Exosome-Encased Nucleic Acid Scaffold Chemotherapeutic Agents for Superior Anti-Tumor and Anti-Angiogenesis Activity

被引:5
|
作者
McNamara, Ryan P. [1 ,2 ]
Eason, Anthony B. [1 ,2 ]
Zhou, Yijun [1 ,2 ]
Bigi, Rachele [1 ,2 ]
Griffith, Jack D. [1 ,2 ]
Costantini, Lindsey M. [1 ,2 ,3 ]
Rudek, Michelle A. [4 ]
Anders, Nicole M. [4 ]
Damania, Blossom A. [1 ,2 ]
Dittmer, Dirk P. [1 ,2 ]
机构
[1] Univ N Carolina, Sch Med, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Sch Med, Dept Microbiol & Immunol, Chapel Hill, NC 27599 USA
[3] North Carolina Cent Univ, Dept Biol & Biomed Sci, Durham, NC 27707 USA
[4] Johns Hopkins Sch Med, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD 21205 USA
来源
ACS BIO & MED CHEM AU | 2022年 / 2卷 / 02期
关键词
exosome; extracellular vesicles; drug delivery; Kaposi's sarcoma; virology; PEGYLATED-LIPOSOMAL DOXORUBICIN; EXTRACELLULAR VESICLES; COMMUNICATION; FLUORESCENCE; PACLITAXEL; DELIVERY; SARCOMA;
D O I
10.1021/acsbiomedchemau.1c00030
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Extracellular vesicles(EVs), or exosomes, play a pivotal rolein tumor growth and metastasis, such as in the case of Kaposi Sarcoma.By loading tumor-derived EVs with chemotherapeutic drugs, we notedthat their pro-tumor/pro-angiogenic phenotype was converted into ananti-tumor phenotype in vivo. Drug concentrationin EVs was significantly higher than in clinically approved liposomeformulation, as retention was facilitated by the presence of miRNAsinside the natural EVs. This demonstrates a new mechanism by whichto increase the payload capacity of nanoparticles. By exploiting thetargeting preferences of tumor-derived EVs, chemotherapeutics canbe directed to specifically poison the cells and the microenvironmentthat enables metastasis.
引用
收藏
页码:140 / 149
页数:10
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