细胞毒性T细胞
癌症治疗
癌症研究
癌症
肿瘤细胞
癌细胞
细胞毒性
化学
生物
医学
内科学
生物化学
体外
作者
Weijia Xu,Mingda Yang,J. Wang,Jie Li,Menghua Xiong,Ziyang Cao,Xianzhu Yang
出处
期刊:Nano Letters
[American Chemical Society]
日期:2025-06-10
标识
DOI:10.1021/acs.nanolett.5c02019
摘要
The highly selective ability of cytotoxic T lymphocytes (CTLs) to eliminate tumor cells has inspired the development of artificial nanomedicine for effective cancer therapy. Here, an artificial CTL (aCTL) that selectively recognizes and kills cancer cells is developed. The membrane target-binding moiety, membrane-perforating peptides, and therapeutic prodrugs are integrated into the aCTL through supramolecular interactions. Consequently, the prepared aCTL selectively binds cancer cells and perforates the surrounding membrane. Subsequently, the conjugated prodrug is cleaved and released by the overexpressed membrane transpeptidase, allowing entry into tumor cells through the perforated holes. Finally, the aCTL significantly suppresses the growth of HepG2 hepatocellular carcinoma, B16-F10 melanomas, and patient-derived xenograft (PDX) breast cancer models.
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