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Am J Physiol Gastrointest Liver Physiol 290: G519-G527, 2006. First published October 27, 2005; doi:10.1152/ajpgi.00113.2005
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MUCOSAL BIOLOGY

Involvement of cyclooxygenase-2 in gastric mucosal hypertrophy in gastrin transgenic mice

Naoki Kanda,1 Hiroshi Seno,1 Mayumi Kawada,1 Tateo Sawabu,1 Yoshito Uenoyoma,1 Toshio Nakajima,1 Yoshitaka Konda,1 Hirokazu Fukui,1 Toshiyuki Takeuchi,2 and Tsutomu Chiba1

1Department of Gastroenterology and Hepatology, Kyoto University Graduate School of Medicine, Kyoto; and 2Department of Molecular Medicine, Institute of Molecular and Cellular Regulation, Gunma University, Maebashi, Japan

Submitted 15 March 2005 ; accepted in final form 26 October 2005

Gastrin promotes gastric mucosal growth, and hypergastrinemia induces gastric mucosal hypertrophy. Recently, it has been reported that gastrin induces cyclooxygenase-2 (COX-2) in human gastric and colorectal cancer cell lines. However, whether COX-2 is involved in gastrin-induced gastric mucosal growth in vivo is unknown. We investigated the role of COX-2 in gastrin-induced gastric mucosal hypertrophy using gastrin transgenic mice. Hypergastrinemic mice [mice with mutated gastrin under the control of the beta-actin promoter (ACT-GAS mice)] received the COX-2 inhibitor celecoxib (0, 200, or 500 mg/kg of diet) from 5 wk of age and were killed at 16 or 24 wk. Some ACT-GAS mice received celecoxib from 16 wk and were killed at 24 wk. Eighty-week-old ACT-GAS mice without celecoxib treatment were also examined. The thickness of the gastric mucosa, cell populations, COX-2 expression, and PGE2 levels were evaluated. All ACT-GAS mice showed gastric mucosal hypertrophy, and four of six 80-wk-old ACT-GAS mice developed gastric cancer. COX-2 was expressed in interstitial cells of the hypertrophic gastric mucosa and gastric cancers. Moreover, PGE2 levels in the gastric mucosa of ACT-GAS mice were significantly higher than those of normal mice. With treatment with celecoxib, PGE2 levels, the gastric mucosal thickness, and the number of total gastric cells per gastric gland of ACT-GAS mice were significantly decreased. The decrease in gastric mucosal thickness was caused by a reduction of foveolar hyperplasia. The thickness of glandules and the number of Ki67-positive cells were not significantly changed. In conclusion, COX-2 contributes to gastrin-induced mucosal hypertrophy of the stomach.

prostaglandin E2; gastric cancer; foveolar hyperplasia



Address for reprint requests and other correspondence: H. Seno, Dept. of Gastroenterology and Hepatology, Kyoto Univ. Graduate School of Medicine, Shogoin-Kawara-cho 54, Sakyo-ku, Kyoto 606-8507, Japan (e-mail: seno{at}kuhp.kyoto-u.ac.jp)




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Am. J. Physiol. Gastrointest. Liver Physiol.Home page
S. Tu, A. L. Chi, S. Lim, G. Cui, Z. Dubeykovskaya, W. Ai, J. V. Fleming, S. Takaishi, and T. C. Wang
Gastrin regulates the TFF2 promoter through gastrin-responsive cis-acting elements and multiple signaling pathways
Am J Physiol Gastrointest Liver Physiol, June 1, 2007; 292(6): G1726 - G1737.
[Abstract] [Full Text] [PDF]




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