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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.
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页数:17
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