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Roles of cyclooxygenase-2 and microsomal prostaglandin E synthase-1 expression and beta-catenin activation in gastric carcinogenesis in N-methyl-N-nitrosourea-treated K19-C2mE transgenic mice.

Abstract
K19-C2mE transgenic (Tg) mice, simultaneously expressing cyclooxygenase-2 (COX-2) and microsomal prostaglandin E synthase-1 (mPGES-1) in the gastric mucosa under the cytokeratin 19 gene promoter, were here treated with N-methyl-N-nitrosourea (MNU) and inoculated with Helicobacter pylori (H. pylori) to investigate gastric carcinogenesis. Wild-type (WT) and Tg mice undergoing MNU treatment frequently developed tumors in the pyloric region (100% and 94.7%, respectively); multiplicity in Tg was higher than that in WT (P < 0.05) with H. pylori infection. Larger pyloric tumors were more frequently observed in Tg than in WT (P < 0.05). In addition, Tg developed fundic tumors, where WT did not. No gastric tumors were observed without MNU treatment. Transcripts of TNF-alpha, iNOS, IL-1beta, and CXCL14 were up-regulated with H. pylori infection in both genotypes and were also increased more in Tg than in WT within H. pylori-inoculated animals. Immunohistochemical analysis demonstrated significantly greater beta-catenin accumulation in pyloric tumors, compared with those in the fundus (P < 0.01) with mutations of exon 3; 18.2% and 31.6% in MNU-alone and MNU + H. pylori-treated WT, whereas 21.4% and 62.5% was observed in the Tg, respectively; the latter significantly higher (P < 0.05), suggesting the role of H. pylori in Wnt activation. In conclusion, K19-C2mE mice promoted gastric cancer in both fundic and pyloric regions. Furthermore beta-catenin activation may play the important role of pyloric carcinogenesis especially in H. pylori-infected Tg. Induction of various inflammatory cytokines in addition to overexpression of COX-2/mPGES-1 could be risk factors of gastric carcinogenesis and may serve as a better gastric carcinogenesis model.
AuthorsShinji Takasu, Tetsuya Tsukamoto, Xue-Yuan Cao, Takeshi Toyoda, Akihiro Hirata, Hisayo Ban, Masami Yamamoto, Hiroki Sakai, Tokuma Yanai, Toshiaki Masegi, Masanobu Oshima, Masae Tatematsu
JournalCancer science (Cancer Sci) Vol. 99 Issue 12 Pg. 2356-64 (Dec 2008) ISSN: 1349-7006 [Electronic] England
PMID19018769 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Carcinogens
  • beta Catenin
  • Methylnitrosourea
  • Cyclooxygenase 2
  • Intramolecular Oxidoreductases
  • Prostaglandin-E Synthases
  • Ptges protein, mouse
Topics
  • Animals
  • Carcinogens (pharmacology)
  • Cell Transformation, Neoplastic (drug effects)
  • Cyclooxygenase 2 (genetics, metabolism)
  • Enzyme Activation
  • Gastric Mucosa (metabolism, pathology)
  • Helicobacter Infections (complications)
  • Helicobacter pylori (pathogenicity)
  • Immunohistochemistry
  • Intramolecular Oxidoreductases (genetics, metabolism)
  • Methylnitrosourea (pharmacology)
  • Mice
  • Mice, Transgenic
  • Microsomes
  • Prostaglandin-E Synthases
  • Random Allocation
  • Stomach Neoplasms (etiology, genetics, metabolism, pathology)
  • beta Catenin (metabolism)

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