[Expression of cyclooxygenase in bladder transitional cell carcinoma]

Sichuan Da Xue Xue Bao Yi Xue Ban. 2004 Jan;35(1):54-6.
[Article in Chinese]

Abstract

Objective: To evaluate the role of cyclooxygenase-1 (COX-1) and cyclooxygenase-2 (COX-2) in the development of bladder transitional cell carcinoma.

Methods: Thirty-four specimens were obtained from patients with bladder transitional carcinoma, and 7 specimens of normal bladder tissues were obtained from renal transplantation donors. Immunohistochemistry and RT-PCR were performed to study the expression of COX-1 and COX-2.

Results: No marked expression of COX-2 was observed in the normal bladder, but higher level of COX-2 expression was noted in the malignant cells. The extent and intensity of COX-2 expression in cancer cells were statistically greater than those in the cells from normal bladder tissue. Correlation between COX-2 expression and progression of bladder transitional cell carcinoma was observed. COX-2 expression was significantly higher in Grade 3 bladder transitional cell carcinoma than in Grades 1 and 2 (P < 0.001). There was no significant difference in COX-2 expression level between the bladder transitional cell carcinomas at different clinical stages (P > 0.05). The expression of COX-1 was seen in some bladder transitional cell carcinoma and normal bladder.

Conclusion: COX-2 might be of significance to the proliferation and development of bladder transitional cell carcinoma.

Publication types

  • English Abstract

MeSH terms

  • Adult
  • Aged
  • Carcinoma, Transitional Cell / metabolism*
  • Cell Division
  • Cyclooxygenase 1
  • Cyclooxygenase 2
  • Female
  • Humans
  • Isoenzymes / biosynthesis*
  • Isoenzymes / genetics
  • Male
  • Membrane Proteins
  • Middle Aged
  • Neoplasm Staging
  • Prostaglandin-Endoperoxide Synthases / biosynthesis*
  • Prostaglandin-Endoperoxide Synthases / genetics
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / genetics
  • Tumor Cells, Cultured
  • Urinary Bladder Neoplasms / metabolism*

Substances

  • Isoenzymes
  • Membrane Proteins
  • RNA, Messenger
  • Cyclooxygenase 1
  • Cyclooxygenase 2
  • PTGS1 protein, human
  • PTGS2 protein, human
  • Prostaglandin-Endoperoxide Synthases