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Double‐edged sword of mesenchymal stem cells: Cancer‐promoting versus therapeutic potential

Mesenchymal stem cells (MSCs) derived from adipose tissue, bone marrow, cord blood, and other tissues, have recently attracted much attention as potential therapeutic agents in various diseases because of their trans‐differentiation capacity. However, recent studies have suggested that MSCs also app...

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Detalles Bibliográficos
Autores principales: Lee, Hwa‐Yong, Hong, In‐Sun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5623746/
https://www.ncbi.nlm.nih.gov/pubmed/28756624
http://dx.doi.org/10.1111/cas.13334
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author Lee, Hwa‐Yong
Hong, In‐Sun
author_facet Lee, Hwa‐Yong
Hong, In‐Sun
author_sort Lee, Hwa‐Yong
collection PubMed
description Mesenchymal stem cells (MSCs) derived from adipose tissue, bone marrow, cord blood, and other tissues, have recently attracted much attention as potential therapeutic agents in various diseases because of their trans‐differentiation capacity. However, recent studies have suggested that MSCs also appear to contribute to tumor pathogenesis by supporting tumor microenvironments, increasing tumor growth, and eliciting antitumor immune responses. Although some studies suggest that MSCs have inhibitory effects on tumor development, they are overwhelmed by a number of studies showing that MSCs exert stimulatory effects on tumor pathogenesis. In the present review, we summarize a number of findings to provide current information about the therapeutic potential of MSCs in various diseases. We then discuss the potential roles of MSCs in tumor progression.
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spelling pubmed-56237462017-10-04 Double‐edged sword of mesenchymal stem cells: Cancer‐promoting versus therapeutic potential Lee, Hwa‐Yong Hong, In‐Sun Cancer Sci Review Articles Mesenchymal stem cells (MSCs) derived from adipose tissue, bone marrow, cord blood, and other tissues, have recently attracted much attention as potential therapeutic agents in various diseases because of their trans‐differentiation capacity. However, recent studies have suggested that MSCs also appear to contribute to tumor pathogenesis by supporting tumor microenvironments, increasing tumor growth, and eliciting antitumor immune responses. Although some studies suggest that MSCs have inhibitory effects on tumor development, they are overwhelmed by a number of studies showing that MSCs exert stimulatory effects on tumor pathogenesis. In the present review, we summarize a number of findings to provide current information about the therapeutic potential of MSCs in various diseases. We then discuss the potential roles of MSCs in tumor progression. John Wiley and Sons Inc. 2017-08-29 2017-10 /pmc/articles/PMC5623746/ /pubmed/28756624 http://dx.doi.org/10.1111/cas.13334 Text en © 2017 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Review Articles
Lee, Hwa‐Yong
Hong, In‐Sun
Double‐edged sword of mesenchymal stem cells: Cancer‐promoting versus therapeutic potential
title Double‐edged sword of mesenchymal stem cells: Cancer‐promoting versus therapeutic potential
title_full Double‐edged sword of mesenchymal stem cells: Cancer‐promoting versus therapeutic potential
title_fullStr Double‐edged sword of mesenchymal stem cells: Cancer‐promoting versus therapeutic potential
title_full_unstemmed Double‐edged sword of mesenchymal stem cells: Cancer‐promoting versus therapeutic potential
title_short Double‐edged sword of mesenchymal stem cells: Cancer‐promoting versus therapeutic potential
title_sort double‐edged sword of mesenchymal stem cells: cancer‐promoting versus therapeutic potential
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5623746/
https://www.ncbi.nlm.nih.gov/pubmed/28756624
http://dx.doi.org/10.1111/cas.13334
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