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Engineered exosomes loaded with miR-449a selectively inhibit the growth of homologous non-small cell lung cancer
As an efficient drug carrier, exosome has been widely used in the delivery of genetic drugs, chemotherapeutic drugs, and anti-inflammatory drugs. As a genetic drug carrier, exosomes are beneficial to improve transfection efficiency and weaken side effects at the same time. Here, we use genetic engin...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8438888/ https://www.ncbi.nlm.nih.gov/pubmed/34521413 http://dx.doi.org/10.1186/s12935-021-02157-7 |
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author | Zhou, Wen Xu, Mingming Wang, Zhipeng Yang, Mingjun |
author_facet | Zhou, Wen Xu, Mingming Wang, Zhipeng Yang, Mingjun |
author_sort | Zhou, Wen |
collection | PubMed |
description | As an efficient drug carrier, exosome has been widely used in the delivery of genetic drugs, chemotherapeutic drugs, and anti-inflammatory drugs. As a genetic drug carrier, exosomes are beneficial to improve transfection efficiency and weaken side effects at the same time. Here, we use genetic engineering to prepare engineered exosomes (miR-449a Exo) that can actively deliver miR-449a. It was verified that miR-449a Exo had good homology targeting capacity and was specifically taken up by A549 cells. Moreover, miR-449a Exo had high delivery efficiency of miR-449a in vitro and in vivo. We demonstrated that miR-449a Exo effectively inhibited the proliferation of A549 cells and promoted their apoptosis. In addition, miR-449a Exo was found to control the progression of mouse tumors and prolong their survival in vivo. Our research provides new ideas for exosomes to efficiently and actively load gene drugs, and finds promising methods for the treatment of non-small cell lung cancer. |
format | Online Article Text |
id | pubmed-8438888 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-84388882021-09-14 Engineered exosomes loaded with miR-449a selectively inhibit the growth of homologous non-small cell lung cancer Zhou, Wen Xu, Mingming Wang, Zhipeng Yang, Mingjun Cancer Cell Int Primary Research As an efficient drug carrier, exosome has been widely used in the delivery of genetic drugs, chemotherapeutic drugs, and anti-inflammatory drugs. As a genetic drug carrier, exosomes are beneficial to improve transfection efficiency and weaken side effects at the same time. Here, we use genetic engineering to prepare engineered exosomes (miR-449a Exo) that can actively deliver miR-449a. It was verified that miR-449a Exo had good homology targeting capacity and was specifically taken up by A549 cells. Moreover, miR-449a Exo had high delivery efficiency of miR-449a in vitro and in vivo. We demonstrated that miR-449a Exo effectively inhibited the proliferation of A549 cells and promoted their apoptosis. In addition, miR-449a Exo was found to control the progression of mouse tumors and prolong their survival in vivo. Our research provides new ideas for exosomes to efficiently and actively load gene drugs, and finds promising methods for the treatment of non-small cell lung cancer. BioMed Central 2021-09-14 /pmc/articles/PMC8438888/ /pubmed/34521413 http://dx.doi.org/10.1186/s12935-021-02157-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Primary Research Zhou, Wen Xu, Mingming Wang, Zhipeng Yang, Mingjun Engineered exosomes loaded with miR-449a selectively inhibit the growth of homologous non-small cell lung cancer |
title | Engineered exosomes loaded with miR-449a selectively inhibit the growth of homologous non-small cell lung cancer |
title_full | Engineered exosomes loaded with miR-449a selectively inhibit the growth of homologous non-small cell lung cancer |
title_fullStr | Engineered exosomes loaded with miR-449a selectively inhibit the growth of homologous non-small cell lung cancer |
title_full_unstemmed | Engineered exosomes loaded with miR-449a selectively inhibit the growth of homologous non-small cell lung cancer |
title_short | Engineered exosomes loaded with miR-449a selectively inhibit the growth of homologous non-small cell lung cancer |
title_sort | engineered exosomes loaded with mir-449a selectively inhibit the growth of homologous non-small cell lung cancer |
topic | Primary Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8438888/ https://www.ncbi.nlm.nih.gov/pubmed/34521413 http://dx.doi.org/10.1186/s12935-021-02157-7 |
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