  • Publication Bias
  • Risk
  • Stomach Neoplasms / genetics*
  • Stomach Neoplasms / microbiology

Substances

  • IL10 protein, human
  • Interleukin-10

Grants and funding

This work was supported by The National Basic Research Program of China 973 program (2010CB5293), the National High Technology Research and Development Program of China (863 Program) (2006AA02A402), and Science and Technology Commission of Shanghai Municipality (09DZ1950101) to FJY. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.