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作 者:杨珉[1] 蔡曙州[1] 魏俊[1] 王威[1] 董伟[1] 饶辉[1] 涂珍[2] 杨明[3] 王汉平[1] 彭付学[1] 何贵山[1]
机构地区:[1]孝感市中心医院神经外科 [2]孝感市中心医院病理科 [3]孝感市中心医院放射科
出 处:《中国临床神经外科杂志》2012年第2期97-99,共3页Chinese Journal of Clinical Neurosurgery
基 金:湖北省卫生厅2008年度青年科技人才基金项目(NO:QJX2008-57)
摘 要:目的研究内皮抑素对阿霉素(ADM)诱导的大鼠胶质瘤多药耐药细胞株GL15(GL15/ADM)细胞磷酸糖蛋白(P-gp)表达的抑制作用,探讨其对胶质瘤肿瘤耐药的影响。方法将内皮抑素质粒转染胶质瘤耐药细胞,应用免疫印迹法、荧光分光光度计和流式细胞术分别检测转染后6,12,24,48h不同时间段P-gp表达水平及天冬氨酸特异性半胱氨酸蛋白酶3(caspase-3)的活性和细胞凋亡率。结果转染后6h即可发现P-gp表达水平活性明显降低(P<0.05),且随转染后时间的延长而递减;转染后6h即可发现caspase-3活性明显上升(P<0.05),且随时间的延长而递增;转染后6、12、24、48h肿瘤细胞凋亡率上升,并与非转染组间有极显著性差异(P<0.01)。结论内皮抑素能通过上调Caspase-3的活性,明显抑制胶质瘤耐药细胞中P-gp表达水平和促进肿瘤细胞凋亡,有助于提高胶质瘤的综合治疗效果。Objective To investigate the effect of endostatin on the expression of phosphoglucoprotein ^(p-gp) in adriamycin (ADM)- induced multidrug resistance glioma cell line GL15 (GL15/ADM) cells in order to explore the role of endostatin in the glioma '.~ muhidrug resistance, iMethods The plasmids with endostatin (pcDNA 3.1 ES) were transfected into GL15/ADM cell, in which the expression of P-gp, the activity of cysteine-containing aspartate-specific proteases 3 (caspase-3) and the apoptosis were determined respectively by western blot, spectrofluorometer and flow cytometer 6, 12, 24, and 48 hours after the transfeetion. Results The signifuicnat decrease in the level of P-gp expression in GL15/ADM cells was observed 6 hours after the transfectton and it was positively related to the time after the transfection (P〈0.05). The signifuicnat increase in the activity of caspase-3 in~ GL15/ADM cells was observed 6 hours after the transfection and it was positively related to the time after the transfection (P〈0.05~). The apoptosis rates in GL15/ADM cells transfected into by pcDNA 3.1 ES were significance higher 6, !2, 24 and 48 hours after the transfection than those in the untransfected GLIS/ADM cells (P〈0.01). Conclusions Endostatin can inhibit the level of P-gp expression and promote the apoptosis in GL15/ADM cells by upregulation of the activity of caspase-3, and therefore it is helpful to the increase in the effect of comprehensive treatment on the gliomas.
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