Department of Physiology and Pharmacology, Chang Gung University, Tao-Yuan 333, Taiwan.
Mol Pharm. 2011 Dec 5;8(6):1996-2011. doi: 10.1021/mp200261n. Epub 2011 Jul 26.
Chemotherapy is currently one of the most effective ways to treat metastatic cancers. However, of the various mechanisms that are involved in conferring resistance, upregulation of drug efflux ATP-binding cassette (ABC) transporters, such as P-glycoprotein (ABCB1), multidrug resistance protein 1 (ABCC1) and ABCG2, has become a major obstacle to cancer chemotherapy and seriously affects the clinical outcome. To date, at least 15 ABC drug transporters have been identified and characterized to transport and confer resistance to practically the entire spectrum of cancer drugs, causing multidrug resistance (MDR) in cancers. Unfortunately, despite decades of research, there is still no real solution to MDR. This review highlights some of the major findings, the roles and problems associated with MDR-linked ABC drug transporters in metastatic cancers and solid tumors, and the current strategies to improve the clinical outcome in cancer chemotherapy.
化疗是目前治疗转移性癌症最有效的方法之一。然而,在赋予耐药性的各种机制中,药物外排 ATP 结合盒(ABC)转运蛋白的上调,如 P-糖蛋白(ABCB1)、多药耐药蛋白 1(ABCC1)和 ABCG2,已成为癌症化疗的主要障碍,严重影响临床疗效。迄今为止,已经鉴定和表征了至少 15 种 ABC 药物转运蛋白,它们能够转运并赋予几乎所有癌症药物的耐药性,导致癌症的多药耐药性(MDR)。不幸的是,尽管经过几十年的研究,仍然没有真正解决 MDR 的办法。这篇综述强调了一些主要的发现,以及与转移性癌症和实体瘤中与 MDR 相关的 ABC 药物转运体相关的作用和问题,以及改善癌症化疗临床疗效的当前策略。