Relationship of Helicobacter pylori CagA status to gastric cell proliferation and apoptosis

Citation
T. Rokkas et al., Relationship of Helicobacter pylori CagA status to gastric cell proliferation and apoptosis, DIG DIS SCI, 44(3), 1999, pp. 487-493
Citations number
55
Categorie Soggetti
Gastroenerology and Hepatology","da verificare
Journal title
DIGESTIVE DISEASES AND SCIENCES
ISSN journal
01632116 → ACNP
Volume
44
Issue
3
Year of publication
1999
Pages
487 - 493
Database
ISI
SICI code
0163-2116(199903)44:3<487:ROHPCS>2.0.ZU;2-O
Abstract
Despite the fact that the association of Helicobacter pylori with an increa sed risk of gastric cancer is well documented, the exact mechanisms of this association have not been elucidated. Our aim was to shed some light on th ese mechanisms by studying the relationship of H. pylori CagA status to gas tric cell proliferation and apoptosis, since both play an important role in gastrointestinal epithelial cell turnover and carcinogenesis. We studied f ifty patients [32 men, 18 women, median age 39.5 years (range 18-67)], refe rred for upper gastrointestinal endoscopy, from whom antral biopsies were t aken. On biopsy specimens gastritis was estimated by scoring the severity o f inflammatory infiltrate, and the presence of atrophy and intestinal metap lasia were also noted. The gastric cell proliferation index (PI) was estima ted by AgNOR staining, the epithelial apoptotic index (AI) was measured by special staining for apoptosis, and CagA status was determined serologicall y by immunoblotting the sera of patients against H, pylori antigens. Thirty -eight (76%) of the 50 patients were H; pylori (positive) and 12 (24%) H. p ylori (negative). Among the 38 H. pylori(+) patients, 28 (73.6%) were CagA( +) and 10 (24.6%) CagA(-). In the H. pylori CagA(+) and CagA(-) groups, the PI values [median (ranges)] were 5 (4-7) and 3.7 (3.5-5.5), respectively ( P < 0.05). In addition the difference in PI between the H. pylori CagA(+) a nd H. pylori(-) groups was highly significant (P < 0.001). Concerning apopt osis, in the H. pylori CagA(+) and CagA(-) groups, the values for AI were 1 (1-30) and 5.5 (1-35), respectively (P < 0.05). In addition, the differenc e in AI between the H. pylori CagA(-) and H. pylori(-) groups, was signific ant (P < 0.05). We conclude that H. pylori CagA(+) strains induce increased gastric cell proliferation, which is not accompanied by a parallel increas e in apoptosis. This might explain the increased risk for gastric carcinoma that is associated with infection by H. pylori CagA(+) strains.