1. [Effects of nonsteroidal anti-inflammatory drug celecoxib on expression of cyclooxygenase-2 (COX-2) in ovarian carcinoma cell].
- Author
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Wang HJ, Liu XJ, Yang KX, Luo FM, Lou JY, and Peng ZL
- Subjects
- Animals, Celecoxib, Cell Line, Tumor, Cyclooxygenase 2 genetics, Cystadenocarcinoma, Serous enzymology, Cystadenocarcinoma, Serous pathology, Female, Humans, Mice, Mice, Inbred BALB C, Mice, Nude, Neoplasm Transplantation, Ovarian Neoplasms pathology, Tumor Cells, Cultured, Anti-Inflammatory Agents, Non-Steroidal pharmacology, Cyclooxygenase 2 biosynthesis, Ovarian Neoplasms enzymology, Pyrazoles pharmacology, Sulfonamides pharmacology
- Abstract
Objective: To explore the effects of nonsteroidal anti-inflammatory drug Celecoxib on the expression of cyclooxygenase-2 (COX-2) in the SKOV3 cell line and the xenografted nude mice of ovarian carcinoma., Methods: The expression of COX-2 in the SKOV3 cell was determined by reverse transcription polymerase chain reaction (RT-PCR), flow cytometry (FCM), and Western blot analysis. The expression of COX-2 in tumor cells was measured with Immunocytochemistry., Results: RT-PCR showed that the expression COX-2 mRNA was strongly down-regulated in SKOV3 cells after treatment with Celecoxib or Aspirin. FCM and Western blot analysis showed that the protein product of COX-2 was strongly decreased by Celecoxib or Aspirin. The Celecoxib was more potential effects than Aspirin. The immunocytochemistry result showed that the expression of COX-2 in 10, 25, 50 mg/kg x d of Celecoxib were lower obviously than it in the control group in Xenografted nude mice., Conclusion: The anticarcinogenic effects of Celecoxib is probably related to the down-regulation of COX-2, and can be explained to both COX-2-dependent and -independent mechanisms.
- Published
- 2006