UMMS Affiliation

Division of Gastroenterology; Division of Digestive Diseases and Nutrition

Date

11-19-2004

Document Type

Article

Subjects

Animals; Disease Susceptibility; Gastrins; Glycine; Mice; Mice, Transgenic; Parietal Cells, Gastric; Peptic Ulcer; Stomach

Disciplines

Cancer Biology | Digestive System Diseases | Molecular, Genetic, and Biochemical Nutrition

Abstract

Recently we have reported synergistic effects between glycine-extended gastrin (G-gly) and amidated gastrin-17 on acid secretion in short-term infusion studies. In the present study, we examined the long-term effect of G-gly on the atrophy-promoting effects of amidated gastrin in the mouse stomach with or without Helicobacter infection. Transgenic mice overexpressing amidated gastrin (INS-GAS mice), G-gly (MTI/G-gly mice), and both peptides (INS-GAS/G-gly mice) were used for assessment of acid secretion and ulcer susceptibility and histologic examination and scoring of preneoplastic lesions in response to the 3 and 6 months Helicobacter felis (H. felis) infection. We found that MTI/G-gly mice had normal gastric histology and acid secretion. Double transgenic (INS-GAS/G-gly) mice showed 2-fold increases in acid secretion compared with INS-GAS mice. Acute peptic ulcers after pyloric ligation were noted in 50% of the INS-GAS/G-gly mice but in none of the INS-GAS mice at 6 months of age. Whereas male INS-GAS mice had a >50% decrease in the numbers of parietal cell and enterochromaffin-like cell at 6 months of age, the male double transgenic mice had no such decrease. Overexpression of G-gly reduced the scores of preneoplasia in the stomach; however, it did not prevent the development of amidated gastrin-dependent gastric cancer in both H. felis-infected mice and uninfected mice. We conclude that G-gly synergizes with amidated gastrin to stimulate acid secretion and inhibits parietal cell loss in INS-GAS/G-gly mice. The overexpression of G-gly seems to increase the susceptibility to peptic ulcer disease and delay the development of Helicobacter-mediated gastric preneoplasia in this model.

Rights and Permissions

Citation: Cancer Res. 2004 Nov 15;64(22):8160-6. Link to article on publisher's site

DOI of Published Version

10.1158/0008-5472.CAN-04-0876

Related Resources

Link to article in PubMed

Journal Title

Cancer research

PubMed ID

15548680

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