How does caspases regulation play role in cell decisions? apoptosis and beyond

被引:15
作者
Ghorbani, Negar [1 ]
Yaghubi, Roham [2 ]
Davoodi, Jamshid [1 ]
Pahlavan, Sara [3 ]
机构
[1] Univ Tehran, Inst Biochem & Biophys, Dept Biochem, Tehran, Iran
[2] Univ Tehran, Coll Sci, Dept Biotechnol, Tehran, Iran
[3] ACECR, Dept Stem Cells & Dev Biol, Royan Inst Stem Cell Biol & Technol, Cell Sci Res Ctr, Tehran, Iran
基金
美国国家科学基金会;
关键词
Caspases; Apoptosis; Caspase regulators; Apoptosis inhibition; Non-apoptotic function of caspases; LONG-TERM DEPRESSION; INHIBITORY SITE; CANCER-CELLS; PHOSPHORYLATION; ACTIVATION; PROTEIN; MECHANISM; ISOFORM; IDENTIFICATION; DEGRADATION;
D O I
10.1007/s11010-023-04870-5
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Caspases are a family of cysteine proteases, and the key factors behind the cellular events which occur during apoptosis and inflammation. However, increasing evidence shows the non-conventional pro-survival action of apoptotic caspases in crucial processes. These cellular events include cell proliferation, differentiation, and migration, which may appear in the form of metastasis, and chemotherapy resistance in cancerous situations. Therefore, there should be a precise and strict control of caspases activity, perhaps through maintaining the threshold below the required levels for apoptosis. Thus, understanding the regulators of caspase activities that render apoptotic caspases as non-apoptotic is of paramount importance both mechanistically and clinically. Furthermore, the functions of apoptotic caspases are affected by numerous post-translational modifications. In the present mini-review, we highlight the various mechanisms that directly impact caspases with respect to their anti- or non-apoptotic functions. In this regard, post-translational modifications (PTMs), isoforms, subcellular localization, transient activity, substrate availability, substrate selection, and interaction-mediated regulations are discussed.
引用
收藏
页码:1599 / 1613
页数:15
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