Cell death decision by p53 via control of the mitochondrial membrane

被引:89
作者
Dashzeveg, Nurmaa [1 ]
Yoshida, Kiyotsugu [1 ]
机构
[1] Jikei Univ, Sch Med, Dept Biochem, Minato Ku, Tokyo 1058461, Japan
基金
日本学术振兴会;
关键词
p53; Mitochondria; Apoptosis; Necrosis; Necroptosis; TUMOR-SUPPRESSOR P53; DNA-BINDING DOMAIN; BCL-2; FAMILY; MULTIDRUG-RESISTANCE; TARGETING BCL2; IN-VITRO; BAX; APOPTOSIS; NECROSIS; PUMA;
D O I
10.1016/j.canlet.2015.07.019
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The tumor suppressor p53 is mutated in more than half of human cancers. Recent evidence has revealed that p53 not only regulates apoptosis but also regulates necrotic/necroptotic cell death via the mitochondria. The regulation of apoptosis by p53 is tightly connected to the mitochondrial outer membrane permeabilization and the induction of and interaction with Bcl-2 family members. Interestingly, p53-mediated regulation of necrosis/necroptosis is correlated with mitochondrial permeabilization pore opening via interactions with CypD and Drp1. This review discusses the p53-regulating molecules that induce apoptosis or necrosis/necroptosis via the mitochondria. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:108 / 112
页数:5
相关论文
共 61 条
  • [51] cIAP1 and TAK1 protect cells from TNF-induced necrosis by preventing RIP1/RIP3-dependent reactive oxygen species production
    Vanlangenakker, N.
    Vanden Berghe, T.
    Bogaert, P.
    Laukens, B.
    Zobel, K.
    Deshayes, K.
    Vucic, D.
    Fulda, S.
    Vandenabeele, P.
    Bertrand, M. J. M.
    [J]. CELL DEATH AND DIFFERENTIATION, 2011, 18 (04) : 656 - 665
  • [52] p53 Opens the Mitochondrial Permeability Transition Pore to Trigger Necrosis
    Vaseva, Angelina V.
    Marchenko, Natalie D.
    Ji, Kyungmin
    Tsirka, Stella E.
    Holzmann, Sonja
    Moll, Ute M.
    [J]. CELL, 2012, 149 (07) : 1536 - 1548
  • [53] miR-499 regulates mitochondrial dynamics by targeting calcineurin and dynamin-related protein-1
    Wang, Jian-Xun
    Jiao, Jian-Qin
    Li, Qian
    Long, Bo
    Wang, Kun
    Liu, Jin-Ping
    Li, Yan-Rui
    Li, Pei-Feng
    [J]. NATURE MEDICINE, 2011, 17 (01) : 71 - U243
  • [54] miR-34a, a microRNA up-regulated in a double transgenic mouse model of Alzheimer's disease, inhibits bcl2 translation
    Wang, Xiaoying
    Liu, Peng
    Zhu, Hua
    Xu, Yanfeng
    Ma, Chunmei
    Dai, Xiaowei
    Huang, Lan
    Liu, Yali
    Zhang, Lianfeng
    Qin, Chuan
    [J]. BRAIN RESEARCH BULLETIN, 2009, 80 (4-5) : 268 - 273
  • [55] The Mitochondrial Phosphatase PGAM5 Functions at the Convergence Point of Multiple Necrotic Death Pathways
    Wang, Zhigao
    Jiang, Hui
    Chen, She
    Du, Fenghe
    Wang, Xiaodong
    [J]. CELL, 2012, 148 (1-2) : 228 - 243
  • [56] Proapoptotic BAX and BAK: A requisite gateway to mitochondrial dysfunction and death
    Wei, MC
    Zong, WX
    Cheng, EHY
    Lindsten, T
    Panoutsakopoulou, V
    Ross, AJ
    Roth, KA
    MacCregor, GR
    Thompson, CB
    Korsmeyer, SJ
    [J]. SCIENCE, 2001, 292 (5517) : 727 - 730
  • [57] miR-15b and miR-16 modulate multidrug resistance by targeting BCL2 in human gastric cancer cells
    Xia, Lin
    Zhang, Dexin
    Du, Rui
    Pan, Yanglin
    Zhao, Lina
    Sun, Shiren
    Hong, Liu
    Liu, Jie
    Fan, Daiming
    [J]. INTERNATIONAL JOURNAL OF CANCER, 2008, 123 (02) : 372 - 379
  • [58] Xu K, 2011, MOL CARCINOG, V52, P70
  • [59] RAS-RAF-MEK-dependent oxidative cell death involving voltage-dependent anion channels
    Yagoda, Nicholas
    von Rechenberg, Moritz
    Zaganjor, Elma
    Bauer, Andras J.
    Yang, Wan Seok
    Fridman, Daniel J.
    Wolpaw, Adam J.
    Smukste, Inese
    Peltier, John M.
    Boniface, J. Jay
    Smith, Richard
    Lessnick, Stephen L.
    Sahasrabudhe, Sudhir
    Stockwell, Brent R.
    [J]. NATURE, 2007, 447 (7146) : 864 - 868
  • [60] miR-200bc/429 cluster modulates multidrug resistance of human cancer cell lines by targeting BCL2 and XIAP
    Zhu, Wei
    Xu, Huaguo
    Zhu, DanXia
    Zhi, Hui
    Wang, Tongshan
    Wang, Jian
    Jiang, Binghua
    Shu, Yongqian
    Liu, Ping
    [J]. CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2012, 69 (03) : 723 - 731