Cytokine polymorphisms and gastric cancer risk: an evolving view

Cancer Biol Ther. 2008 Feb;7(2):157-62. doi: 10.4161/cbt.7.2.5270. Epub 2007 Nov 5.

Abstract

More than 20 years after the identification of Helicobacter pylori as a human pathogen, gastric cancer continues to be a leading cause of cancer deaths worldwide. Genetic association studies have the potential for helping to identify those at greatest risk for developing gastric cancer subsequent to infection by H. pylori. IL1B promoter polymorphisms have been supported by several meta-analyses as being associated with gastric cancer risk. In this review, we discuss challenges in experimental design of gene association studies in gastric cancer, with attention to gene-environment interactions that may lead to inconsistency in findings across populations.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Alleles
  • Cytokines / genetics*
  • Gene Frequency
  • Genetic Heterogeneity
  • Genetic Predisposition to Disease*
  • Helicobacter Infections / genetics*
  • Helicobacter Infections / microbiology
  • Helicobacter pylori / pathogenicity
  • Humans
  • Linkage Disequilibrium
  • Polymorphism, Genetic*
  • Promoter Regions, Genetic
  • Risk Factors
  • Stomach Neoplasms / genetics*
  • Stomach Neoplasms / microbiology

Substances

  • Cytokines