Mitochondria-targeted vitamin E analogs inhibit breast cancer cell energy metabolism and promote cell death.

ABSTRACT:

Background

Recent research has revealed that targeting mitochondrial bioenergetic metabolism is a promising chemotherapeutic strategy. Key to successful implementation of this chemotherapeutic strategy is the use of new and improved mitochondria-targeted cationic agents that selectively inhibit energy metabolism in breast cancer cells, while exerting little or no long-term cytotoxic effect in normal cells.

Methods

In this study, we investigated the cytotoxicity and alterations in bioenergetic metabolism induced by mitochondria-targeted vitamin E analog (Mito-chromanol, Mito-ChM) and its acetylated ester analog (Mito-ChMAc). Assays of cell death, colony formation, mitochondrial bioenergetic function, intracellular ATP levels, intracellular and tissue concentrations of tested

SUBMITTER: Cheng G 

PROVIDER: S-EPMC3686663 | biostudies-literature | 2013 Jun

REPOSITORIES: biostudies-literature