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首页> 外文期刊>Cell death & disease. >Artesunate induces necrotic cell death in schwannoma cells
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Artesunate induces necrotic cell death in schwannoma cells

机译:青蒿琥酯诱导神经鞘瘤细胞坏死细胞死亡

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摘要

Established as a potent anti-malaria medicine, artemisinin-based drugs have been suggested to have anti-tumour activity in some cancers. Although the mechanism is poorly understood, it has been suggested that artemisinin induces apoptotic cell death. Here, we show that the artemisinin analogue artesunate (ART) effectively induces cell death in RT4 schwannoma cells and human primary schwannoma cells. Interestingly, our data indicate for first time that the cell death induced by ART is largely dependent on necroptosis. ART appears to inhibit autophagy, which may also contribute to the cell death. Our data in human schwannoma cells show that ART can be combined with the autophagy inhibitor chloroquine (CQ) to potentiate the cell death. Thus, this study suggests that artemisinin-based drugs may be used in certain tumours where cells are necroptosis competent, and the drugs may act in synergy with apoptosis inducers or autophagy inhibitors to enhance their anti-tumour activity.
机译:作为一种有效的抗疟药,青蒿素类药物被建议在某些癌症中具有抗肿瘤活性。尽管对该机理了解甚少,但已表明青蒿素诱导凋亡细胞死亡。在这里,我们显示青蒿素类似物青蒿琥酯(ART)有效诱导RT4神经鞘瘤细胞和人类原发性神经鞘瘤细胞的细胞死亡。有趣的是,我们的数据首次表明ART诱导的细胞死亡在很大程度上取决于尸检。 ART似乎抑制自噬,这也可能导致细胞死亡。我们在人类神经鞘瘤细胞中的数据表明,ART可以与自噬抑制剂氯喹(CQ)结合以增强细胞死亡。因此,这项研究表明基于青蒿素的药物可用于某些具有细胞坏死性功能的肿瘤,并且该药物可与细胞凋亡诱导剂或自噬抑制剂协同作用以增强其抗肿瘤活性。

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