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塞来昔布对鼻咽癌CNE-2细胞增殖抑制的实验研究[J]. 肿瘤防治研究, 2009, 36(02): 100-102. DOI: 10.3971/j.issn.1000-8578.2009.02.005
引用本文: 塞来昔布对鼻咽癌CNE-2细胞增殖抑制的实验研究[J]. 肿瘤防治研究, 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[J]. Cancer Research on Prevention and Treatment, 2009, 36(02): 100-102. DOI: 10.3971/j.issn.1000-8578.2009.02.005
Citation: 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

塞来昔布对鼻咽癌CNE-2细胞增殖抑制的实验研究

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

  • 摘要: 目的 研究环氧化酶-2抑制剂塞来昔布对鼻咽癌细胞CNE-2增殖的影响。方法 采用MTT法测定细胞代谢率,以流式细胞术观察细胞DNA含量和凋亡的变化情况,免疫组化SP法检测COX-2的表达情况。结果 塞来昔布对CNE-2细胞有明显的增殖抑制作用,呈时间和剂量依赖性。细胞周期各时相DNA 含量改变明显,G0~G1期细胞显著升高 (由最初47.03%升至最高79.20%),而S、G2M期细胞明显下降;凋亡率显著增高。塞来昔布明显下调细胞中COX-2蛋白的表达。结论 塞来昔布对鼻咽癌CNE-2 细胞有明显的增殖抑制作用,并且呈时间和剂量依赖性,使细胞聚集在G0/G1期,其机制涉及COX-2依赖性途径。

     

    Abstract: 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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