上睑下垂
白血病
癌症研究
炎症体
生物
细胞凋亡
化学
细胞生物学
免疫学
程序性细胞死亡
遗传学
炎症
作者
Yuanming He,Shuoyi Jiang,Yao‐Li Cui,Jingpei Liang,Yueya Zhong,Yuening Sun,Michael F. Moran,Zhigang Huang,Guisong He,Xinliang Mao
标识
DOI:10.1016/j.canlet.2024.216797
摘要
Induction of pyroptosis is proposed as a promising strategy for the treatment of hematological malignancies, but little is known. In the present study, we find clioquinol (CLQ), an anti-parasitic drug, induces striking myeloma and leukemia cell pyroptosis on a drug screen. RNA sequencing reveals that the interferon-inducible genes IFIT1 and IFIT3 are markedly upregulated and are essential for CLQ-induced GSDME activation and cell pyroptosis. Specifically, IFIT1 and IFIT3 form a complex with BAX and N-GSDME therefore directing N-GSDME translocalization to mitochondria and increasing mitochondrial membrane permeabilization and triggering pyroptosis. Furthermore, venetoclax, an activator of BAX and an inhibitor of Bcl-2, displays strikingly synergistic effects with CLQ against leukemia and myeloma via pyroptosis. This study thus reveals a novel mechanism for mitochondrial GSDME in pyroptosis and it also illustrates that induction of IFIT1/T3 and inhibition of Bcl-2 orchestrate the treatment of leukemia and myeloma via pyroptosis.
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