Overcoming Drug Resistance by Targeting Cancer Bioenergetics with an Activatable Prodrug

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WEB OF SCIENCE

95
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99

초록

Nearly without exception, all known cancer chemotherapeutics elicit a resistance response over time. The resulting resistance is correlated with poor clinical outcomes. Here, we report an approach to overcoming resistance through reprogramming oncogene-directed alterations in mitochondrial metabolism before drug activation while simultaneously circumventing drug efflux pumps. Conjugate Cl increases cancer cell apoptosis and inhibits regrowth of drug-resistant tumors, as inferred from efficacy studies carried out in human cancer cells and in Dox-resistant xenograft tumor models. It also displays minimal whole-animal toxicity. These benefits are ascribed to an ability to evade chemo-resistance by switching cancer cell metabolism back to normal mitochondrial oxidative phosphorylation while helping target the active Dox to first the mito-chondrion and then the nucleus.

키워드

bioenergetics; cancer metabolism; carboxylesterase; dichloroacetic acid; doxorubicin; multidrug resistance; prodrug; SDG3: Good health and well-being; targeted therapeutics; Warburg effect; MULTIDRUG-RESISTANCE; METABOLIC REQUIREMENTS; IN-VIVO; DELIVERY; CELLS; MECHANISMS; DOXORUBICIN; GLYCOLYSIS; STRATEGY; RELEASE
제목
Overcoming Drug Resistance by Targeting Cancer Bioenergetics with an Activatable Prodrug
저자
Sharma, Amit; Lee, Min-Goo; Shi, Hu; Won, Miae; Arambula, Jonathan F.; Sessler, Jonathan L.; Lee, Jin Yong; Chi, Sung-Gil; Kim, Jong Seung
DOI
10.1016/j.chempr.2018.08.002
발행일
2018-10-11
유형
Article
저널명
Chem
권
4
호
10
페이지
2370 ~ 2383