Targeting apoptotic caspases in cancer

被引:336
作者
Boice, Ashley [1 ,2 ,3 ]
Bouchier-Hayes, Lisa [1 ,2 ,3 ]
机构
[1] Baylor Coll Med, Dept Pediat, Div Hematol Oncol, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Mol & Cellular Biol, Houston, TX 77030 USA
[3] Texas Childrens Hosp, William T Shearer Ctr Human Immunobiol, Houston, TX 77030 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2020年 / 1867卷 / 06期
基金
美国国家卫生研究院;
关键词
Caspase; Cancer; Apoptosis; IAPs; Mitochondria; KAPPA-B ACTIVATION; TRAIL-INDUCED APOPTOSIS; SMAC-MIMETIC BIRINAPANT; X-LINKED INHIBITOR; CELL-DEATH; CYTOCHROME-C; SIGNALING COMPLEX; STRUCTURAL BASIS; CRYSTAL-STRUCTURE; BREAST-CANCER;
D O I
10.1016/j.bbamcr.2020.118688
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Members of the caspase family of proteases play essential roles in the initiation and execution of apoptosis. These caspases are divided into two groups: the initiator caspases (caspase-2, -8, -9 and -10), which are the first to be activated in response to a signal, and the executioner caspases (caspase-3, -6, and -7) that carry out the demolition phase of apoptosis. Many conventional cancer therapies induce apoptosis to remove the cancer cell by engaging these caspases indirectly. Newer therapeutic applications have been designed, including those that specifically activate individual caspases using gene therapy approaches and small molecules that repress natural inhibitors of caspases already present in the cell. For such approaches to have maximal clinical efficacy, emerging insights into non-apoptotic roles of these caspases need to be considered. This review will discuss the roles of caspases as safeguards against cancer in the context of the advantages and potential limitations of targeting apoptotic caspases for the treatment of cancer.
引用
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页数:15
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共 210 条
[1]
Akt promotes chemoresistance in human ovarian cancer cells by modulating cisplatin-induced, p53-dependent ubiquitination of FLICE-like inhibitory protein [J].
Abedini, M. R. ;
Muller, E. J. ;
Bergeron, R. ;
Gray, D. A. ;
Tsang, B. K. .
ONCOGENE, 2010, 29 (01) :11-25
[2]
Cisplatin induces p53-dependent FLICE-like inhibitory protein ubiquitination in ovarian cancer cells [J].
Abedini, Mohammad R. ;
Muller, Emilie J. ;
Brun, Jan ;
Bergeron, Richard ;
Gray, Douglas A. ;
Tsang, Benjamin K. .
CANCER RESEARCH, 2008, 68 (12) :4511-4517
[3]
Regulation of apoptotic protease activating factor-1 oligomerization and apoptosis by the WD-40 repeat region [J].
Adrain, C ;
Slee, EA ;
Harte, MT ;
Martin, SJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (30) :20855-20860
[4]
Human ICE/CED-3 protease nomenclature [J].
Alnemri, ES ;
Livingston, DJ ;
Nicholson, DW ;
Salvesen, G ;
Thornberry, NA ;
Wong, WW ;
Yuan, JY .
CELL, 1996, 87 (02) :171-171
[5]
Genes of glycolysis are ubiquitously overexpressed in 24 cancer classes [J].
Altenberg, B ;
Greulich, KO .
GENOMICS, 2004, 84 (06) :1014-1020
[6]
A Phase I Study of the SMAC-Mimetic Birinapant in Adults with Refractory Solid Tumors or Lymphoma [J].
Amaravadi, Ravi K. ;
Schilder, Russell J. ;
Martin, Lainie P. ;
Levin, Myron ;
Graham, Martin A. ;
Weng, David E. ;
Adjei, Alex A. .
MOLECULAR CANCER THERAPEUTICS, 2015, 14 (11) :2569-2575
[7]
Bortezomib sensitizes non-small cell lung cancer to mesenchymal stromal cell-delivered inducible caspase-9-mediated cytotoxicity [J].
Ando, M. ;
Hoyos, V. ;
Yagyu, S. ;
Tao, W. ;
Ramos, C. A. ;
Dotti, G. ;
Brenner, M. K. ;
Bouchier-Hayes, L. .
CANCER GENE THERAPY, 2014, 21 (11) :472-482
[8]
Phagocytosis of apoptotic cells in homeostasis [J].
Arandjelovic, Sanja ;
Ravichandran, Kodi S. .
NATURE IMMUNOLOGY, 2015, 16 (09) :907-917
[9]
The biochemical mechanism of caspase-2 activation [J].
Baliga, BC ;
Read, SH ;
Kumar, S .
CELL DEATH AND DIFFERENTIATION, 2004, 11 (11) :1234-1241
[10]
The crystal structure of caspase-6, a selective effector of axonal degeneration [J].
Baumgartner, Renato ;
Meder, Gabriele ;
Briand, Christophe ;
Decock, Arnaud ;
D'Arcy, Allan ;
Hassiepen, Ulrich ;
Morse, Richard ;
Renatus, Martin .
BIOCHEMICAL JOURNAL, 2009, 423 :429-439