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Stepwise cumulation of RUNX3 methylation mediated by Helicobacter pylori infection contributes to gastric carcinoma progression
Article first published online: 10 MAY 2012
Copyright © 2012 American Cancer Society
Volume 118, Issue 22, pages 5507–5517, 15 November 2012
How to Cite
Lu, X.-X., Yu, J.-L., Ying, L.-S., Han, J., Wang, S., Yu, Q.-M., Wang, X.-B., Fang, X.-H. and Ling, Z.-Q. (2012), Stepwise cumulation of RUNX3 methylation mediated by Helicobacter pylori infection contributes to gastric carcinoma progression. Cancer, 118: 5507–5517. doi: 10.1002/cncr.27604
- Issue published online: 30 OCT 2012
- Article first published online: 10 MAY 2012
- Manuscript Accepted: 22 MAR 2012
- Manuscript Revised: 16 MAR 2012
- Manuscript Received: 25 JAN 2012
- gastric carcinoma;
- runt-related transcription factor 3;
- promoter methylation;
- Helicobacter pylori infection;
- tumor progression
Helicobacter pylori has been recognized as a definite carcinogen for gastric cancer (GC); however, the pathogenesis of H. pylori infection remains unclear. Runt-related transcription factor 3 (RUNX3) is a candidate tumor suppressor gene whose deficiency is causally related to GC. However, in H. pylori infection-associated GC, the role of RUNX3 has not been studied.
The authors used real-time methylation-specific polymerase chain reaction analysis to determine methylation status of the RUNX3 promoter in a spectrum of gastric lesions, including 220 samples of chronic atrophic gastritis, 196 samples of intestinal metaplasia, 134 samples of gastric adenoma, 102 samples of dysplasia, and 202 samples of GC with paired noncancerous mucosa tissues and corresponding blood specimens. The association of abnormal methylation with precancerous gastric lesions was evaluated along with the association between RUNX3 methylation and H. pylori infection, and the concordance of methylation levels was investigated between serum and tissues.
The results indicated that increasing RUNX3 promoter methylation was correlated with distinct stages of GC progression. GC tissues had the highest methylation proportion (75.2%) compared with precancerous gastric lesions, including chronic atrophic gastritis (15.9%), intestinal metaplasia (36.7%), gastric adenoma (41.8%), and dysplasia (54.9%). H. pylori infection, a major risk factor for GC, contributed to the inactivation of RUNX3 in gastric epithelial cells through promoter hypermethylation. The levels of RUNX3 methylation in serum were in significant concordance with the methylation levels observed in GC tissues (P = .887).
The current findings supported RUNX3 methylation as a risk factors for the carcinogenesis of chronic atrophic gastritis with H. pylori infection and indicated that circulating RUNX3 methylation is a valuable biomarker for the detection of early GC. Cancer 2012. © 2012 American Cancer Society.