| Literature DB >> 29421565 |
Wen-Xiu Qiu1, Ming-Kang Zhang1, Li-Han Liu1, Fan Gao1, Lu Zhang1, Shi-Ying Li1, Bo-Ru Xie1, Chi Zhang1, Jun Feng1, Xian-Zheng Zhang2.
Abstract
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 (M-Cp), which could relize precise cell membrane targeting therapy. It was found that compared with Cp, M-Cp 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 anti-tumor 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.Entities:
Keywords: Anti-tumor therapy; Chimeric peptide; Immune response; Membrane target; Self-delivery
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Year: 2018 PMID: 29421565 DOI: 10.1016/j.biomaterials.2018.01.037
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 12.479