Mitochondrial Drug Targets in Cell Death and Cancer

被引:33
作者
Ferrin, Gustavo [1 ]
Linares, Clara I. [1 ]
Muntane, Jordi [1 ]
机构
[1] Hosp Univ Reina Sofia, Liver Res Unit, IMIBIC, Inst Maimonides Invest Biomed Cordoba, E-14004 Cordoba, Spain
关键词
Apoptosis; metabolism; oxidative stress; therapy; HUMAN BREAST-CANCER; PERMEABILITY TRANSITION-PORE; ALPHA-TOCOPHERYL SUCCINATE; CYTOCHROME-C-OXIDASE; ACUTE PROMYELOCYTIC LEUKEMIA; ROTENONE-INDUCED APOPTOSIS; ACTIVATED PROTEIN-KINASE; SYNTHETIC RETINOID CD437; FATTY-ACID SYNTHASE; DIHYDROARTEMISININ INDUCES APOPTOSIS;
D O I
10.2174/138161211796904803
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Mitochondria are involved in different physiological and pathological processes that are crucial for tumor cell physiology, growth and survival. Since cancer cells have frequently disrupted different cell death pathways that promote their survival, mitochondria may be key organelles to promote cell death in cancer cells. The present review is focused on the different experimental and therapeutic cancer strategies addressed to either target mitochondria directly, or use mitochondria as mediators of apoptosis. While the first group includes drugs that act on glycolysis, beta-oxidation, electron transport chain, mitochondrial permeability and the Bcl-2/IAP family protein, the second one consists of those drugs that cause cell death through the intrinsic apoptosis pathway by promoting ROS generation or by modulating mitochondrial protein involved in apoptosis induction.
引用
收藏
页码:2002 / 2016
页数:15
相关论文
共 284 条
[1]
Imbalance of the mitochondrial pro- and anti-apoptotic mediators in neuroblastoma tumours with unfavourable biology [J].
Abel, F ;
Sjöberg, RM ;
Nilsson, S ;
Kogner, P ;
Martinsson, T .
EUROPEAN JOURNAL OF CANCER, 2005, 41 (04) :635-646
[2]
The Bcl-2 inhibitor ABT-263 enhances the response of multiple chemotherapeutic regimens in hematologic tumors in vivo [J].
Ackler, Scott ;
Mitten, Michael J. ;
Foster, Kelly ;
Oleksijew, Anatol ;
Refici, Marion ;
Tahir, Stephen K. ;
Xiao, Yu ;
Tse, Christin ;
Frost, David J. ;
Fesik, Stephen W. ;
Rosenberg, Saul H. ;
Elmore, Steven W. ;
Shoemaker, Alexander R. .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2010, 66 (05) :869-880
[3]
Interactions of ATP, oestradiol, genistein and the anti-olestrogens, faslodex (ICI 182780) and tamoxifen, with the human erythrocyte glucose transporter, GLUT1 [J].
Afzal, I ;
Cunningham, P ;
Naftalin, RJ .
BIOCHEMICAL JOURNAL, 2002, 365 (03) :707-719
[4]
BYPASSES OF THE ANTIMYCIN A BLOCK OF MITOCHONDRIAL ELECTRON-TRANSPORT IN RELATION TO UBISEMIQUINONE FUNCTION [J].
ALEXANDRE, A ;
LEHNINGER, AL .
BIOCHIMICA ET BIOPHYSICA ACTA, 1984, 767 (01) :120-129
[5]
3-NITROPROPIONATE, TOXIC SUBSTANCE OF INDIGOFERA, IS A SUICIDE INACTIVATOR OF SUCCINATE-DEHYDROGENASE - (RAT-LIVER MITOCHONDRIA CARBANION-N-5 FLAVIN ADDUCTS 2-PROTON ABSTRACTION MECHANISM) [J].
ALSTON, TA ;
MELA, L ;
BRIGHT, HJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1977, 74 (09) :3767-3771
[6]
Inhibition of β-oxidative respiration is a therapeutic window associated with the cancer chemo-preventive activity of PPARγ agonists [J].
Andela, VB ;
Altuwaijri, S ;
Wood, J ;
Rosier, RN .
FEBS LETTERS, 2005, 579 (07) :1765-1769
[7]
Paclitaxel targets mitochondria upstream of caspase activation in intact human neuroblastoma cells [J].
André, N ;
Carré, M ;
Brasseur, G ;
Pourroy, B ;
Kovacic, H ;
Briand, C ;
Braguer, D .
FEBS LETTERS, 2002, 532 (1-2) :256-260
[8]
Mitochondria: a target for cancer therapy [J].
Armstrong, JS .
BRITISH JOURNAL OF PHARMACOLOGY, 2006, 147 (03) :239-248
[9]
Rotenone-induced G2/M cell cycle arrest and apoptosis in a human B lymphoma cell line PW [J].
Armstrong, JS ;
Hornung, B ;
Lecane, P ;
Jones, DP ;
Knox, SJ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 289 (05) :973-978
[10]
DEPLETION OF MUSCLE MITOCHONDRIAL-DNA IN AIDS PATIENTS WITH ZIDOVUDINE-INDUCED MYOPATHY [J].
ARNAUDO, E ;
DALAKAS, M ;
SHANSKE, S ;
MORAES, CT ;
DIMAURO, S ;
SCHON, EA .
LANCET, 1991, 337 (8740) :508-510