跨细胞
内体
卵巢癌
药物输送
化学
医学
细胞生物学
内科学
生物
癌症
生物化学
细胞内
内吞作用
受体
有机化学
作者
Lei Feng,Yao Pan,Jin-Heng Li,Suinan Sha,Xiubo Shi,Haoyan Guo,Chengzhi Huang,Qian Xiao,Fan Chen,Xingmei Zhang,Jun-Bing Fan,Ying Wang
标识
DOI:10.1016/j.apsb.2023.04.006
摘要
Extracellular vesicles (EVs) have recently received much attention about the application of drug carriers due to their desirable properties such as nano-size, biocompatibility, and high stability. Herein, we demonstrate orange-derived extracellular vesicles (OEV) nanodrugs ([email protected]) by modifying cRGD-targeted doxorubicin (DOX) nanoparticles (DN) onto the surface of OEV, enabling significantly enhancing tumor accumulation and penetration, thereby efficiently inhibiting the growth of ovarian cancer. The obtained [email protected] enabled to inducement of greater transcytosis capability in ovarian cancer cells, which presented the average above 10-fold transcytosis effect compared with individual DN. It was found that [email protected] could trigger receptor-mediated endocytosis to promote early endosome/recycling endosomes pathway for exocytosis and simultaneously reduce degradation in the early endosomes-late endosomes-lysosome pathway, thereby inducing the enhanced transcytosis. In particular, the zombie mouse model bearing orthotopic ovarian cancer further validated [email protected] presented high accumulation and penetration in tumor tissue by the transcytosis process. Our study indicated the strategy in enhancing transcytosis has significant implications for improving the therapeutic efficacy of the drug delivery system.
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