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Exosomes derived from microRNA-584 transfected mesenchymal stem cells: novel alternative therapeutic vehicles for cancer therapy
Exosomes are small membranous vesicles which contain abundant RNA molecules, and are transferred from releasing cells to uptaking cells. MicroRNA (miRNA) is one of the transferred molecules affecting the adopted cells, including glioma cells. We hypothesized that mesenchymal stem cells (MSCs) can se...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Society for Biochemistry and Molecular Biology
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6130835/ https://www.ncbi.nlm.nih.gov/pubmed/29966581 http://dx.doi.org/10.5483/BMBRep.2018.51.8.105 |
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author | Kim, Ran Lee, Seokyeon Lee, Jihyun Kim, Minji Kim, Won Jung Lee, Hee Won Lee, Min Young Kim, Jongmin Chang, Woochul |
author_facet | Kim, Ran Lee, Seokyeon Lee, Jihyun Kim, Minji Kim, Won Jung Lee, Hee Won Lee, Min Young Kim, Jongmin Chang, Woochul |
author_sort | Kim, Ran |
collection | PubMed |
description | Exosomes are small membranous vesicles which contain abundant RNA molecules, and are transferred from releasing cells to uptaking cells. MicroRNA (miRNA) is one of the transferred molecules affecting the adopted cells, including glioma cells. We hypothesized that mesenchymal stem cells (MSCs) can secrete exosomes loading miRNA and have important effects on the progress of gliomas. To determine these effects by treating exosomal miRNA in culture media of miRNA mimic transfected MSCs, we assessed the in vitro cell proliferation and invasion capabilities, and the expression level of relative proteins associated with cell apoptosis, growth and migration. For animal studies, the mice injected with U87 cells were exposed to exosomes derived from miRNA-584-5p transfected MSCs, to confirm the influence of exosomal miRNA on the progress of glioma. Based on our results, we propose a new targeted cancer therapy wherein exosomes derived from miRNA transfected MSCs could be used to modulate tumor progress as the anticancer vehicles. |
format | Online Article Text |
id | pubmed-6130835 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Korean Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-61308352018-09-12 Exosomes derived from microRNA-584 transfected mesenchymal stem cells: novel alternative therapeutic vehicles for cancer therapy Kim, Ran Lee, Seokyeon Lee, Jihyun Kim, Minji Kim, Won Jung Lee, Hee Won Lee, Min Young Kim, Jongmin Chang, Woochul BMB Rep Articles Exosomes are small membranous vesicles which contain abundant RNA molecules, and are transferred from releasing cells to uptaking cells. MicroRNA (miRNA) is one of the transferred molecules affecting the adopted cells, including glioma cells. We hypothesized that mesenchymal stem cells (MSCs) can secrete exosomes loading miRNA and have important effects on the progress of gliomas. To determine these effects by treating exosomal miRNA in culture media of miRNA mimic transfected MSCs, we assessed the in vitro cell proliferation and invasion capabilities, and the expression level of relative proteins associated with cell apoptosis, growth and migration. For animal studies, the mice injected with U87 cells were exposed to exosomes derived from miRNA-584-5p transfected MSCs, to confirm the influence of exosomal miRNA on the progress of glioma. Based on our results, we propose a new targeted cancer therapy wherein exosomes derived from miRNA transfected MSCs could be used to modulate tumor progress as the anticancer vehicles. Korean Society for Biochemistry and Molecular Biology 2018-08 2018-08-31 /pmc/articles/PMC6130835/ /pubmed/29966581 http://dx.doi.org/10.5483/BMBRep.2018.51.8.105 Text en Copyright © 2018 by the The Korean Society for Biochemistry and Molecular Biology This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://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 | Articles Kim, Ran Lee, Seokyeon Lee, Jihyun Kim, Minji Kim, Won Jung Lee, Hee Won Lee, Min Young Kim, Jongmin Chang, Woochul Exosomes derived from microRNA-584 transfected mesenchymal stem cells: novel alternative therapeutic vehicles for cancer therapy |
title | Exosomes derived from microRNA-584 transfected mesenchymal stem cells: novel alternative therapeutic vehicles for cancer therapy |
title_full | Exosomes derived from microRNA-584 transfected mesenchymal stem cells: novel alternative therapeutic vehicles for cancer therapy |
title_fullStr | Exosomes derived from microRNA-584 transfected mesenchymal stem cells: novel alternative therapeutic vehicles for cancer therapy |
title_full_unstemmed | Exosomes derived from microRNA-584 transfected mesenchymal stem cells: novel alternative therapeutic vehicles for cancer therapy |
title_short | Exosomes derived from microRNA-584 transfected mesenchymal stem cells: novel alternative therapeutic vehicles for cancer therapy |
title_sort | exosomes derived from microrna-584 transfected mesenchymal stem cells: novel alternative therapeutic vehicles for cancer therapy |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6130835/ https://www.ncbi.nlm.nih.gov/pubmed/29966581 http://dx.doi.org/10.5483/BMBRep.2018.51.8.105 |
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