Abstract
Background: Helicobacter pylori, a known risk factor of gastric cancer, rarely colonize the deeper portion of normal gastric glands, where the mucus is rich in α-1,4-linked N-acetylglucosamine capped O-glycans, that strongly inhibit H. pylori growth in vitro. Materials and methods: We investigated the association between genetic variation in the O-glycan transferase encoding gene (a4GnT) and H. pylori infection and gastric cancer risk using a Polish population-based case-control study (273 gastric cancer patients and 377 controls). Results: A haplotype at the rs2622694-rs397266 locus was associated with H. pylori infection, with the A-A haplotype associated with a higher risk compared with the most frequent G-G haplotype (odds ratio 2.30; 95% confidence interval 1.35-3.92). The association remained significant after correction for multiple tests (global p value: nominal 0.002, empirical 0.045). Neither this haplotype nor the tagSNPs were associated with overall gastric cancer risk. Conclusion: a4GnT genetic variation may be relevant to H. pylori infection, but not to gastric cancer risk.
Original language | English (US) |
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Pages (from-to) | 472-477 |
Number of pages | 6 |
Journal | Helicobacter |
Volume | 14 |
Issue number | 5 |
DOIs | |
State | Published - Oct 2009 |
Keywords
- Gastric cancer
- Genetic susceptibility
- Helicobacter pylori
ASJC Scopus subject areas
- Gastroenterology
- Infectious Diseases