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用治疗性肽靶向恶性线粒体。

Targeting malignant mitochondria with therapeutic peptides.

作者信息

Constance Jonathan E, Lim Carol S

机构信息

Department of Pharmacology & Toxicology, College of Pharmacy, University of Utah, Salt Lake City, UT 84108, USA.

出版信息

Ther Deliv. 2012 Aug;3(8):961-79. doi: 10.4155/tde.12.75.

Abstract

The current status of peptides that target the mitochondria in the context of cancer is the focus of this review. Chemotherapy and radiotherapy used to kill tumor cells are principally mediated by the process of apoptosis that is governed by the mitochondria. The failure of anticancer therapy often resides at the level of the mitochondria. Therefore, the mitochondrion is a key pharmacological target in cancer due to many of the differences that arise between malignant and healthy cells at the level of this ubiquitous organelle. Additionally, targeting the characteristics of malignant mitochondira often rely on disruption of protein--protein interactions that are not generally amenable to small molecules. We discuss anticancer peptides that intersect with pathological changes in the mitochondrion.

摘要

本文综述聚焦于癌症背景下靶向线粒体的肽的现状。用于杀死肿瘤细胞的化疗和放疗主要通过线粒体调控的凋亡过程介导。抗癌治疗的失败往往发生在线粒体水平。因此,由于在这个普遍存在的细胞器水平上恶性细胞和健康细胞之间出现的许多差异,线粒体是癌症中的一个关键药理学靶点。此外,靶向恶性线粒体的特征通常依赖于破坏蛋白质 - 蛋白质相互作用,而这通常不适用于小分子。我们讨论了与线粒体病理变化相关的抗癌肽。

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