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Celecoxib antagonizes the cytotoxic effect of cisplatin in human gastric cancer cells by decreasing intracellular cisplatin accumulation
Authors:Minghui Chen  Le Yu  Chunping Gu  Desheng ZhongShuguang Wu  Shuwen Liu
Affiliation:School of Pharmaceutical Sciences, Southern Medical University, Guangzhou 510515, China
Abstract:Cisplatin is a chemotherapeutic drug widely used for the treatment of gastric cancer. The benefit of including COX-2-selective inhibitors in cisplatin-based regimens on anti-cancer effect remains uncertain. In the present study, celecoxib and SC-236 antagonized cisplatin-induced cytotoxicity and apoptosis, whereas indomethancin and nimesulide exerted no effect, implying a COX-2-independent mechanism. Celecoxib decreased whole-cell cisplatin accumulation and DNA platination, resulting from reduced influx. In addition, combined treatment did not elicit greater antitumor activity than cisplatin or celecoxib monotherapy in vivo in a gastric xenograft model. Therefore, treatment strategies with celecoxib in combination with cisplatin should act cautiously.
Keywords:COX, cyclooxygenase   CTR1, copper transporter 1   NSAIDs, nonsteroidal anti-inflammatory drugs   PGE2, Prostaglandin E2   PARP, poly (ADP-ribose) polymerase   siRNA, small interference RNA   SC-236, 4-[5-(4-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]benzenesulfonamide
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