Mitochondria: a target for cancer therapy

被引:203
作者
Armstrong, JS [1 ]
机构
[1] Natl Univ Singapore, Yong Loo Lin Sch Med, Fac Med, Dept Biochem, Singapore 117597, Singapore
关键词
mitochondria; apoptosis; Bcl-2; Bax; BH3; domain; cancer; mitochondrial membrane permeabilization; mitochondrial permeability transition; reactive oxygen species; cyclosporine A; mitochondrial membrane potential;
D O I
10.1038/sj.bjp.0706556
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Mitochondria, the cells powerhouses, are essential for maintaining cell life, and they also play a major role in regulating cell death, which occurs upon permeabilization of their membranes. Once mitochondrial membrane permeabilization (MMP) occurs, cells die either by apoptosis or necrosis. Key factors regulating MMP include calcium, the cellular redox status ( including levels of reactive oxygen species) and the mobilization and targeting to mitochondria of Bcl-2 family members. Contemporary approaches to targeting mitochondria in cancer therapy use strategies that either modulate the action of Bcl-2 family members at the mitochondrial outer membrane or use specific agents that target the mitochondrial inner membrane and the mitochondrial permeability transition (PT) pore. The aim of this review is to describe the major mechanisms regulating MMP and to discuss, with examples, mitochondrial targeting strategies for potential use in cancer therapy.
引用
收藏
页码:239 / 248
页数:10
相关论文
共 116 条
  • [91] Apoptosis: Programmed cell death at a molecular level
    Schultz, DR
    Harrington, WJ
    [J]. SEMINARS IN ARTHRITIS AND RHEUMATISM, 2003, 32 (06) : 345 - 369
  • [92] MULTIPLE BCL-2 FAMILY MEMBERS DEMONSTRATE SELECTIVE DIMERIZATIONS WITH BAX
    SEDLAK, TW
    OLTVAI, ZN
    YANG, E
    WANG, K
    BOISE, LH
    THOMPSON, CB
    KORSMEYER, SJ
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (17) : 7834 - 7838
  • [93] Mechanisms of caspase activation and inhibition during apoptosis
    Shi, YG
    [J]. MOLECULAR CELL, 2002, 9 (03) : 459 - 470
  • [94] Mitochondria in Ca2+ signaling and apoptosis
    Smaili, SS
    Hsu, YT
    Youle, RJ
    Russell, JT
    [J]. JOURNAL OF BIOENERGETICS AND BIOMEMBRANES, 2000, 32 (01) : 35 - 46
  • [95] STEINMAN HM, 1995, J BIOL CHEM, V270, P3487
  • [96] LONIDAMINE-INDUCED, PH DEPENDENT INHIBITION OF CELLULAR OXYGEN UTILIZATION
    STRYKER, JA
    GERWECK, LE
    [J]. RADIATION RESEARCH, 1988, 113 (02) : 356 - 361
  • [97] Molecular characterization of mitochondrial apoptosis-inducing factor
    Susin, SA
    Lorenzo, HK
    Zamzami, N
    Marzo, I
    Snow, BE
    Brothers, GM
    Mangion, J
    Jacotot, E
    Costantini, P
    Loeffler, M
    Larochette, N
    Goodlett, DR
    Aebersold, R
    Siderovski, DP
    Penninger, JM
    Kroemer, G
    [J]. NATURE, 1999, 397 (6718) : 441 - 446
  • [98] Bcl-2 inhibits the mitochondrial release of an apoptogenic protease
    Susin, SA
    Zamzami, N
    Castedo, M
    Hirsch, T
    Marchetti, P
    Macho, A
    Daugas, E
    Geuskens, M
    Kroemer, G
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 184 (04) : 1331 - 1341
  • [99] A serine protease, HtrA2, is released from the mitochondria and interacts with XIAP, inducing cell death
    Suzuki, Y
    Imai, Y
    Nakayama, H
    Takahashi, K
    Takio, K
    Takahashi, R
    [J]. MOLECULAR CELL, 2001, 8 (03) : 613 - 621
  • [100] AIF deficiency compromises oxidative phosphorylation
    Vahsen, N
    Candé, C
    Brière, JJ
    Bénit, P
    Joza, N
    Larochette, N
    Mastroberardino, PG
    Pequignot, MO
    Casares, N
    Lazar, V
    Feraud, O
    Debili, N
    Wissing, S
    Engelhardt, S
    Madeo, F
    Piacentini, M
    Penninger, JM
    Schägger, H
    Rustin, P
    Kroemer, G
    [J]. EMBO JOURNAL, 2004, 23 (23) : 4679 - 4689