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Role of cancer-associated mesenchymal stem cells in the tumor microenvironment: A review

Mesenchymal stem cells (MSCs) were applied to the therapy for degenerative diseases, immune, and inflammation. In tumor microenvironments (TME), different sources of MSCs showed that tumor-promoting and -inhibiting effects were mediated by different signaling pathways. Cancer-associated MSCs (CaMSCs...

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Detalles Bibliográficos
Autores principales: Wang, Kai-Hung, Ding, Dah-Ching
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9972927/
https://www.ncbi.nlm.nih.gov/pubmed/36866340
http://dx.doi.org/10.4103/tcmj.tcmj_138_22
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author Wang, Kai-Hung
Ding, Dah-Ching
author_facet Wang, Kai-Hung
Ding, Dah-Ching
author_sort Wang, Kai-Hung
collection PubMed
description Mesenchymal stem cells (MSCs) were applied to the therapy for degenerative diseases, immune, and inflammation. In tumor microenvironments (TME), different sources of MSCs showed that tumor-promoting and -inhibiting effects were mediated by different signaling pathways. Cancer-associated MSCs (CaMSCs) could be recruited from bone marrow or local tissues and mainly showed tumor-promoting and immunosuppressive effects. The transformed CaMSCs preserve the characteristics of stem cells, but the properties of regulating TME are different. Hence, we specifically focus on CaMSCs and discuss the detailed mechanisms of regulating the development of cancer cells and immune cells. CaMSCs could be a potential therapeutic target in various types of cancer. However, the detailed mechanisms of CaMSCs in the TME are relatively less known and need further study.
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spelling pubmed-99729272023-03-01 Role of cancer-associated mesenchymal stem cells in the tumor microenvironment: A review Wang, Kai-Hung Ding, Dah-Ching Tzu Chi Med J Review Article Mesenchymal stem cells (MSCs) were applied to the therapy for degenerative diseases, immune, and inflammation. In tumor microenvironments (TME), different sources of MSCs showed that tumor-promoting and -inhibiting effects were mediated by different signaling pathways. Cancer-associated MSCs (CaMSCs) could be recruited from bone marrow or local tissues and mainly showed tumor-promoting and immunosuppressive effects. The transformed CaMSCs preserve the characteristics of stem cells, but the properties of regulating TME are different. Hence, we specifically focus on CaMSCs and discuss the detailed mechanisms of regulating the development of cancer cells and immune cells. CaMSCs could be a potential therapeutic target in various types of cancer. However, the detailed mechanisms of CaMSCs in the TME are relatively less known and need further study. Wolters Kluwer - Medknow 2022-08-01 /pmc/articles/PMC9972927/ /pubmed/36866340 http://dx.doi.org/10.4103/tcmj.tcmj_138_22 Text en Copyright: © 2022 Tzu Chi Medical Journal https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Review Article
Wang, Kai-Hung
Ding, Dah-Ching
Role of cancer-associated mesenchymal stem cells in the tumor microenvironment: A review
title Role of cancer-associated mesenchymal stem cells in the tumor microenvironment: A review
title_full Role of cancer-associated mesenchymal stem cells in the tumor microenvironment: A review
title_fullStr Role of cancer-associated mesenchymal stem cells in the tumor microenvironment: A review
title_full_unstemmed Role of cancer-associated mesenchymal stem cells in the tumor microenvironment: A review
title_short Role of cancer-associated mesenchymal stem cells in the tumor microenvironment: A review
title_sort role of cancer-associated mesenchymal stem cells in the tumor microenvironment: a review
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9972927/
https://www.ncbi.nlm.nih.gov/pubmed/36866340
http://dx.doi.org/10.4103/tcmj.tcmj_138_22
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