Reversing agents for ATP-binding cassette (ABC) transporters: application in modulating multidrug resistance (MDR).

Chow H Lee
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引用次数: 53

Abstract

One of the main reasons for the failure in cancer chemotherapy is the existence of multidrug resistance (MDR) mechanisms. One form of MDR phenotype is contributed by a group of plasma membrane proteins that belong to a large superfamily of proteins called the ATP-binding cassette (ABC) transporters. There has been intense search for compounds, which can act at reversing MDR phenotype exhibited by ABC transporters such as P-glycoprotein (P-gp), multidrug-resistance protein (MRP) and breast cancer resistance protein (BCRP). Reversing agents can be designed to target MDR-associated ABC transporters at three levels - the protein, mRNA or DNA level. This review aims at describing, over-viewing and discussing currently known MDR reversing agents, which have been shown to act at either of the three levels against ABC transporters. Other potential agents and strategies, which can be used to reverse the MDR phenotype, are also discussed.

atp结合盒转运体逆转剂:在调节多药耐药(MDR)中的应用。
肿瘤化疗失败的主要原因之一是多药耐药机制的存在。一种形式的耐多药表型是由一组质膜蛋白贡献的,这些蛋白属于一个被称为atp结合盒(ABC)转运蛋白的大超家族。人们一直在努力寻找能够逆转ABC转运蛋白如p -糖蛋白(P-gp)、多药耐药蛋白(MRP)和乳腺癌耐药蛋白(BCRP)所表现出的耐多药表型的化合物。逆转剂可以设计为靶向耐多药相关的ABC转运蛋白在三个水平-蛋白质,mRNA或DNA水平。本综述旨在描述、概述和讨论目前已知的MDR逆转剂,这些药物已被证明在三个水平上对ABC转运蛋白起作用。其他潜在的药物和策略,可用于逆转耐多药表型,也进行了讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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