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

[Image: see text] Extracellular vesicles (EVs), or exosomes, play a pivotal role in tumor growth and metastasis, such as in the case of Kaposi Sarcoma. By loading tumor-derived EVs with chemotherapeutic drugs, we noted that their pro-tumor/pro-angiogenic phenotype was converted into an anti-tumor ph...

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Autores principales: McNamara, Ryan P., Eason, Anthony B., Zhou, Yijun, Bigi, Rachele, Griffith, Jack D., Costantini, Lindsey M., Rudek, Michelle A., Anders, Nicole M., Damania, Blossom A., Dittmer, Dirk P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9026271/
https://www.ncbi.nlm.nih.gov/pubmed/35480227
http://dx.doi.org/10.1021/acsbiomedchemau.1c00030
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author McNamara, Ryan P.
Eason, Anthony B.
Zhou, Yijun
Bigi, Rachele
Griffith, Jack D.
Costantini, Lindsey M.
Rudek, Michelle A.
Anders, Nicole M.
Damania, Blossom A.
Dittmer, Dirk P.
author_facet McNamara, Ryan P.
Eason, Anthony B.
Zhou, Yijun
Bigi, Rachele
Griffith, Jack D.
Costantini, Lindsey M.
Rudek, Michelle A.
Anders, Nicole M.
Damania, Blossom A.
Dittmer, Dirk P.
author_sort McNamara, Ryan P.
collection PubMed
description [Image: see text] Extracellular vesicles (EVs), or exosomes, play a pivotal role in tumor growth and metastasis, such as in the case of Kaposi Sarcoma. By loading tumor-derived EVs with chemotherapeutic drugs, we noted that their pro-tumor/pro-angiogenic phenotype was converted into an anti-tumor phenotype in vivo. Drug concentration in EVs was significantly higher than in clinically approved liposome formulation, as retention was facilitated by the presence of miRNAs inside the natural EVs. This demonstrates a new mechanism by which to increase the payload capacity of nanoparticles. By exploiting the targeting preferences of tumor-derived EVs, chemotherapeutics can be directed to specifically poison the cells and the microenvironment that enables metastasis.
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spelling pubmed-90262712022-04-25 Exosome-Encased Nucleic Acid Scaffold Chemotherapeutic Agents for Superior Anti-Tumor and Anti-Angiogenesis Activity McNamara, Ryan P. Eason, Anthony B. Zhou, Yijun Bigi, Rachele Griffith, Jack D. Costantini, Lindsey M. Rudek, Michelle A. Anders, Nicole M. Damania, Blossom A. Dittmer, Dirk P. ACS Bio Med Chem Au [Image: see text] Extracellular vesicles (EVs), or exosomes, play a pivotal role in tumor growth and metastasis, such as in the case of Kaposi Sarcoma. By loading tumor-derived EVs with chemotherapeutic drugs, we noted that their pro-tumor/pro-angiogenic phenotype was converted into an anti-tumor phenotype in vivo. Drug concentration in EVs was significantly higher than in clinically approved liposome formulation, as retention was facilitated by the presence of miRNAs inside the natural EVs. This demonstrates a new mechanism by which to increase the payload capacity of nanoparticles. By exploiting the targeting preferences of tumor-derived EVs, chemotherapeutics can be directed to specifically poison the cells and the microenvironment that enables metastasis. American Chemical Society 2022-01-20 /pmc/articles/PMC9026271/ /pubmed/35480227 http://dx.doi.org/10.1021/acsbiomedchemau.1c00030 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle McNamara, Ryan P.
Eason, Anthony B.
Zhou, Yijun
Bigi, Rachele
Griffith, Jack D.
Costantini, Lindsey M.
Rudek, Michelle A.
Anders, Nicole M.
Damania, Blossom A.
Dittmer, Dirk P.
Exosome-Encased Nucleic Acid Scaffold Chemotherapeutic Agents for Superior Anti-Tumor and Anti-Angiogenesis Activity
title Exosome-Encased Nucleic Acid Scaffold Chemotherapeutic Agents for Superior Anti-Tumor and Anti-Angiogenesis Activity
title_full Exosome-Encased Nucleic Acid Scaffold Chemotherapeutic Agents for Superior Anti-Tumor and Anti-Angiogenesis Activity
title_fullStr Exosome-Encased Nucleic Acid Scaffold Chemotherapeutic Agents for Superior Anti-Tumor and Anti-Angiogenesis Activity
title_full_unstemmed Exosome-Encased Nucleic Acid Scaffold Chemotherapeutic Agents for Superior Anti-Tumor and Anti-Angiogenesis Activity
title_short Exosome-Encased Nucleic Acid Scaffold Chemotherapeutic Agents for Superior Anti-Tumor and Anti-Angiogenesis Activity
title_sort exosome-encased nucleic acid scaffold chemotherapeutic agents for superior anti-tumor and anti-angiogenesis activity
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9026271/
https://www.ncbi.nlm.nih.gov/pubmed/35480227
http://dx.doi.org/10.1021/acsbiomedchemau.1c00030
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