Mitochondrially targeted anti-cancer agents

被引:108
作者
Biasutto, Lucia [2 ]
Dong, Lan-Feng [3 ]
Zoratti, Mario [1 ,2 ]
Neuzil, Jiri [3 ,4 ]
机构
[1] Univ Padua, Dept Biomed Sci, CNR, Inst Neurosci, I-35121 Padua, Italy
[2] Univ Padua, Dept Expt Biomed Sci, I-35121 Padua, Italy
[3] Griffith Univ, Sch Med Sci, Southport, Qld 4222, Australia
[4] Acad Sci Czech Republ, Inst Biotechnol, Prague, Czech Republic
基金
澳大利亚研究理事会;
关键词
Mitochondrial targeting; Anti cancer drugs; Pro oxidant effect; Reactive oxygen species; ADENINE-NUCLEOTIDE TRANSLOCATOR; PERMEABILITY TRANSITION PORE; ALPHA-TOCOPHERYL SUCCINATE; CYTOCHROME-C RELEASE; PERIPHERAL BENZODIAZEPINE-RECEPTOR; DEPENDENT ANION CHANNEL; VITAMIN-E ANALOGS; SENSITIVE FUSOGENIC PEPTIDE; 10-N-NONYL ACRIDINE-ORANGE; NONVIRAL GENE DELIVERY;
D O I
10.1016/j.mito.2010.06.004
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cancer is an ever-increasing problem that is yet to be harnessed Frequent mutations make this pathology very variable and consequently a considerable challenge Intriguingly mitochondria have recently emerged as novel targets for cancer therapy A group of agents with anti-cancer activity that induce apoptosis by way of mitochondrial destabilisation termed mitocans have been a recent focus of research Of these compounds many are hydrophobic agents that associate with various sub cellular organelles Clearly modification of such structures with mitochondria targeting moieties for example tagging them with lipophilic cations would be expected to enhance their activity This may be accomplished by the addition of triphenylphosphonium groups that direct such compounds to mitochondria enhancing their activity In this paper we will review agents that possess anti-cancer activity by way of destabilising mitochondria and their possible targets We propose that mitochondrial targeting in particular where the agent associates directly with the target results in more specific and efficient anti-cancer drugs of potential high clinical relevance (C) 2010 Elsevier BV and Mitochondria Research Society All rights reserved
引用
收藏
页码:670 / 681
页数:12
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