The therapeutic potential of targeting regulated non-apoptotic cell death

被引:196
作者
Hadian, Kamyar [1 ]
Stockwell, Brent R. R. [2 ,3 ]
机构
[1] Helmholtz Zentrum Munchen, Res Unit Signaling & Translat, Neuherberg, Germany
[2] Columbia Univ, Dept Biol Sci, New York, NY 10027 USA
[3] Columbia Univ, Dept Chem, New York, NY 10027 USA
关键词
MIXED LINEAGE KINASE; POLY(ADP-RIBOSE) PAR POLYMER; INTERACTING PROTEIN-1 RIP1; GLUTATHIONE-PEROXIDASE; 4; GAMMA-INDUCING FACTOR; HIGHLY POTENT; NLRP3; INFLAMMASOME; DOMAIN-LIKE; LIPID-PEROXIDATION; COGNITIVE IMPAIRMENT;
D O I
10.1038/s41573-023-00749-8
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Several forms of non-apoptotic cell death, such as necroptosis, pyroptosis, parthanatos and ferroptosis, are implicated in degenerative diseases, cancer and inflammation. This article describes the molecular pathways regulating these forms of cell death and gives an update on small-molecule inhibitors being developed to target these pathways. Cell death is critical for the development and homeostasis of almost all multicellular organisms. Moreover, its dysregulation leads to diverse disease states. Historically, apoptosis was thought to be the major regulated cell death pathway, whereas necrosis was considered to be an unregulated form of cell death. However, research in recent decades has uncovered several forms of regulated necrosis that are implicated in degenerative diseases, inflammatory conditions and cancer. The growing insight into these regulated, non-apoptotic cell death pathways has opened new avenues for therapeutic targeting. Here, we describe the regulatory pathways of necroptosis, pyroptosis, parthanatos, ferroptosis, cuproptosis, lysozincrosis and disulfidptosis. We discuss small-molecule inhibitors of the pathways and prospects for future drug discovery. Together, the complex mechanisms governing these pathways offer strategies to develop therapeutics that control non-apoptotic cell death.
引用
收藏
页码:723 / 742
页数:20
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