Cargando…
Exosome mimetics derived from bone marrow mesenchymal stem cells deliver doxorubicin to osteosarcoma in vitro and in vivo
Osteosarcoma is a bone tumor with a high incidence in children and adolescents. Chemotherapy for osteosarcoma is limited, and effective targeted drugs are urgently needed to treat osteosarcoma. Exosomes as a natural nano drug delivery platform have been widely studied and proven to have good drug de...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9662035/ https://www.ncbi.nlm.nih.gov/pubmed/36352741 http://dx.doi.org/10.1080/10717544.2022.2141921 |
_version_ | 1784830605793427456 |
---|---|
author | Wang, Jinkui Li, Mujie Jin, Liming Guo, Peng Zhang, Zhaoxia Zhanghuang, Chenghao Tan, Xiaojun Mi, Tao Liu, Jiayan Wu, Xin Wei, Guanghui He, Dawei |
author_facet | Wang, Jinkui Li, Mujie Jin, Liming Guo, Peng Zhang, Zhaoxia Zhanghuang, Chenghao Tan, Xiaojun Mi, Tao Liu, Jiayan Wu, Xin Wei, Guanghui He, Dawei |
author_sort | Wang, Jinkui |
collection | PubMed |
description | Osteosarcoma is a bone tumor with a high incidence in children and adolescents. Chemotherapy for osteosarcoma is limited, and effective targeted drugs are urgently needed to treat osteosarcoma. Exosomes as a natural nano drug delivery platform have been widely studied and proven to have good drug delivery performance. However, the low production of exosomes hinders its development as a carrier. Exosome mimetics (EMs) as an alternative product of exosomes solve the problem of low production of exosomes and maintain the good performance of exosomes as carriers. In this study, bone marrow mesenchymal stem cells (BMSCs) were sequentially extruded to generate EMs to encapsulate doxorubicin (EM-Dox) to treat osteosarcoma. The results showed that we successfully prepared EMs of BMSC, and EM-Dox was prepared using an active-loading approach. Our engineered EM-Dox demonstrated significantly more potent tumor inhibition activity and fewer side effects than free doxorubicin. This novel biological nanomedicine system provides a promising opportunity to develop novel precision medicine for osteosarcoma. |
format | Online Article Text |
id | pubmed-9662035 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-96620352022-11-15 Exosome mimetics derived from bone marrow mesenchymal stem cells deliver doxorubicin to osteosarcoma in vitro and in vivo Wang, Jinkui Li, Mujie Jin, Liming Guo, Peng Zhang, Zhaoxia Zhanghuang, Chenghao Tan, Xiaojun Mi, Tao Liu, Jiayan Wu, Xin Wei, Guanghui He, Dawei Drug Deliv Research Articles Osteosarcoma is a bone tumor with a high incidence in children and adolescents. Chemotherapy for osteosarcoma is limited, and effective targeted drugs are urgently needed to treat osteosarcoma. Exosomes as a natural nano drug delivery platform have been widely studied and proven to have good drug delivery performance. However, the low production of exosomes hinders its development as a carrier. Exosome mimetics (EMs) as an alternative product of exosomes solve the problem of low production of exosomes and maintain the good performance of exosomes as carriers. In this study, bone marrow mesenchymal stem cells (BMSCs) were sequentially extruded to generate EMs to encapsulate doxorubicin (EM-Dox) to treat osteosarcoma. The results showed that we successfully prepared EMs of BMSC, and EM-Dox was prepared using an active-loading approach. Our engineered EM-Dox demonstrated significantly more potent tumor inhibition activity and fewer side effects than free doxorubicin. This novel biological nanomedicine system provides a promising opportunity to develop novel precision medicine for osteosarcoma. Taylor & Francis 2022-11-09 /pmc/articles/PMC9662035/ /pubmed/36352741 http://dx.doi.org/10.1080/10717544.2022.2141921 Text en © 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Wang, Jinkui Li, Mujie Jin, Liming Guo, Peng Zhang, Zhaoxia Zhanghuang, Chenghao Tan, Xiaojun Mi, Tao Liu, Jiayan Wu, Xin Wei, Guanghui He, Dawei Exosome mimetics derived from bone marrow mesenchymal stem cells deliver doxorubicin to osteosarcoma in vitro and in vivo |
title | Exosome mimetics derived from bone marrow mesenchymal stem cells deliver doxorubicin to osteosarcoma in vitro and in vivo |
title_full | Exosome mimetics derived from bone marrow mesenchymal stem cells deliver doxorubicin to osteosarcoma in vitro and in vivo |
title_fullStr | Exosome mimetics derived from bone marrow mesenchymal stem cells deliver doxorubicin to osteosarcoma in vitro and in vivo |
title_full_unstemmed | Exosome mimetics derived from bone marrow mesenchymal stem cells deliver doxorubicin to osteosarcoma in vitro and in vivo |
title_short | Exosome mimetics derived from bone marrow mesenchymal stem cells deliver doxorubicin to osteosarcoma in vitro and in vivo |
title_sort | exosome mimetics derived from bone marrow mesenchymal stem cells deliver doxorubicin to osteosarcoma in vitro and in vivo |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9662035/ https://www.ncbi.nlm.nih.gov/pubmed/36352741 http://dx.doi.org/10.1080/10717544.2022.2141921 |
work_keys_str_mv | AT wangjinkui exosomemimeticsderivedfrombonemarrowmesenchymalstemcellsdeliverdoxorubicintoosteosarcomainvitroandinvivo AT limujie exosomemimeticsderivedfrombonemarrowmesenchymalstemcellsdeliverdoxorubicintoosteosarcomainvitroandinvivo AT jinliming exosomemimeticsderivedfrombonemarrowmesenchymalstemcellsdeliverdoxorubicintoosteosarcomainvitroandinvivo AT guopeng exosomemimeticsderivedfrombonemarrowmesenchymalstemcellsdeliverdoxorubicintoosteosarcomainvitroandinvivo AT zhangzhaoxia exosomemimeticsderivedfrombonemarrowmesenchymalstemcellsdeliverdoxorubicintoosteosarcomainvitroandinvivo AT zhanghuangchenghao exosomemimeticsderivedfrombonemarrowmesenchymalstemcellsdeliverdoxorubicintoosteosarcomainvitroandinvivo AT tanxiaojun exosomemimeticsderivedfrombonemarrowmesenchymalstemcellsdeliverdoxorubicintoosteosarcomainvitroandinvivo AT mitao exosomemimeticsderivedfrombonemarrowmesenchymalstemcellsdeliverdoxorubicintoosteosarcomainvitroandinvivo AT liujiayan exosomemimeticsderivedfrombonemarrowmesenchymalstemcellsdeliverdoxorubicintoosteosarcomainvitroandinvivo AT wuxin exosomemimeticsderivedfrombonemarrowmesenchymalstemcellsdeliverdoxorubicintoosteosarcomainvitroandinvivo AT weiguanghui exosomemimeticsderivedfrombonemarrowmesenchymalstemcellsdeliverdoxorubicintoosteosarcomainvitroandinvivo AT hedawei exosomemimeticsderivedfrombonemarrowmesenchymalstemcellsdeliverdoxorubicintoosteosarcomainvitroandinvivo |