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Computational and Experimental Models of Cancer Cell Response to Fluid Shear Stress
It has become evident that mechanical forces play a key role in cancer metastasis, a complex series of steps that is responsible for the majority of cancer-related deaths. One such force is fluid shear stress, exerted on circulating tumor cells by blood flow in the vascular microenvironment, and als...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3587800/ https://www.ncbi.nlm.nih.gov/pubmed/23467856 http://dx.doi.org/10.3389/fonc.2013.00044 |
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author | Mitchell, Michael J. King, Michael R. |
author_facet | Mitchell, Michael J. King, Michael R. |
author_sort | Mitchell, Michael J. |
collection | PubMed |
description | It has become evident that mechanical forces play a key role in cancer metastasis, a complex series of steps that is responsible for the majority of cancer-related deaths. One such force is fluid shear stress, exerted on circulating tumor cells by blood flow in the vascular microenvironment, and also on tumor cells exposed to slow interstitial flows in the tumor microenvironment. Computational and experimental models have the potential to elucidate metastatic behavior of cells exposed to such forces. Here, we review the fluid-generated forces that tumor cells are exposed to in the vascular and tumor microenvironments, and discuss recent computational and experimental models that have revealed mechanotransduction phenomena that may play a role in the metastatic process. |
format | Online Article Text |
id | pubmed-3587800 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-35878002013-03-06 Computational and Experimental Models of Cancer Cell Response to Fluid Shear Stress Mitchell, Michael J. King, Michael R. Front Oncol Oncology It has become evident that mechanical forces play a key role in cancer metastasis, a complex series of steps that is responsible for the majority of cancer-related deaths. One such force is fluid shear stress, exerted on circulating tumor cells by blood flow in the vascular microenvironment, and also on tumor cells exposed to slow interstitial flows in the tumor microenvironment. Computational and experimental models have the potential to elucidate metastatic behavior of cells exposed to such forces. Here, we review the fluid-generated forces that tumor cells are exposed to in the vascular and tumor microenvironments, and discuss recent computational and experimental models that have revealed mechanotransduction phenomena that may play a role in the metastatic process. Frontiers Media S.A. 2013-03-05 /pmc/articles/PMC3587800/ /pubmed/23467856 http://dx.doi.org/10.3389/fonc.2013.00044 Text en Copyright © 2013 Mitchell and King. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc. |
spellingShingle | Oncology Mitchell, Michael J. King, Michael R. Computational and Experimental Models of Cancer Cell Response to Fluid Shear Stress |
title | Computational and Experimental Models of Cancer Cell Response to Fluid Shear Stress |
title_full | Computational and Experimental Models of Cancer Cell Response to Fluid Shear Stress |
title_fullStr | Computational and Experimental Models of Cancer Cell Response to Fluid Shear Stress |
title_full_unstemmed | Computational and Experimental Models of Cancer Cell Response to Fluid Shear Stress |
title_short | Computational and Experimental Models of Cancer Cell Response to Fluid Shear Stress |
title_sort | computational and experimental models of cancer cell response to fluid shear stress |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3587800/ https://www.ncbi.nlm.nih.gov/pubmed/23467856 http://dx.doi.org/10.3389/fonc.2013.00044 |
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