ERCC2 Lys751Gln and Asp312Asn polymorphisms and gastric cancer risk: a meta-analysis

J Cancer Res Clin Oncol. 2011 Jun;137(6):939-46. doi: 10.1007/s00432-010-0956-y. Epub 2010 Oct 28.

Abstract

Purpose: Studies investigating the association between excision repair cross-complimentary group 2 (ERCC2) polymorphisms and gastric cancer (GC) risk have reported conflicting results. We performed a meta-analysis of published epidemiological studies to derive a more precise estimation of the relationship.

Methods: Published literature from PubMed, EMBASE, and China National Knowledge Infrastructure was retrieved. Ten studies with 2,141 GC cases and 5,343 controls were selected.

Results: No association between ERCC2 Lys751Gln polymorphism and GC susceptibility for all genetic models was found. When stratified by race, we found the Gln/Gln genotype carriers might be at high risk of GC among Asians, but not among Caucasians. Also, the pooled results showed there was a significant difference in genotype distribution between non-gastric cardia cancer cases and controls. For ERCC2 Asp312Asn polymorphism, significantly elevated GC risk was associated with Asn/Asn genotype (AA vs. GG + GA: OR = 1.36, 95%CI = 1.04-1.77, P = 0.02). We also found this genotype was associated with GC susceptibility among Asians and subjects without Helicobacter pylori infection. No publication bias was found in the present study.

Conclusions: This meta-analysis concluded that both ERCC2 Lys751Gln and Asp312Asn polymorphisms might contribute to increased risk of GC among Asians.

Publication types

  • Meta-Analysis

MeSH terms

  • Asian People / genetics
  • Genotype
  • Humans
  • Polymorphism, Genetic*
  • Risk
  • Stomach Neoplasms / etiology
  • Stomach Neoplasms / genetics*
  • Xeroderma Pigmentosum Group D Protein / genetics*

Substances

  • Xeroderma Pigmentosum Group D Protein
  • ERCC2 protein, human