A targeted nanoplatform co-delivery of pooled siRNA and doxorubicin for reversing of multidrug resistance in breast cancer

被引:16
|
作者
Liu, Hongmei [1 ,2 ]
Ma, Ding [3 ]
Chen, Jinpeng [4 ]
Ye, Li [2 ]
Li, Yiping [5 ]
Xie, Yuexia [2 ]
Zhao, Xue [2 ]
Zou, Hanbing [2 ]
Chen, Xiaojing [2 ]
Pu, Jun [1 ]
Liu, Peifeng [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Renji Hosp, Shanghai Canc Inst, State Key Lab Oncogenes & Related Genes,Sch Med, Shanghai 200032, Peoples R China
[2] Shanghai Jiao Tong Univ, Renji Hosp, Sch Med, Cent Lab, Shanghai 200127, Peoples R China
[3] Shanghai Jiao Tong Univ, Dept Biliary Pancreat Surg, Sch Med, Renji Hosp, Shanghai 200127, Peoples R China
[4] Nantong First Peoples Hosp, Thyroid Breast Surg, Nantong 226001, Peoples R China
[5] Shanghai Univ Tradit Chinese Med, Shanghai 200032, Peoples R China
基金
上海市自然科学基金; 中国国家自然科学基金;
关键词
multi-drug resistance (MDR); breast cancer; adenosine triphosphate (ATP) responsiveness; epsilon-polylysine; POLY-L-LYSINE; DENDRIMERS; CELL; NANOPARTICLES; GLYCOPROTEIN; CHEMOTHERAPY; EFFICACY; FAMILY;
D O I
10.1007/s12274-022-4254-1
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Multi-drug resistance (MDR) has become the largest obstacle to the success of cancer patients receiving traditional chemotherapeutics or novel targeted drugs. Here, we developed a targeted nanoplatform based on biodegradable boronic acid modified epsilon-polylysine to co-deliver P-gp siRNA, Bcl-2 siRNA, and doxorubicin for overcoming the challenge. The targeted nanoplatform showed a robust suppressing efficiency for the invasion, proliferation, and colony formation of adriamycin (ADR) resistant breast cancer cell line (MCF-7/ADR) cells in vitro. The ATP responsiveness of the nanoplatform was also proved in the research. In the in vivo antitumor experiment, the targeted nanoplatform showed a significant inhibition of tumor growth with good biocompatibility. The goal of this study is to develop a novel and facile strategy to prepare a highly efficient and safe gene and drug delivery system for MDR breast cancer based on biocompatible epsilon-polylysine polymers.
引用
收藏
页码:6306 / 6314
页数:9
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