A self-delivery membrane system for enhanced anti-tumor therapy

被引:45
|
作者
Qiu, Wen-Xiu
Zhang, Ming-Kang
Liu, Li-Han
Gao, Fan
Zhang, Lu
Li, Shi-Ying
Xie, Bo-Ru
Zhang, Chi
Feng, Jun
Zhang, Xian-Zheng [1 ]
机构
[1] Wuhan Univ, Minist Educ, Key Lab Biomed Polymers, Wuhan 430072, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
Chimeric peptide; Self-delivery; Membrane target; Anti-tumor therapy; Immune response; DRUG-DELIVERY; CELL-MEMBRANE; PHOTODYNAMIC THERAPY; COATED NANOPARTICLES; CIRCULATION TIME; BREAST-CANCER; MICELLES; PH; INTERNALIZATION; TOXICITY;
D O I
10.1016/j.biomaterials.2018.01.037
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Nowadays, cell membrane targeting therapy has drawn much attention for its high anti-tumor effect by avoiding the cellular barriers. In this study, therapeutic agent conjugated chimeric peptide (Cp) was anchored in cracked cancer cell membranes (CCCM) to construct a self-delivery membrane system (MCp), which could relize precise cell membrane targeting therapy. It was found that compared with Cp, MCp could target to the cancer cell membrane with longer retention time, which is very crucial for in vivo applications. And the superior cell membrane targeting ability was attributed to the specific proteins (focal adhesion proteins, focal adhesion kinase, RHO family proteins, and integrin) on the CCCM surface. Importantly, the M-Cp could promote tumor-specific immune response, which further enhanced antitumor effect when combined with therapeutic agents in M-Cp. What's more, this self-delivery membrane system could be used as a template for cell membrane targeting therapy by changing the therapeutic agents as well as the CCCM, and this strategy would open a new window for various cell membrane targeting therapy. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:81 / 94
页数:14
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