Different strategies to overcome multidrug resistance in cancer

被引:225
|
作者
Saraswathy, Manju
Gong, Shaoqin [1 ]
机构
[1] Univ Wisconsin, Dept Biomed Engn, Madison, WI 53715 USA
基金
美国国家科学基金会;
关键词
Cancer; Multidrug resistance; Chemosensitizers; Anticancer agents; Nanocarriers; RNAi therapy; SMALL INTERFERING RNA; NF-KAPPA-B; SHORT-HAIRPIN RNA; P-GLYCOPROTEIN; DRUG-RESISTANCE; CO-DELIVERY; BREAST-CANCER; CHEMOTHERAPY RESISTANCE; INDUCED SUPPRESSION; DNA TOPOISOMERASE;
D O I
10.1016/j.biotechadv.2013.06.004
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The risk of acquisition of resistance to chemotherapy remains a major hurdle in the management of various types of cancer patients. Several cellular and noncellular mechanisms are involved in developing both intrinsic and acquired resistance in cancer cells toward chemotherapy. This review covers the various multidrug resistance (MDR) mechanisms observed in cancer cells as well as the various strategies developed to overcome these MDR mechanisms. Extensive studies have been conducted during the last several decades to enhance the efficacy of chemotherapy by suppressing or evading these MDR mechanisms including the use of new anticancer drugs that could escape from the efflux reaction, MDR modulators or chemosensitizers, multifunctional nanocarriers, and RNA interference (RNAi) therapy. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:1397 / 1407
页数:11
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