坏死性下垂
自噬
程序性细胞死亡
串扰
癌细胞
小分子
癌症
化学
细胞凋亡
癌症治疗
癌症研究
细胞生物学
生物
生物化学
遗传学
物理
光学
作者
Junhao Wu,Jing Ye,Qiang Xie,Bo Liu,Ming Liu
标识
DOI:10.1021/acs.jmedchem.1c01572
摘要
Regulated cell death is a widely attractive subject among the topics of cancer therapy and has gained some advances for discovery of targeted anticancer drugs. In the past decade, nonapoptotic regulated cell death has been implicated in the development and therapeutic responses of a variety of human cancers. Hitherto, targeting autophagy-dependent cell death (ADCD), ferroptosis, and necroptosis with small molecules has been emerging as a hopeful strategy for the improvement of potential cancer therapy, which may have an advantage to bypass the apoptosis-resistance machinery. Thus, in this perspective, we concentrate on the key molecular insights into ADCD, ferroptosis, and necroptosis and summarize the corresponding small molecules in potential cancer therapy. Moreover, the relationships between the three subroutines and small molecules modulating the crosstalk are discussed. We believe that these inspiring findings would be advantageous to exploiting more potential targets and pharmacological small molecules in future cancer treatment.
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