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Georgia Veterinary Scholar |
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Kendall Flynt |
Dr. Bruce LeRoy UGA College of Veterinary Medicine |
In Vitro Effects of a Selective COX-2 Inhibitor on Canine Prostate Cancer Cell Growth
* J. Flynt, B. LeRoy
Cyclooxygenase-2 (COX-2) inhibitors are useful adjunct therapies for treating a wide variety of neoplasms in humans and animals. Previous studies have shown that COX-2 inhibitors can reduce tumor size through decreasing cell proliferation. We used an in vitro assay to determine the effects of a selective cyclooxygenase inhibitor, deracoxib, on the proliferation and growth of a canine prostate cancer cell line. An agarose gel assay was prepared with Dulbecco’s modified Eagle medium(DMEM) in 12-well microplates. Canine prostate carcinoma cells were suspended in agarose at 5 different concentrations ranging from 1x103cells/mL to 2.0x104cells/mL. After 24 hours of incubation, the cells were treated with concentrations of derocoxib ranging from 0.5mM to 500.0mM. Control cells received vehicle only. On post-treatment days 1, 3, 6, and 9, cells were examined under light microscopy and colonies of cells ≥0.0125mm in size were counted. We found that deracoxib-treated cells showed an increase in proliferation with the exception of the highest concentration of deracoxib, 500.0mM, which has been previously shown to be a toxic level to cells. Our data shows that COX-2 inhibitors appear to stimulate canine prostate cancer cell proliferation at therapeutic levels and could be useful adjunct therapies to increase the effectiveness of traditional cytotoxic chemotherapy drugs.


