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YI Fang, XU Xin-hua, FU Xiang-yang, DAI De-lan-, LI Dao-jun, ZHANG Chang-ju. Growth Inhibition of Nasopharyngeal Carcinoma Cell Line CNE-2 by Celecoxib[J]. Cancer Research on Prevention and Treatment, 2009, 36(02): 100-102. DOI: 10.3971/j.issn.1000-8578.2009.02.005
Citation: YI Fang, XU Xin-hua, FU Xiang-yang, DAI De-lan-, LI Dao-jun, ZHANG Chang-ju. Growth Inhibition of Nasopharyngeal Carcinoma Cell Line CNE-2 by Celecoxib[J]. Cancer Research on Prevention and Treatment, 2009, 36(02): 100-102. DOI: 10.3971/j.issn.1000-8578.2009.02.005

Growth Inhibition of Nasopharyngeal Carcinoma Cell Line CNE-2 by Celecoxib

  • Objective To investigate the growth of nasopharyngeal carcinoma cell line CNE-2 treated with a selective cyclooxygenase-2 inhibitor, Celecoxib. Methods The cell survival rate was measured by MTT assay, the cell cycle and apoptosis were analyzed using flow cytometric method (FCM), the expression of COX-2 protein in CNE cells treated with Celecoxib was detected by SP method. Results Celecoxib remarkably inhibited the growth and proliferation of CNE-2 tumor cells, which was demonstrated in a time-and dose-dependent effect. The DNA content in each phase of cell cycle has significantly changed as follows; cell numbers in G0~G1 fraction increased significantly (from 47.03% up to the highest percentage of 79.20%), whereas it decreased in S and G2-M phase of cell cycle. Apparently apoptosis was induced in CNE-2 cells by celecoxib. From the result of immunochemistry SP method it suggested that Celecoxib dramatically suppressed the expression of COX-2 in CNE-2 cells. Conclusion Celecoxib effectively inhibited the growth and proliferation of CNE-2 tumor cells which induces accumulation of tumor cells in G0/G1 phase. Importantly, the mechanism of antitumor effect by Celecoxib may include COX-2 dependent ways.
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