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机构地区:[1]浙江中医药大学附属第三医院,杭州310005 [2]军事医学科学院放射与辐射医学研究所,北京100850
出 处:《中国现代应用药学》2013年第12期1280-1285,共6页Chinese Journal of Modern Applied Pharmacy
基 金:国家自然科学基金资助项目(30572145;30970683);医院科研基金资助项目(ZS11ZA04)
摘 要:目的探讨选择性磷脂酰肌醇激酶相关蛋白激酶家族(PIKKs)的小分子抑制剂Wortmannnin对组蛋白去乙酰化酶抑制剂(HDIs)诱导的细胞凋亡的影响,并探讨DNA损伤功能信号级联在HDIs类药物抗肿瘤效应中的功能机制。方法流式细胞术分析加药后不同时间点的细胞周期分布和细胞凋亡情况;荧光显微镜下观察用药后的细胞核形态;免疫印迹法检测加药前后Caspase-2,Caspase-3,Caspase-7和Survivin蛋白表达情况。结果低剂量Wortmannin单独作用对肿瘤细胞生存率未见显著影响,但能够激活G1/S细胞周期阻滞、抑制TSA引发的G2/M阻滞、并显著促进肿瘤细胞凋亡。在此过程中,Wortmannin促进凋亡效应分子Caspase-2,Caspase-3和Caspase-7的激活并抑制Survivn的表达。结论 PIKKs家族的小分子抑制剂Wortmannnin通过下调Survivin并促进Caspase信号级联而促进TSA诱导的肿瘤细胞凋亡。OBJECTIVE To study the interaction between Wortmannnin, a selective inhibitor of PIKKs, and TSA, to explore the role of DNA damage signals in HDIs induced tumor cell death. METHODS The cell cycle distribution and cell apoptosis were detected by flow cytometry. The expression level of Caspase-2, 3, 7 and Survivin were determined by Western blotting with the antibody against each protein. RESULTS While low-dose Wortmannin alone had little effect on the tumor cell viability, it inhibited Trichostatin A (TSA) induced G2/M arrest and enhanced TSA induced apoptosis. TSA induced human acute lymphoblastic leukemia (MOLT-4) cells apoptosis through activation of Caspase-2, 3, 7. When pretreatment with Wortmannin, activation of Caspase-2, Caspase-3, and Caspase-7 by TSA was accelerated, and Survivin, a member of inhibitor of apoptosis protein (IAP) family, was also significantly decreased coincident with the acceleration of cells apoptosis. CONCLUSION As a PIKKs inhibitor, wortmannnin has been proposed as a potential anti-neoplastic agent. Wortmannin enhances TSA-induced tumor cells apoptosis through down-regulation of Survivin and activation of Caspase-cascades.
关 键 词:WORTMANNIN 组蛋白去乙酰化酶抑制剂 曲古抑菌素A 肿瘤 凋亡
分 类 号:R963[医药卫生—微生物与生化药学]
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