American Journal of Veterinary Research · 2000 · 152 citations · 15 references
MedicineOncologyPharmacologyCarcinogenesisMetastasisNeoplasiaBladder CancerCancer BiomarkersCancer ProgressionEpithelial TumorsMetastatic Urologic CancerUrothelial CarcinomaCanine Transitional Cell CarcinomaCanine Tumor PathologyCyclooxygenase IsoformsMetastatic Bladder CancerMetastatic MechanismsNeoplastic Disease
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.
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Cyclooxygenase in biology and disease
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