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TRAP1 调控肿瘤细胞中线粒体生死抉择及靶向 TRAP1 的抑制剂。

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

机构信息

Graduate Program of Life Science, School of Nano-Bioscience and Chemical Engineering, UNIST, Ulsan, Korea.

出版信息

BMB Rep. 2012 Jan;45(1):1-6. doi: 10.5483/bmbrep.2012.45.1.1.

Abstract

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 vitros and in vivo. In this review, recent developments in the study of mitochondrial chaperones and the mitochondria-targeted chaperone inhibitors are discussed.

摘要

热休克蛋白 90(Hsp90)是一种高度保守的分子伴侣,广泛存在于正常细胞中,在癌细胞中过度表达。研究发现,Hsp90 存在于癌细胞的线粒体中,许多癌症中也存在线粒体 Hsp90 同源物(TRAP1)的高表达。线粒体伴侣在调节线粒体完整性、抵御氧化应激和抑制细胞死亡方面发挥着重要作用。药理学失活伴侣可选择性诱导癌细胞线粒体功能障碍和细胞死亡,提示它们可能成为癌症治疗药物开发的靶蛋白。已经开发出几种针对线粒体中 TRAP1 和 Hsp90 的药物候选物,它们在许多癌症中表现出很强的细胞毒性活性,但在体外和体内的正常细胞中没有活性。本文讨论了近年来对线粒体伴侣和线粒体靶向伴侣抑制剂的研究进展。

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