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Adult Stem Cell Functioning in the Tumor Micro-Environment
Tumor progression from an expanded cell population in a primary location to disseminated lethal growths subverts attempts at cures. It has become evident that these steps are driven in a large part by cancer cell-extrinsic signaling from the tumor microenvironment (TME), one cellular component of wh...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6566759/ https://www.ncbi.nlm.nih.gov/pubmed/31130595 http://dx.doi.org/10.3390/ijms20102566 |
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author | Jiang, Yuhan Wells, Alan Sylakowski, Kyle Clark, Amanda M. Ma, Bo |
author_facet | Jiang, Yuhan Wells, Alan Sylakowski, Kyle Clark, Amanda M. Ma, Bo |
author_sort | Jiang, Yuhan |
collection | PubMed |
description | Tumor progression from an expanded cell population in a primary location to disseminated lethal growths subverts attempts at cures. It has become evident that these steps are driven in a large part by cancer cell-extrinsic signaling from the tumor microenvironment (TME), one cellular component of which is becoming more appreciated for potential modulation of the cancer cells directly and the TME globally. That cell is a heterogenous population referred to as adult mesenchymal stem cells/multipotent stromal cells (MSCs). Herein, we review emerging evidence as to how these cells, both from distant sources, mainly the bone marrow, or local resident cells, can impact the progression of solid tumors. These nascent investigations raise more questions than they answer but paint a picture of an orchestrated web of signals and interactions that can be modulated to impact tumor progression. |
format | Online Article Text |
id | pubmed-6566759 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-65667592019-06-17 Adult Stem Cell Functioning in the Tumor Micro-Environment Jiang, Yuhan Wells, Alan Sylakowski, Kyle Clark, Amanda M. Ma, Bo Int J Mol Sci Review Tumor progression from an expanded cell population in a primary location to disseminated lethal growths subverts attempts at cures. It has become evident that these steps are driven in a large part by cancer cell-extrinsic signaling from the tumor microenvironment (TME), one cellular component of which is becoming more appreciated for potential modulation of the cancer cells directly and the TME globally. That cell is a heterogenous population referred to as adult mesenchymal stem cells/multipotent stromal cells (MSCs). Herein, we review emerging evidence as to how these cells, both from distant sources, mainly the bone marrow, or local resident cells, can impact the progression of solid tumors. These nascent investigations raise more questions than they answer but paint a picture of an orchestrated web of signals and interactions that can be modulated to impact tumor progression. MDPI 2019-05-25 /pmc/articles/PMC6566759/ /pubmed/31130595 http://dx.doi.org/10.3390/ijms20102566 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Jiang, Yuhan Wells, Alan Sylakowski, Kyle Clark, Amanda M. Ma, Bo Adult Stem Cell Functioning in the Tumor Micro-Environment |
title | Adult Stem Cell Functioning in the Tumor Micro-Environment |
title_full | Adult Stem Cell Functioning in the Tumor Micro-Environment |
title_fullStr | Adult Stem Cell Functioning in the Tumor Micro-Environment |
title_full_unstemmed | Adult Stem Cell Functioning in the Tumor Micro-Environment |
title_short | Adult Stem Cell Functioning in the Tumor Micro-Environment |
title_sort | adult stem cell functioning in the tumor micro-environment |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6566759/ https://www.ncbi.nlm.nih.gov/pubmed/31130595 http://dx.doi.org/10.3390/ijms20102566 |
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