Celecoxib antagonizes the cytotoxic effect of cisplatin in human gastric cancer cells by decreasing intracellular cisplatin accumulation |
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Authors: | Minghui Chen Le Yu Chunping Gu Desheng ZhongShuguang Wu Shuwen Liu |
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Affiliation: | School of Pharmaceutical Sciences, Southern Medical University, Guangzhou 510515, China |
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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. |
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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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