Cui Haigang, Zhang Anna J, Chen Mingwei, Liu Johnson J
School of Medicine, Faculty of Health, University of Tasmania. Private Bag 26 Hobart, Tasmania 7001 Australia.
Curr Drug Targets. 2015;16(12):1356-71. doi: 10.2174/1389450116666150330113506.
The superfamily of human ATP-binding cassette (ABC) transporters comprises seven subfamilies (ABCA to G) with 48 members. In addition to their profound physiological and pharmacological functions, ABC transporters play important roles in instigating multidrug resistance (MDR) in cancer by mediating the efflux of many anticancer drugs, particularly, ABCB1, ABCG2 and ABCC subfamily members. Previous development of ABCB1 transporter inhibitors has provided insights into seeking novel strategies in developing new classes of compound that inhibit ABCB1 and other MDRrelated ABC transporters. We herein review and evaluate current evidence in this area, with an emphasis on experimental and investigational agents that are under preclinical and clinical tests, including tyrosine kinase inhibitors, natural products, microRNAs and novel chemical entities. New strategies targeting ABC transporters in cancer stem cells and future perspectives in this field are also discussed.
人类ATP结合盒(ABC)转运蛋白超家族由7个亚家族(ABCA至G)组成,共有48个成员。ABC转运蛋白除了具有重要的生理和药理功能外,还通过介导许多抗癌药物的外排,在引发癌症多药耐药(MDR)中发挥重要作用,特别是ABCB1、ABCG2和ABCC亚家族成员。先前ABCB1转运蛋白抑制剂的开发为寻求开发抑制ABCB1和其他与MDR相关的ABC转运蛋白的新型化合物的新策略提供了思路。我们在此回顾和评估该领域的现有证据,重点关注正在进行临床前和临床试验的实验性和研究性药物,包括酪氨酸激酶抑制剂、天然产物、微小RNA和新型化学实体。还讨论了针对癌症干细胞中ABC转运蛋白的新策略以及该领域的未来前景。