ATP结合盒运输机
Abcg2型
ABCC1公司
运输机
多重耐药
流出
生物
多药耐药蛋白2
P-糖蛋白
癌症
抗药性
计算生物学
药理学
生物信息学
医学
基因
遗传学
作者
Akina Tamaki,Caterina Ieranò,Gergely Szakács,Robert W. Robey,Susan E. Bates
出处
期刊:Essays in Biochemistry
[Portland Press]
日期:2011-09-07
卷期号:50: 209-232
被引量:192
摘要
The phenomenon of multidrug resistance in cancer is often associated with the overexpression of the ABC (ATP-binding cassette) transporters Pgp (P-glycoprotein) (ABCB1), MRP1 (multidrug resistance-associated protein 1) (ABCC1) and ABCG2 [BCRP (breast cancer resistance protein)]. Since the discovery of Pgp over 35 years ago, studies have convincingly linked ABC transporter expression to poor outcome in several cancer types, leading to the development of transporter inhibitors. Three generations of inhibitors later, we are still no closer to validating the 'Pgp hypothesis', the idea that increased chemotherapy efficacy can be achieved by inhibition of transporter-mediated efflux. In this chapter, we highlight the difficulties and past failures encountered in the development of clinical inhibitors of ABC transporters. We discuss the challenges that remain in our effort to exploit decades of work on ABC transporters in oncology. In learning from past mistakes, it is hoped that ABC transporters can be developed as targets for clinical intervention.
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