Mammalian drug efflux transporters of the ATP binding cassette (ABC) family in multidrug resistance: A review of the past decade

被引:817
作者
Chen, Zhaolin [1 ,2 ]
Shi, Tianlu [1 ,2 ]
Zhang, Lei [1 ]
Zhu, Pengli [1 ]
Deng, Mingying [1 ]
Huang, Cheng [2 ]
Hu, Tingting [2 ]
Jiang, Ling [1 ]
Li, Jun [2 ]
机构
[1] Anhui Prov Hosp, Dept Pharm, Hefei 230001, Anhui, Peoples R China
[2] Anhui Med Univ, Inst Liver Dis, Anhui Inst Innovat Drugs, Anhui Key Lab Bioact Nat Prod,Sch Pharm, Hefei 230032, Anhui, Peoples R China
基金
美国国家科学基金会;
关键词
Multidrug resistance; Cancer therapy; Inhibitors; ABC transporters; ACUTE MYELOID-LEUKEMIA; BREAST-CANCER CELLS; P-GLYCOPROTEIN INHIBITORS; TYROSINE KINASE INHIBITOR; WNT/BETA-CATENIN PATHWAY; DOWN-REGULATION; GASTRIC-CANCER; PROTEIN BCRP/ABCG2; IN-VIVO; MDR1/P-GLYCOPROTEIN EXPRESSION;
D O I
10.1016/j.canlet.2015.10.010
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Multidrug resistance (MDR) is a serious phenomenon employed by cancer cells which hampers the success of cancer pharmacotherapy. One of the common mechanisms of MDR is the overexpression of ATP-binding cassette (ABC) efflux transporters in cancer cells such as P-glycoprotein (P-gp/ABCB1), multidrug resistance-associated protein 2 (MRP2/ABCC2), and breast cancer resistance protein (BCRP/ABCG2) that limits the prolonged and effective use of chemotherapeutic drugs. Researchers have found that developing inhibitors of ABC efflux transporters as chemosensitizers could overcome MDR. But the clinical trials have shown that most of these chemosensitizers are merely toxic and only show limited or no benefits to cancer patients, thus new inhibitors are being explored. Recent findings also suggest that efflux pumps of the ABC transporter family are subject to epigenetic gene regulation. In this review, we summarize recent findings of the role of ABC efflux transporters in MDR. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:153 / 164
页数:12
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