| Literature DB >> 29217761 |
Yuan Wan1,2, Lixue Wang3,4, Chuandong Zhu3, Qin Zheng3, Guoxiang Wang5, Jinlong Tong3, Yuan Fang3, Yiqiu Xia6,2, Gong Cheng6,2, Xia He7, Si-Yang Zheng1,2,8,9.
Abstract
Extracellular nanovesicles (ENV) released by many cells contain lipids, proteins, and nucleic acids that contribute to intercellular communication. ENVs have emerged as biomarkers and therapeutic targets but they have also been explored as drug delivery vehicles. However, for the latter application, clinical translation has been limited by low yield and inadequate targeting effects. ENV vectors with desired targeting properties can be produced from parental cells engineered to express membrane-bound targeting ligands, or they can be generated by fusion with targeting liposomes; however, neither approach has met clinical requirements. In this study, we demonstrate that mechanical extrusion of approximately 107 cells grafted with lipidated ligands can generate cancer cell-targeting ENV and can be prepared in approximately 1 hour. This rapid and economic approach could pave the way for clinical implementation in the future.Significance: A new and rapid method for production of drug-targeting nanovesicles has implications for cancer treatment by chimeric antigen receptor T cells and other therapies. Cancer Res; 78(3); 798-808. ©2017 AACR. ©2017 American Association for Cancer Research.Entities:
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Year: 2017 PMID: 29217761 PMCID: PMC5811376 DOI: 10.1158/0008-5472.CAN-17-2880
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701