Helicobacter pylori infection and expression of DNA mismatch repair proteins

World J Gastroenterol. 2008 Nov 21;14(43):6717-21. doi: 10.3748/wjg.14.6717.

Abstract

Aim: To determine the expression of DNA (MMR) proteins, including hMLH1 and hMSH2, in gastric epithelial cells in the patients with or without Helicobacter pylori (H pylori)-infected gastritis.

Methods: Fifty H pylori-positive patients and 50 H pylori-negative patients were enrolled in the study. During endoscopy of patients with non-ulcer dyspepsia, two antral and two corpus biopsies were taken for histological examination (Giemsa stain) and for immunohistochemical staining of hMLH1 and hMSH2.

Results: The percentage of epithelial cell nuclei that demonstrated positivity for hMLH1 staining was 84.14 +/- 7.32% in H pylori-negative patients, while it was 73.34 +/- 10.10% in H pylori-positive patients (P < 0.0001). No significant difference was seen between the two groups regarding the percentage of epithelial cell nuclei that demonstrated positivity for hMSH2 staining (81.16 +/- 8.32% in H pylori-negative versus 78.24 +/- 8.71% in H pylori-positive patients; P = 0.09).

Conclusion: This study indicates that H pylori might promote development of gastric carcinoma at least in part through its ability to affect the DNA MMR system.

Publication types

  • Comparative Study

MeSH terms

  • Adaptor Proteins, Signal Transducing / metabolism*
  • Adult
  • Biopsy
  • DNA Mismatch Repair / physiology*
  • Epithelium / metabolism
  • Epithelium / pathology
  • Female
  • Gastric Mucosa / metabolism
  • Gastritis / metabolism*
  • Gastritis / pathology
  • Helicobacter Infections / metabolism*
  • Helicobacter Infections / pathology
  • Helicobacter pylori*
  • Humans
  • Male
  • Microsatellite Instability
  • Middle Aged
  • MutL Protein Homolog 1
  • MutL Proteins
  • Neoplasm Proteins / metabolism*
  • Nuclear Proteins / metabolism*
  • Stomach / pathology

Substances

  • Adaptor Proteins, Signal Transducing
  • MLH1 protein, human
  • Neoplasm Proteins
  • Nuclear Proteins
  • PMS1 protein, human
  • MutL Protein Homolog 1
  • MutL Proteins