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Ornithine decarboxylase inhibitor lessens the rat gastric carcinogenesis enhancement caused by tyrosine methyl ester
Author(s) -
Iishi Hiroyasu,
Tatsuta Masaharu,
Baba Miyako,
Yano Hiroyuki,
Sakai Noriko,
Uehara Hiroyuki,
Nakaizumi Akihiko
Publication year - 1997
Publication title -
international journal of cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.475
H-Index - 234
eISSN - 1097-0215
pISSN - 0020-7136
DOI - 10.1002/(sici)1097-0215(19970926)73:1<113::aid-ijc17>3.0.co;2-h
Subject(s) - ornithine decarboxylase , antrum , endocrinology , stomach , medicine , gastric mucosa , oral administration , histamine , tyrosine , chemistry , biology , biochemistry , enzyme
The effects of combined administration of a catecholamine precursor, tyrosine methyl ester (TME), and an ornithine decarboxylase (ODC) inhibitor, 1,3‐diaminopropane (DAP), on the incidence of gastric cancers induced by N ‐methyl‐ N ′‐nitro‐ N ‐nitrosoguanidine (MNNG), the norepinephrine (NE) concentration and ODC activity of the gastric wall, and the labeling index of the gastric mucosa were investigated in inbred Wistar rats. Rats received s.c. injections of TME, 512 mg/kg body weight, every other day and drinking water with or without 2.5 g/l of DAP after 25 weeks of oral administration of MNNG. At week 52, administration of TME resulted in significant increases in the incidence of gastric cancers, in the NE concentration and the ODC activity of the antral portion of the gastric wall, and in the labeling index of antral epithelial cells. Administration of both TME and DAP significantly reduced the enhancements by TME of gastric carcinogenesis, NE concentration and ODC activity of the antral wall, and the labeling index of the antral mucosa. Our results suggest that ODC inhibition lessens enhancement by TME of gastric carcinogenesis and that the enhancement by TME of gastric carcinogenesis is mediated in part by polyamine biosynthesis. Int. J. Cancer 73:113–116, 1997. © 1997 Wiley‐Liss, Inc.