The intersection between cysteine proteases, Ca2+signalling and cancer cell apoptosis*

被引:4
|
作者
Hua, Trinh [1 ]
Robitaille, Melanie [1 ]
Roberts-Thomson, Sarah J. [1 ]
Monteith, Gregory R. [1 ,2 ]
机构
[1] Univ Queensland, Sch Pharm, Brisbane, Qld 4102, Australia
[2] Univ Queensland, Mater Res Inst, Translat Res Inst, Brisbane, Qld, Australia
来源
基金
英国医学研究理事会;
关键词
Apoptosis; Calcium; Caspase; Calpain; Cathepsin; Cancer; INOSITOL 1,4,5-TRISPHOSPHATE RECEPTOR; MITOCHONDRIAL CALCIUM UNIPORTER; EPIDERMAL-GROWTH-FACTOR; CYTOCHROME-C RELEASE; M-CALPAIN ACTIVATION; CATHEPSIN-B; ENDOPLASMIC-RETICULUM; MU-CALPAIN; INTRACELLULAR CA2+; DOWN-REGULATION;
D O I
10.1016/j.bbamcr.2023.119532
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Apoptosis is a highly complex and regulated cell death pathway that safeguards the physiological balance between life and death. Over the past decade, the role of Ca2+ signalling in apoptosis and the mechanisms involved have become clearer. The initiation and execution of apoptosis is coordinated by three distinct groups of cysteines proteases: the caspase, calpain and cathepsin families. Beyond its physiological importance, the ability to evade apoptosis is a prominent hallmark of cancer cells. In this review, we will explore the involvement of Ca2+ in the regulation of caspase, calpain and cathepsin activity, and how the actions of these cysteine proteases alter intracellular Ca2+ handling during apoptosis. We will also explore how apoptosis resistance can be achieved in cancer cells through deregulation of cysteine proteases and remodelling of the Ca2+ signalling toolkit.
引用
收藏
页数:13
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