Nanotherapeutics approaches to overcome P-glycoprotein-mediated multi-drug resistance in cancer

被引:66
|
作者
Halder, Jitu [1 ]
Pradhan, Deepak [1 ]
Kar, Biswakanth [1 ]
Ghosh, Goutam [1 ]
Rath, Goutam [1 ]
机构
[1] Siksha O Anusandhan Deemed Univ, Sch Pharmaceut Sci, Bhubaneswar, Odisha, India
关键词
P-glycoprotein; Nanomaterials; P-gp inhibition; Acquired P-gp overexpression; Nanomedicine; Cancer; DRUG-RESISTANCE; INHIBITION; NANOPARTICLES; DOXORUBICIN; ABSORPTION; PACLITAXEL; DELIVERY; INSIGHT; IMPACT; CELLS;
D O I
10.1016/j.nano.2021.102494
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Multidrug resistance (MDR) in cancer chemotherapy is a growing concern for medical practitioners. P-glycoprotein (P-gp) overexpression is one of the major reasons for multidrug resistance in cancer chemotherapy. The P-gp overexpression in cancer cells depends on several factors like adenosine triphosphate (ATP) hydrolysis, hypoxia-inducible factor 1 alpha (HIF-1 alpha), and drug physicochemical properties such as lipophilicity, molecular weight, and molecular size. Further multiple exposures of anticancer drugs to the P-gp efflux protein cause acquired P-gp overexpression. Unique structural and functional characteristics of nanotechnology-based drug delivery systems provide opportunities to circumvent P-gp mediated MDR. The primary mechanism behind the nanocarrier systems in P-gp inhibition includes: bypassing or inhibiting the P-gp efflux pump to combat MDR. In this review, we discuss the role of P-gp in MDR and highlight the recent progress in different nanocarriers to overcome P-gp mediated MDR in terms of their limitations and potentials. (C) 2021 Elsevier Inc. All rights reserved.
引用
收藏
页数:17
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