TRAP1 regulation of mitochondrial life or death decision in cancer cells and mitochondria-targeted TRAP1 inhibitors

被引:60
|
作者
Kang, Byoung Heon [1 ,2 ]
机构
[1] UNIST, Grad Program Life Sci, Sch Nanobiosci & Chem Engn, Ulsan 689798, South Korea
[2] UNIST, Sci Res Ctr C5, Ulsan 689798, South Korea
基金
新加坡国家研究基金会;
关键词
Anticancer drugs; Cyclophlin D; Gamitrinibs; Hsp90; Mitochondria; Molecular chaperones; TRAP1; NECROSIS-FACTOR RECEPTOR; PERMEABILITY TRANSITION PORE; CYCLOPHILIN-D; HEAT-SHOCK; HSP90; INHIBITORS; OXIDATIVE STRESS; MOLECULAR CHAPERONES; PROTEIN-1; TRAP1; PROSTATE-CANCER; PROTECTS CELLS;
D O I
10.5483/BMBRep.2012.45.1.1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hsp90 is one of the most conserved molecular chaperones ubiquitously expressed in normal cells and over-expressed in cancer cells. A pool of Hsp90 was found in cancer mitochondria and the expression of the mitochondrial Hsp90 homolog, TRAP1, was also elevated in many cancers. The mitochondrial pool of chaperones plays important roles in regulating mitochondrial integrity, protecting against oxidative stress, and inhibiting cell death. Pharmacological inactivation of the chaperones induced mitochondrial dysfunction and concomitant cell death selectively in cancer cells, suggesting they can be target proteins for the development of cancer therapeutics. Several drug candidates targeting TRAP1 and Hsp90 in the mitochondria have been developed and have shown strong cytotoxic activity in many cancers, but not in normal cells in vitro and in vivo. In this review, recent developments in the study of mitochondrial chaperones and the mitochondria-targeted chaperone inhibitors are discussed [BMB reports 2012; 45(1): 1-6]
引用
收藏
页码:1 / 6
页数:6
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