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PMID: 10582676 Published · ppublish English Journal Article

Expression of cyclooxygenase-2 (COX-2) in human invasive transitional cell carcinoma (TCC) of the urinary bladder.

Cancer research ·Vol. 59 ·No. 22 ·1999-11-15 ·Pages 5647-50

Mohammed SI, Knapp DW, Bostwick DG, Foster RS, Khan KN, Masferrer JL, Woerner BM, Snyder PW, Koki AT

Abstract

Cyclooxygenase (COX)-inhibiting drugs have antitumor activity in canine and rodent models of urinary bladder cancer. Two isoenzymes of COX have been identified, COX-1 and COX-2. The purpose of this study was to characterize COX-1 and COX-2 expression in human invasive transitional cell carcinoma of the urinary bladder by immunohistochemistry and Western blot analysis. COX-2 was not expressed in normal urinary bladder samples but was detected in 25 of 29 (86%) invasive transitional cell carcinomas of the urinary bladder and in 6 of 8 (75%) cases of carcinoma in situ. These results indicate that COX-2 may play a role in bladder cancer in humans and support further study of COX-2 inhibitors as potential antitumor agents in human bladder cancer.

MeSH Terms
Aged Blotting, Western Carcinoma in Situ/enzymology Carcinoma, Transitional Cell/enzymology Cyclooxygenase 1 Cyclooxygenase 2 Female Humans Immunohistochemistry Isoenzymes/analysis Male Membrane Proteins Middle Aged Neoplasm Proteins/analysis Prostaglandin-Endoperoxide Synthases/analysis Urinary Bladder Neoplasms/enzymology
Chemicals
Isoenzymes Membrane Proteins Neoplasm Proteins Cyclooxygenase 1 Cyclooxygenase 2 PTGS1 protein, human PTGS2 protein, human Prostaglandin-Endoperoxide Synthases
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Mohammed S I
Department of Veterinary Clinical Sciences, Purdue University, West Lafayette, Indiana 47907, USA.
Knapp D W
Bostwick D G
Foster R S
Khan K N
Masferrer J L
Woerner B M
Snyder P W
Koki A T
Article Info
Journal
Cancer research
Abbr.
Cancer Res
ISSN
0008-5472
Published
1999-11-15
Pages
5647-50
Language
English
Region
United States
NLM ID
2984705R
Subset
IM
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