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Effect of artesunate on inhibiting proliferation and inducing apoptosis of SP2/0 myeloma cells through affecting NFκB p65

机译:青蒿琥酯通过影响NFκBp65抑制SP2 / 0骨髓瘤细胞增殖并诱导其凋亡

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The initial treatment of multiple myeloma (MM) experienced a paradigm shift, in the past decade, with the introduction of novel agents such as thalidomide, lenalidomide and bortezomib, leading to improved outcomes. High dose therapy and autologous stem cell transplantation remain an important therapeutic option for patients with MM eligible for the procedure. However, most of these treatment regimens are too expensive for Chinese patients. Therefore, we investigated the effects of artesunate, which is commonly used in the treatment of severe malaria, on inhibition of proliferation and induction of apoptosis of a mouse myeloma cell line SP2/0. The growth inhibition of SP2/0 cell proliferation induced by artesunate (ART) treatment was measured using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) method and the rate of apoptosis and cell cycle changes induced by ART were analyzed by flow cytometry. ART-induced morphology changes of apoptosis in SP2/0 cells, as observed by light and transmission electron microscopy. Additionally, DNA laddering, which is a hallmark of apoptosis, was observed by agarose gel electrophoresis of DNA harvested from SP2/0 cells treated with ART. The levels of nuclear factor kappa B p65 (NFκB p65) protein in nucleus and the inhibitor of NFκB (IκBα) in the cytoplasm were measured by western blot analysis and ELISA to evaluate NFκB p65 transcription activity indirectly. The results show that artesunate inhibited the proliferation and induced apoptosis of SP2/0 cells in a dose- and time-dependent manner. Artesunate also increased the proportion of SP2/0 cells in G0/G1 phase, while decreased the proportion of cells in G2/M or S phase. Additionally, artesunate treatment decreased the level of NFκB p65 protein in the nucleus, while increased the level of IκBα protein in the cytoplasm. The present result is the first report to show that artesunate may be useful in the treatment of MM.
机译:在过去的十年中,随着沙利度胺,来那度胺和硼替佐米等新型药物的引入,多发性骨髓瘤(MM)的初始治疗发生了范式转变,从而改善了预后。高剂量疗法和自体干细胞移植仍然是符合该程序的MM患者的重要治疗选择。但是,这些治疗方案中的大多数对于中国患者来说太昂贵了。因此,我们研究了青蒿琥酯(通常用于治疗严重疟疾)对小鼠骨髓瘤细胞SP2 / 0的增殖抑制和凋亡诱导的影响。使用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴化物(MTT)方法测量青蒿琥酯(ART)诱导的SP2 / 0细胞增殖的生长抑制作用以及凋亡率和细胞用流式细胞仪分析了ART诱导的周期变化。如通过光和透射电子显微镜观察到的,ART诱导的SP2 / 0细胞凋亡的形态学变化。另外,通过从ART处理的SP2 / 0细胞中收获的DNA的琼脂糖凝胶电泳观察到DNA梯化是细胞凋亡的标志。通过western blot分析和ELISA法检测细胞核中的核因子κBp65(NFκBp65)蛋白和细胞质中NFκB(IκBα)抑制剂的水平,间接评估NFκBp65的转录活性。结果显示青蒿琥酯以剂量和时间依赖性方式抑制SP2 / 0细胞的增殖并诱导其凋亡。青蒿琥酯还增加了G 0 / G 1 期中SP2 / 0细胞的比例,同时降低了G2 / M或S期中SP2 / 0细胞的比例。此外,青蒿琥酯处理降低了细胞核中NFκBp65蛋白的水平,同时增加了细胞质中IκBα蛋白的水平。本结果是第一个报告,表明青蒿琥酯可能在MM的治疗中有用。

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