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作 者:曹鹏[1] 梁勇[1] 范涤[1] 韩松[1] 于春泳[1] 冯思哲[1] 梁国标[1]
机构地区:[1]沈阳军区总医院神经外科,辽宁沈阳110016
出 处:《广州医学院学报》2012年第6期18-21,共4页Academic Journal of Guangzhou Medical College
摘 要:目的:探讨Notch通路特异性阻断药物MRK-560在体外抑制原代培养脑胶质瘤细胞增殖及诱导肿瘤细胞凋亡的能力。方法:选取24例脑胶质瘤标本进行原代分离以获取脑胶质瘤细胞,分别给予不同浓度的MRK-560共培养48 h,检测肿瘤细胞胞内γ-secretase活性、肿瘤细胞的增殖能力及肿瘤细胞的凋亡水平。结果:5~40μg/mL MRK-560可抑制脑胶质瘤细胞γ-secretase活性和脑胶质瘤细胞的增殖(P<0.05)。MRK-560共培养组与空白对照组凋亡率分别为(47.6±19.2)%与(6.3±4.2)%,两组比较,差异有统计学意义(P<0.01)。加入MRK-560后,Notch通路重要的效应分子NICD蛋白的表达被明显抑制。结论:Notch受体阻断剂MRK-560具有良好的体外抗肿瘤活性,在治疗脑胶质瘤方面具有非常重要的应用前景。Objective :To investigate the effects of MRK-560, a Notch signaling pathway specific inhibitor, on suppression of primary glioma cell proliferation and induction in vitro. Methods: The 24 glioma specimens were obtained for collection of cerebral glioma cells, which were subjected to primary culture with MRK-560 at different concentrations for 48 hours. The γ-seeretase activity, glioma cell proliferation and apoptosis were assayed. Results: MRK-560 at 5-40μg/mL inhibited the γ-secretase activity and glioma cell proliferation (both P 〈 0.05 ). Following co-culture with MRK-560, the apoptosis of glioma cells was substantially potentiated when compared with normal controls ( [ 47.6 ± 19.2 ] % vs. [ 6.3 ± 4. 2 ] %, P 〈 0.01 ). The addition of MRK-560 resuhed in marked attenuation of expression of N1CD, the selective effectors of Notch signaling pathway. Conclusion: MRK-560, a Notch signaling pathway inhibitor, is featured by potent anti-glioma effects in vitro and merits further studies for the treatment of cerebral glioma.
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