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Engineering blood exosomes for tumor-targeting efficient gene/chemo combination therapy

Rationale: Developing an effective nanoplatform to realize 'multi-in-one' is essential to broaden the therapeutic potential of combination therapy. Exosomes are ideal candidates since their intrinsic abilities of integrating multiple contents and functions. However, only limited efforts ha...

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Autores principales: Zhan, Qi, Yi, Kaikai, Qi, Hongzhao, Li, Sidi, Li, Xueping, Wang, Qixue, Wang, Yunfei, Liu, Chaoyong, Qiu, Mingzhe, Yuan, Xubo, Zhao, Jin, Hou, Xin, Kang, Chunsheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7359100/
https://www.ncbi.nlm.nih.gov/pubmed/32685027
http://dx.doi.org/10.7150/thno.45028
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author Zhan, Qi
Yi, Kaikai
Qi, Hongzhao
Li, Sidi
Li, Xueping
Wang, Qixue
Wang, Yunfei
Liu, Chaoyong
Qiu, Mingzhe
Yuan, Xubo
Zhao, Jin
Hou, Xin
Kang, Chunsheng
author_facet Zhan, Qi
Yi, Kaikai
Qi, Hongzhao
Li, Sidi
Li, Xueping
Wang, Qixue
Wang, Yunfei
Liu, Chaoyong
Qiu, Mingzhe
Yuan, Xubo
Zhao, Jin
Hou, Xin
Kang, Chunsheng
author_sort Zhan, Qi
collection PubMed
description Rationale: Developing an effective nanoplatform to realize 'multi-in-one' is essential to broaden the therapeutic potential of combination therapy. Exosomes are ideal candidates since their intrinsic abilities of integrating multiple contents and functions. However, only limited efforts have been devoted to engineering exosomes to integrate the needed properties, also considering the safety and yield, for tumor-targeted and efficient gene/chemo combination therapy. Methods: Herein, by manipulating the exosome membrane, blood exosomes with high abundance and safety are engineered as a versatile combinatorial delivery system, where the doxorubicin (Dox) and cholesterol-modified miRNA21 inhibitor (miR-21i) are co-embedded into the lipid bilayer of exosomes, and the magnetic molecules and endosomolytic peptides L17E are bind to the exosome membrane through ligand-receptor coupling and electrostatic interactions, respectively. Results: It is proved that such engineering strategy not only preserves their intrinsic features, but also readily integrates multiple properties of tumor targeting, efficient transfection and gene/chemo combination therapy into blood exosomes. The lipid bilayer structure of exosomes allows them to co-load Dox and miR-21i with high-payloads. Moreover, profiting from the integration of magnetic molecules and L17E peptides, the engineered exosomes exhibit an enhanced tumor accumulation and an improved endosome escape ability, thereby specifically and efficiently delivering encapsulated cargos to tumor cells. As a result, a remarkable inhibition of tumor growth is observed in the tumor-bearing mice, and without noticeable side effects. Conclusions: This study demonstrates the potential of engineered blood exosomes as feasible co-delivery nanosystem for tumor-targeted and efficient combination therapy. Further development by replacing the drugs combined regimens can potentially make this engineered exosome become a general platform for the design of safe and effective combination therapy modality.
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spelling pubmed-73591002020-07-17 Engineering blood exosomes for tumor-targeting efficient gene/chemo combination therapy Zhan, Qi Yi, Kaikai Qi, Hongzhao Li, Sidi Li, Xueping Wang, Qixue Wang, Yunfei Liu, Chaoyong Qiu, Mingzhe Yuan, Xubo Zhao, Jin Hou, Xin Kang, Chunsheng Theranostics Research Paper Rationale: Developing an effective nanoplatform to realize 'multi-in-one' is essential to broaden the therapeutic potential of combination therapy. Exosomes are ideal candidates since their intrinsic abilities of integrating multiple contents and functions. However, only limited efforts have been devoted to engineering exosomes to integrate the needed properties, also considering the safety and yield, for tumor-targeted and efficient gene/chemo combination therapy. Methods: Herein, by manipulating the exosome membrane, blood exosomes with high abundance and safety are engineered as a versatile combinatorial delivery system, where the doxorubicin (Dox) and cholesterol-modified miRNA21 inhibitor (miR-21i) are co-embedded into the lipid bilayer of exosomes, and the magnetic molecules and endosomolytic peptides L17E are bind to the exosome membrane through ligand-receptor coupling and electrostatic interactions, respectively. Results: It is proved that such engineering strategy not only preserves their intrinsic features, but also readily integrates multiple properties of tumor targeting, efficient transfection and gene/chemo combination therapy into blood exosomes. The lipid bilayer structure of exosomes allows them to co-load Dox and miR-21i with high-payloads. Moreover, profiting from the integration of magnetic molecules and L17E peptides, the engineered exosomes exhibit an enhanced tumor accumulation and an improved endosome escape ability, thereby specifically and efficiently delivering encapsulated cargos to tumor cells. As a result, a remarkable inhibition of tumor growth is observed in the tumor-bearing mice, and without noticeable side effects. Conclusions: This study demonstrates the potential of engineered blood exosomes as feasible co-delivery nanosystem for tumor-targeted and efficient combination therapy. Further development by replacing the drugs combined regimens can potentially make this engineered exosome become a general platform for the design of safe and effective combination therapy modality. Ivyspring International Publisher 2020-06-22 /pmc/articles/PMC7359100/ /pubmed/32685027 http://dx.doi.org/10.7150/thno.45028 Text en © The author(s) This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Zhan, Qi
Yi, Kaikai
Qi, Hongzhao
Li, Sidi
Li, Xueping
Wang, Qixue
Wang, Yunfei
Liu, Chaoyong
Qiu, Mingzhe
Yuan, Xubo
Zhao, Jin
Hou, Xin
Kang, Chunsheng
Engineering blood exosomes for tumor-targeting efficient gene/chemo combination therapy
title Engineering blood exosomes for tumor-targeting efficient gene/chemo combination therapy
title_full Engineering blood exosomes for tumor-targeting efficient gene/chemo combination therapy
title_fullStr Engineering blood exosomes for tumor-targeting efficient gene/chemo combination therapy
title_full_unstemmed Engineering blood exosomes for tumor-targeting efficient gene/chemo combination therapy
title_short Engineering blood exosomes for tumor-targeting efficient gene/chemo combination therapy
title_sort engineering blood exosomes for tumor-targeting efficient gene/chemo combination therapy
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7359100/
https://www.ncbi.nlm.nih.gov/pubmed/32685027
http://dx.doi.org/10.7150/thno.45028
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