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Human umbilical cord mesenchymal stem cell-derived extracellular vesicles promote lung adenocarcinoma growth by transferring miR-410
Although accumulating evidence has linked mesenchymal stem cells (MSCs) with tumor growth, the underlying mechanisms are poorly understood. Here, we demonstrated for the first time that human umbilical cord MSCs (hUCMSCs) dramatically increased the growth of lung adenocarcinoma (LUAD) cancer cells i...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5833395/ https://www.ncbi.nlm.nih.gov/pubmed/29440630 http://dx.doi.org/10.1038/s41419-018-0323-5 |
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author | Dong, Liyang Pu, Yanan Zhang, Lina Qi, Qianqian Xu, Lei Li, Wei Wei, Chuan Wang, Xiaofan Zhou, Sha Zhu, Jifeng Wang, Xuefeng Liu, Feng Chen, Xiaojun Su, Chuan |
author_facet | Dong, Liyang Pu, Yanan Zhang, Lina Qi, Qianqian Xu, Lei Li, Wei Wei, Chuan Wang, Xiaofan Zhou, Sha Zhu, Jifeng Wang, Xuefeng Liu, Feng Chen, Xiaojun Su, Chuan |
author_sort | Dong, Liyang |
collection | PubMed |
description | Although accumulating evidence has linked mesenchymal stem cells (MSCs) with tumor growth, the underlying mechanisms are poorly understood. Here, we demonstrated for the first time that human umbilical cord MSCs (hUCMSCs) dramatically increased the growth of lung adenocarcinoma (LUAD) cancer cells in a xenograft tumor model. Then, we observed that hUCMSC-derived extracellular vesicles (hUCMSC-EVs) contribute to the hUCMSC-promoted LUAD cell growth through a direct effect on LUAD cells. Furthermore, we showed that hUCMSC-EV-mediated LUAD growth is associated with increased proliferation and decreased apoptosis in LUAD cells, concomitant with reduced PTEN expression mediated by the hUCMSC-EV-transmitted miR-410. Our findings provide novel insights into the intercellular communications between cancer cells and MSCs through MSC-EV-miRNA and suggest that modification of hUCMSC-EVs might be an attractive therapeutic option for the clinical application of hUCMSC-EVs that would reduce unwanted side effects. |
format | Online Article Text |
id | pubmed-5833395 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58333952018-03-05 Human umbilical cord mesenchymal stem cell-derived extracellular vesicles promote lung adenocarcinoma growth by transferring miR-410 Dong, Liyang Pu, Yanan Zhang, Lina Qi, Qianqian Xu, Lei Li, Wei Wei, Chuan Wang, Xiaofan Zhou, Sha Zhu, Jifeng Wang, Xuefeng Liu, Feng Chen, Xiaojun Su, Chuan Cell Death Dis Article Although accumulating evidence has linked mesenchymal stem cells (MSCs) with tumor growth, the underlying mechanisms are poorly understood. Here, we demonstrated for the first time that human umbilical cord MSCs (hUCMSCs) dramatically increased the growth of lung adenocarcinoma (LUAD) cancer cells in a xenograft tumor model. Then, we observed that hUCMSC-derived extracellular vesicles (hUCMSC-EVs) contribute to the hUCMSC-promoted LUAD cell growth through a direct effect on LUAD cells. Furthermore, we showed that hUCMSC-EV-mediated LUAD growth is associated with increased proliferation and decreased apoptosis in LUAD cells, concomitant with reduced PTEN expression mediated by the hUCMSC-EV-transmitted miR-410. Our findings provide novel insights into the intercellular communications between cancer cells and MSCs through MSC-EV-miRNA and suggest that modification of hUCMSC-EVs might be an attractive therapeutic option for the clinical application of hUCMSC-EVs that would reduce unwanted side effects. Nature Publishing Group UK 2018-02-13 /pmc/articles/PMC5833395/ /pubmed/29440630 http://dx.doi.org/10.1038/s41419-018-0323-5 Text en © The Author(s) 2018 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Dong, Liyang Pu, Yanan Zhang, Lina Qi, Qianqian Xu, Lei Li, Wei Wei, Chuan Wang, Xiaofan Zhou, Sha Zhu, Jifeng Wang, Xuefeng Liu, Feng Chen, Xiaojun Su, Chuan Human umbilical cord mesenchymal stem cell-derived extracellular vesicles promote lung adenocarcinoma growth by transferring miR-410 |
title | Human umbilical cord mesenchymal stem cell-derived extracellular vesicles promote lung adenocarcinoma growth by transferring miR-410 |
title_full | Human umbilical cord mesenchymal stem cell-derived extracellular vesicles promote lung adenocarcinoma growth by transferring miR-410 |
title_fullStr | Human umbilical cord mesenchymal stem cell-derived extracellular vesicles promote lung adenocarcinoma growth by transferring miR-410 |
title_full_unstemmed | Human umbilical cord mesenchymal stem cell-derived extracellular vesicles promote lung adenocarcinoma growth by transferring miR-410 |
title_short | Human umbilical cord mesenchymal stem cell-derived extracellular vesicles promote lung adenocarcinoma growth by transferring miR-410 |
title_sort | human umbilical cord mesenchymal stem cell-derived extracellular vesicles promote lung adenocarcinoma growth by transferring mir-410 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5833395/ https://www.ncbi.nlm.nih.gov/pubmed/29440630 http://dx.doi.org/10.1038/s41419-018-0323-5 |
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