The reversal of chemotherapy-induced multidrug resistance by nanomedicine for cancer therapy

被引:88
作者
Liu, Shangui [1 ]
Khan, Abdur Rauf [1 ]
Yang, Xiaoye [1 ]
Dong, Bo [2 ]
Ji, Jianbo [1 ]
Zhai, Guangxi [1 ]
机构
[1] Shandong Univ, Sch Pharmaceut Sci, Dept Pharmaceut, Key Lab Chem Biol,Minist Educ, Jinan 250012, Peoples R China
[2] Shandong Prov Hosp, Dept Cardiovasc Med, Jinan 250021, Peoples R China
关键词
Multidrug resistance; Nanoparticles; P-glycoprotein (P-gp); Subcellular organelle targeting; Combination therapy; CSCs therapy; OVERCOMING DRUG-RESISTANCE; VITAMIN-E-TPGS; MULTIFUNCTIONAL POLYMERIC MICELLES; MESOPOROUS SILICA NANOPARTICLES; ANTI-ABCG2; MONOCLONAL-ANTIBODY; ULTRASMALL GOLD NANOPARTICLES; TARGETED INTRACELLULAR DRUG; ALBUMIN-BOUND PACLITAXEL; CO-DELIVERY; BREAST-CANCER;
D O I
10.1016/j.jconrel.2021.05.012
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Multidrug resistance (MDR) of cancer is a persistent problem in chemotherapy. Scientists have considered the overexpressed efflux transporters responsible for MDR and chemotherapy failure. MDR extremely limits the therapeutic effect of chemotherapy in cancer treatment. Many strategies have been applied to solve this problem. Multifunctional nanoparticles may be one of the most promising approaches to reverse MDR of tumor. These nanoparticles can keep stability in the blood circulation and selectively accumulated in the tumor microenvironment (TME) either by passive or active targeting. The stimuli-sensitive or organelle-targeting nanoparticles can release the drug at the targeted-site without exposure to normal tissues. In order to better understand reversal of MDR, three main strategies are concluded in this review. First strategy is the synergistic effect of chemotherapeutic drugs and ABC transporter inhibitors. Through directly inhibiting overexpressed ABC transporters, chemotherapeutic drugs can enter into resistant cells without being efflux. Second strategy is based on nanoparticles circumventing over-expressed efflux transporters and directly targeting resistance-related organelles. Third approach is the combination of multiple therapy modes overcoming cancer resistance. At last, numerous researches demonstrated cancer stem-like cells (CSCs) had a deep relation with drug resistance. Here, we discuss two different drug delivery approaches of nanomedicine based on CSC therapy.
引用
收藏
页码:1 / 20
页数:20
相关论文
共 340 条
[1]   The recent progresses in shRNA-nanoparticle conjugate as a therapeutic approach [J].
Acharya, Rituparna .
MATERIALS SCIENCE AND ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS, 2019, 104
[2]  
Alavi Mehran, 2019, Drug Metabolism and Personalized Therapy, V34, P20180032, DOI 10.1515/dmpt-2018-0032
[3]   What sustains the multidrug resistance phenotype beyond ABC efflux transporters? Looking beyond the tip of the iceberg [J].
Alexa-Stratulat, Teodora ;
Pesic, Milica ;
Gasparovic, Ana Cipak ;
Trougakos, Ioannis P. ;
Riganti, Chiara .
DRUG RESISTANCE UPDATES, 2019, 46
[4]   Ligand density on nanoparticles: A parameter with critical impact on nanomedicine [J].
Alkilany, Alaaldin M. ;
Zhu, Lin ;
Weller, Horst ;
Mews, Alf ;
Parak, Wolfgang J. ;
Barz, Matthias ;
Feliu, Neus .
ADVANCED DRUG DELIVERY REVIEWS, 2019, 143 :22-36
[5]   P-glycoprotein: from genomics to mechanism [J].
Ambudkar, SV ;
Kimchi-Sarfaty, C ;
Sauna, ZE ;
Gottesman, MM .
ONCOGENE, 2003, 22 (47) :7468-7485
[6]   ROS-augmented and tumor-microenvironment responsive biodegradable nanoplatform for enhancing chemo-sonodynamic therapy [J].
An, Jie ;
Hu, Yong-Guo ;
Cheng, Kai ;
Li, Cheng ;
Hou, Xiao-Lin ;
Wang, Gang-Lin ;
Zhang, Xiao-Shuai ;
Liu, Bo ;
Zhao, Yuan-Di ;
Zhang, Ming-Zhen .
BIOMATERIALS, 2020, 234
[7]   The glucocorticoid receptor: Pivot of depression and of antidepressant treatment? [J].
Anacker, Christoph ;
Zunszain, Patricia A. ;
Carvalho, Livia A. ;
Pariante, Carmine M. .
PSYCHONEUROENDOCRINOLOGY, 2011, 36 (03) :415-425
[8]   Novel targets and interaction partners of mutant p53 Gain-Of-Function [J].
Aschauer, Lydia ;
Muller, Patricia A. J. .
BIOCHEMICAL SOCIETY TRANSACTIONS, 2016, 44 :460-466
[9]   Improving Cancer Chemoradiotherapy Treatment by Dual Controlled Release of Wortmannin and Docetaxel in Polymeric Nanoparticles [J].
Au, Kin Man ;
Min, Yuanzeng ;
Tian, Xi ;
Zhang, Longzhen ;
Perello, Virginia ;
Caster, Joseph M. ;
Wang, Andrew Z. .
ACS NANO, 2015, 9 (09) :8976-8996
[10]   Controlled release and reversal of multidrug resistance by co-encapsulation of paclitaxel and verapamil in solid lipid nanoparticles [J].
Baek, Jong-Suep ;
Cho, Cheong-Weon .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2015, 478 (02) :617-624