The therapeutic potential of targeting ABC transporters to combat multi-drug resistance

被引:114
作者
Bugde, Piyush [1 ]
Biswas, Riya [1 ]
Merien, Fabrice [1 ,2 ]
Lu, Jun [1 ,3 ]
Liu, Dong-Xu [1 ]
Chen, Mingwei [4 ]
Zhou, Shufeng [5 ]
Li, Yan [1 ,3 ]
机构
[1] Auckland Univ Technol, Sch Sci, Auckland, New Zealand
[2] Auckland Univ Technol, AUT Roche Diagnost Lab, Sch Sci, Auckland, New Zealand
[3] Auckland Univ Technol, Sch Interprofess Hlth Studies, Auckland, New Zealand
[4] Xi An Jiao Tong Univ, Affiliated Hosp 1, Dept Resp Med, Xian, Peoples R China
[5] Huaqiao Univ, Coll Chem Engn, Dept Biotechnol & Bioengn, Xiamen, Peoples R China
关键词
ABC transporter; pharmacokinetics; multidrug resistance; cancer; nanotechnology; ORGANIC ANION TRANSPORTER; CELL LUNG-CANCER; P-GLYCOPROTEIN INHIBITOR; CONJUGATE EXPORT PUMP; BINDING CASSETTE TRANSPORTERS; SINGLE NUCLEOTIDE POLYMORPHISMS; DRUG EFFLUX TRANSPORTERS; CHRONIC MYELOID-LEUKEMIA; KIDNEY PROXIMAL TUBULES; CULTURED MURINE CELLS;
D O I
10.1080/14728222.2017.1310841
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Most disseminated cancers remain fatal despite the availability of a variety of conventional and novel treatments including surgery, chemotherapy, radiotherapy, immunotherapy, and biologically targeted therapy. A major factor responsible for the failure of chemotherapy in the treatment of cancer is the development of multidrug resistance (MDR). The overexpression of various ABC transporters in cancer cells can efficiently remove the anticancer drug from the cell, thus causing the drug to lose its effect.Areas covered: In this review, we summarised the ongoing research related to the mechanism, function, and regulation of ABC transporters. We integrated our current knowledge at different levels from molecular biology to clinical trials. We also discussed potential therapeutic strategies of targeting ABC transporters to reverse MDR in cancer cells.Expert opinion: Involvement of various ABC transporters to cancer MDR lays the foundation for developing tailored therapies that can overcome MDR. An ideal MDR reversal agent should have broad-spectrum ABC-transporter inhibitory activity, be potent, have good pharmacokinetics, have no trans-stimulation effects, and have low or no toxicity. Alternatively, nanotechnology-based drug delivery systems containing both the cytotoxic drug and reversing agent may represent a useful approach to reversing MDR with minimal off-target toxicity.
引用
收藏
页码:511 / 530
页数:20
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