髓系白血病
阿糖胞苷
癌症研究
白血病
细胞凋亡
造血
药理学
髓样
体内
生物
细胞毒性T细胞
化学
免疫学
干细胞
体外
细胞生物学
生物化学
生物技术
作者
Zhen Gao,Ze Long Cui,Min Ran Zhou,Yue Fu,Fen Liu,Lu Zhang,Sai Ma,Chun Yan Chen
标识
DOI:10.1016/j.bcp.2022.114948
摘要
Acute myeloid leukemia (AML) is a malignant proliferative disease of myeloid hematopoietic origin and cannot be treated appropriately at present. This is due to the fact that leukemia cells are not sensitive to some of the traditional chemotherapy drugs. Or some chemotherapeutic drugs are too toxic to normal cells, affecting their wide clinical application. In this study, we identified BAM15 as a novel mitochondrial uncoupling agent by screening a library of small molecule compounds that inhibit AML cell activity. BAM15 significantly inhibited proliferation and promoted apoptosis in AML cells while at the same time being less cytotoxic to normal cells. The mechanism may be related to the disturbance of the ROS production balance. In vivo investigations revealed that BAM15 effectively suppressed AML progression and prolonged the survival time of mice. In addition, we found that BAM15 can be used in combination with cytarabine to enhance its anti-cancer activity and inhibit the activity of primary cells in AML. Therefore, we identified BAM15 as a potential drug candidate for the treatment of AML.
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