Double agents of cell death: novel emerging functions of apoptotic regulators

被引:16
|
作者
Lamb, Heather M. [1 ]
机构
[1] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, W Harry Feinstone Dept Mol Microbiol & Immunol, 615 N Wolfe St,Room W5104-1, Baltimore, MD 21205 USA
关键词
apoptosis; autophagy; BCL-2; cancer; caspase; ferroptosis; mPTP; necroptosis; pyroptosis; MITOCHONDRIAL PERMEABILITY TRANSITION; BCL-2 FAMILY PROTEINS; ENDOPLASMIC-RETICULUM; ATP SYNTHASE; MOLECULAR-MECHANISMS; BH3-ONLY PROTEINS; CANCER-THERAPY; SMAC MIMETICS; CYTOCHROME-C; AUTOPHAGY;
D O I
10.1111/febs.15308
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 regulated form of cell death that is required for many homeostatic and pathological processes. Recently, alternative cell death pathways have emerged whose regulation is dependent on proteins with canonical functions in apoptosis. Dysregulation of apoptotic signaling frequently underlies the pathogenesis of many cancers, reinforcing the need to develop therapies that initiate alternative cell death processes. This review outlines the convergence points between apoptosis and other death pathways with the purpose of identifying novel strategies for the treatment of apoptosis-refractory cancers. Apoptosis proteins can play key roles in the initiation, regulation, and execution of nonapoptotic death processes that include necroptosis, autophagy, pyroptosis, mPTP-mediated necrosis, and ferroptosis. Notably, recent evidence illustrates that dying cells can exhibit biochemical and molecular characteristics of more than one different type of regulated cell death. Thus, this review highlights the amazing complexity and interconnectivity of cell death processes and also raises the idea that a top-to-bottom approach to describing cell death mechanisms may be inadequate for fully understanding the means by which cells die.
引用
收藏
页码:2647 / 2663
页数:17
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