Pretreatment tumor prostaglandin E2 concentration and cyclooxygenase-2 expression are not associated with the response of canine naturally occurring invasive urinary bladder cancer to cyclooxygenase inhibitor therapy

Prostaglandins Leukot Essent Fatty Acids. 2005 Mar;72(3):181-6. doi: 10.1016/j.plefa.2004.10.017.

Abstract

The purpose of this study was to determine the extent to which pretreatment prostaglandin E2 (PGE2) concentration and cyclooxygenase-2 (cox-2) expression could be used to predict the antitumor activity of cox inhibitor treatment in naturally occurring canine transitional cell carcinoma of the urinary bladder (TCC). Snap frozen tissues (to measure PGE2) and formalin-fixed TCC samples (for cox-2 immunohistochemistry) were obtained by cystoscopy or surgery. Complete tumor staging was performed before and after one month of treatment with the cox inhibitor, piroxicam (0.3 mg/kg q24 h po). The pretreatment PGE2 concentration ranged from 57 to 1624 ng/g of TCC tissue; n=18 dogs). Cox-2 immunoreactivity was observed in all TCC samples. There was no association between PGE2 concentration, cox-2 expression, and change in tumor volume with piroxicam treatment. In conclusion, cox-2 expression or PGE2 concentration alone, or the combination of the two was not useful in predicting response to piroxicam treatment in canine TCC.

MeSH terms

  • Animals
  • Carcinoma, Transitional Cell / drug therapy
  • Carcinoma, Transitional Cell / enzymology
  • Carcinoma, Transitional Cell / metabolism*
  • Cyclooxygenase 2 / biosynthesis*
  • Cyclooxygenase 2 Inhibitors / therapeutic use
  • Dinoprostone / metabolism*
  • Dogs
  • Immunohistochemistry
  • Piroxicam / therapeutic use*
  • Urinary Bladder Neoplasms / drug therapy
  • Urinary Bladder Neoplasms / enzymology*

Substances

  • Cyclooxygenase 2 Inhibitors
  • Piroxicam
  • Cyclooxygenase 2
  • Dinoprostone