MRP1 and its role in anticancer drug resistance

被引:125
|
作者
Lu, Jamie F. [1 ]
Pokharel, Deep [1 ]
Bebawy, Mary [1 ]
机构
[1] Univ Technol Sydney, Discipline Pharm, Grad Sch Hlth, Sydney, NSW 2007, Australia
基金
英国医学研究理事会;
关键词
Microparticles; multidrug resistance; multidrug resistance-associated protein 1; intercellular transfer; P-glycoprotein; trait dominance; cancer; CELL LUNG-CANCER; PROTEINS P-GLYCOPROTEIN; SOFT-TISSUE SARCOMAS; MULTIDRUG-RESISTANCE; BREAST-CANCER; ATP-BINDING; ABC TRANSPORTERS; GENE-EXPRESSION; LEUKEMIA-CELLS; NEOADJUVANT CHEMOTHERAPY;
D O I
10.3109/03602532.2015.1105253
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The phenomenon of multidrug resistance (MDR) in cancer is associated with the overexpression of the ATP-binding cassette (ABC) transporter proteins, including multidrug resistance-associated protein 1 (MRP1) and P-glycoprotein. MRP1 plays an active role in protecting cells by its ability to efflux a vast array of drugs to sub-lethal levels. There has been much effort in elucidating the mechanisms of action, structure and substrates and substrate binding sites of MRP1 in the last decade. In this review, we detail our current understanding of MRP1, its clinical relevance and highlight the current environment in the search for MRP1 inhibitors. We also look at the capacity for the rapid intercellular transfer of MRP1 phenotype from spontaneously shed membrane vesicles known as microparticles and discuss the clinical and therapeutic significance of this in the context of cancer MDR.
引用
收藏
页码:406 / 419
页数:14
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