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Mucosal expression of cyclooxygenase isoforms 1 and 2 is increased with worsening damage to the gastric mucosa
Author(s) -
Bhandari P,
Bateman A C,
Mehta R L,
Patel P
Publication year - 2005
Publication title -
histopathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.626
H-Index - 124
eISSN - 1365-2559
pISSN - 0309-0167
DOI - 10.1111/j.1365-2559.2005.02053.x
Subject(s) - lamina propria , gastritis , gastric mucosa , immunohistochemistry , medicine , atrophic gastritis , pathology , cyclooxygenase , stomach , gastroenterology , biology , epithelium , enzyme , biochemistry
Aims : To test the hypothesis that both COX‐1 and COX‐2 expression in human gastric mucosa is up‐regulated in the presence of inflammation as seen in patients with gastritis and gastric ulcers. Methods and results : We performed immunohistochemistry using COX‐1 and COX‐2 monoclonal antibodies on gastric biopsies from 59 patients with normal mucosa, gastritis and gastric ulcers. Expression of COX‐1 and COX‐2 was quantified using an intensity proportion scoring system. Expression of COX‐1 was primarily seen in the lamina propria mononuclear cells with some expression in deep gastric glands in the ulcer group. Expression of COX‐2 was primarily seen in the deep gastric glands with focal expression in the lamina propria mononuclear cells. We found a stepwise increase in the expression of both COX‐1 and COX‐2 as mucosal damage progressed from normal to gastritis to gastric ulcer. Conclusions : We conclude that both COX‐1 and COX‐2 expression in the gastric mucosa are increased in the setting of gastritis and gastric ulceration. Although this increased expression may be due, at least in part, to an increase in inflammatory cell numbers, this study raises the possibility that both COX‐1 and COX‐2 are inducible, contrary to the traditionally held view of only COX‐2 being inducible.