Expression of cyclooxygenase-2 in transitional cell carcinoma of the urinary bladder in dogs

Am J Vet Res. 2000 May;61(5):478-81. doi: 10.2460/ajvr.2000.61.478.

Abstract

Objective: To evaluate expression of cyclooxygenase (COX)-1 and COX-2 in the urinary bladder epithelium of clinically normal dogs and in transitional cell carcinoma cells of dogs.

Animals: 21 dogs with transitional cell carcinoma of the urinary bladder and 8 dogs with clinically normal urinary bladders.

Procedure: COX-1 and COX-2 were evaluated by use of isoform-specific antibodies with standard immunohistochemical methods.

Result: COX-1, but not COX-2, was constitutively expressed in normal urinary bladder epithelium; however, COX-2 was expressed in neoplastic epithelium in primary tumors and in metastatic lesions of all 21 dogs and in new proliferating blood vessels in 3 dogs. Also, COX-1 was expressed in the neoplastic cells.

Conclusions and clinical relevance: Lack of expression of COX-2 in normal bladder epithelium and its substantial expression in transitional cell carcinoma cells suggest that this isoform may be involved in tumor cell growth. Inhibition of COX-2 is a likely mechanism of the antineoplastic effects of non steroidal antiinflammatory drugs.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology
  • Biopsy / veterinary
  • Carcinoma, Transitional Cell / enzymology
  • Carcinoma, Transitional Cell / pathology
  • Carcinoma, Transitional Cell / secondary
  • Carcinoma, Transitional Cell / veterinary*
  • Cyclooxygenase 1
  • Cyclooxygenase 2
  • Cyclooxygenase 2 Inhibitors
  • Cyclooxygenase Inhibitors / pharmacology
  • Disease Models, Animal
  • Dog Diseases / enzymology*
  • Dog Diseases / genetics
  • Dog Diseases / pathology
  • Dogs
  • Epithelium / enzymology
  • Epithelium / pathology
  • Gene Expression Regulation, Enzymologic
  • Gene Expression Regulation, Neoplastic*
  • Immunohistochemistry
  • Isoenzymes / antagonists & inhibitors
  • Isoenzymes / biosynthesis*
  • Isoenzymes / genetics
  • Isoenzymes / pharmacology
  • Lung Neoplasms / enzymology
  • Lung Neoplasms / pathology
  • Lung Neoplasms / secondary
  • Prostaglandin-Endoperoxide Synthases / biosynthesis*
  • Prostaglandin-Endoperoxide Synthases / genetics
  • Prostaglandin-Endoperoxide Synthases / pharmacology
  • Urinary Bladder / enzymology
  • Urinary Bladder / pathology
  • Urinary Bladder Neoplasms / enzymology
  • Urinary Bladder Neoplasms / pathology
  • Urinary Bladder Neoplasms / veterinary*

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Cyclooxygenase 2 Inhibitors
  • Cyclooxygenase Inhibitors
  • Isoenzymes
  • Cyclooxygenase 1
  • Cyclooxygenase 2
  • Prostaglandin-Endoperoxide Synthases