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机构地区:[1]延安大学医学院生理学教研室,陕西延安716000 [2]延安大学医学院免疫学教研室,陕西延安716000
出 处:《现代肿瘤医学》2009年第8期1423-1425,共3页Journal of Modern Oncology
基 金:陕西省教育厅专项科研基金(07jk429)
摘 要:目的:探讨环氧合酶-2(COX-2)特异性抑制剂SC236诱导胃癌细胞株SGC7901凋亡的机制。方法:SC236对人胃癌来源的SGC7901细胞进行凋亡诱导。以吖啶橙染色后荧光显微镜下观察凋亡细胞形态并计算凋亡指数。Western blot法检测凋亡调节蛋白Bcl-2、Bak、Bax与CED-9的表达情况。流式细胞仪检测细胞凋亡率。结果:SGC7901细胞经SC236作用后,细胞中凋亡促进因子Bak的表达水平明显增高、凋亡抑制因子Bcl-2的表达水平显著下降、而凋亡促进因子Bax和凋亡抑制因子CED-9表达水平无明显变化。细胞凋亡指数或凋亡率则随SC236浓度的增加和作用的时间延长而升高。结论:COX-2特异抑制剂SC236可通过上调凋亡促进因子Bak表达和下调凋亡抑制因子Bcl-2表达而诱导胃癌细胞株SGC7901的凋亡。Objective: To investigate the mechanism of apoptosis inducing effect of specific COX -2 inhibitor SC236 in gastric cancer cell line SGC7901. Methods: The expression level of apoptosis -regulating proteins Bcl - 2, Bak, Bax and CED -9 was analyzed by Western blot method. Cell apoptosis index was measured by fluorescence microscopy as well as by flow cytometry. Results: Treatment of SGC7901 gastric cancer cells with SC236 caused a significant elevation of the expression of the apoptosis - promoting proteins Bak and Bax, but a significant reduction of the expression of the apoptosis - inhibiting protein Bcl - 2 and CED - 9 were observed. Cell apoptosis index or rate increased with the increment of SC236 concentration and the time of action. Conclusion : Specific COX - 2 inhibitor SC236 could induce apoptosis in gastric cancer cell line SGC7901 through the up - regulation of the apoptosis - prorooting proteins Bak and Bax, and the down - regulation of the apoptosis - inhibiting protein Bcl - 2 and CED - 9.
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