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Physical Biology in Cancer. 3. The role of cell glycocalyx in vascular transport of circulating tumor cells

Circulating tumor cells (CTCs) in blood are known to adhere to the luminal surface of the microvasculature via receptor-mediated adhesion, which contributes to the spread of cancer metastasis to anatomically distant organs. Such interactions between ligands on CTCs and endothelial cell-bound surface...

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Detalles Bibliográficos
Autores principales: Mitchell, Michael J., King, Michael R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Physiological Society 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3919988/
https://www.ncbi.nlm.nih.gov/pubmed/24133067
http://dx.doi.org/10.1152/ajpcell.00285.2013
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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 Circulating tumor cells (CTCs) in blood are known to adhere to the luminal surface of the microvasculature via receptor-mediated adhesion, which contributes to the spread of cancer metastasis to anatomically distant organs. Such interactions between ligands on CTCs and endothelial cell-bound surface receptors are sensitive to receptor-ligand distances at the nanoscale. The sugar-rich coating expressed on the surface of CTCs and endothelial cells, known as the glycocalyx, serves as a physical structure that can control the spacing and, thus, the availability of such receptor-ligand interactions. The cancer cell glycocalyx can also regulate the ability of therapeutic ligands to bind to CTCs in the bloodstream. Here, we review the role of cell glycocalyx on the adhesion and therapeutic treatment of CTCs in the bloodstream.
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spelling pubmed-39199882014-02-11 Physical Biology in Cancer. 3. The role of cell glycocalyx in vascular transport of circulating tumor cells Mitchell, Michael J. King, Michael R. Am J Physiol Cell Physiol Themes Circulating tumor cells (CTCs) in blood are known to adhere to the luminal surface of the microvasculature via receptor-mediated adhesion, which contributes to the spread of cancer metastasis to anatomically distant organs. Such interactions between ligands on CTCs and endothelial cell-bound surface receptors are sensitive to receptor-ligand distances at the nanoscale. The sugar-rich coating expressed on the surface of CTCs and endothelial cells, known as the glycocalyx, serves as a physical structure that can control the spacing and, thus, the availability of such receptor-ligand interactions. The cancer cell glycocalyx can also regulate the ability of therapeutic ligands to bind to CTCs in the bloodstream. Here, we review the role of cell glycocalyx on the adhesion and therapeutic treatment of CTCs in the bloodstream. American Physiological Society 2013-10-16 2014-01-15 /pmc/articles/PMC3919988/ /pubmed/24133067 http://dx.doi.org/10.1152/ajpcell.00285.2013 Text en Copyright © 2014 the American Physiological Society Licensed under Creative Commons Attribution CC-BY 3.0 (http://creativecommons.org/licenses/by/3.0/deed.en_US) : The American Physiological Society.
spellingShingle Themes
Mitchell, Michael J.
King, Michael R.
Physical Biology in Cancer. 3. The role of cell glycocalyx in vascular transport of circulating tumor cells
title Physical Biology in Cancer. 3. The role of cell glycocalyx in vascular transport of circulating tumor cells
title_full Physical Biology in Cancer. 3. The role of cell glycocalyx in vascular transport of circulating tumor cells
title_fullStr Physical Biology in Cancer. 3. The role of cell glycocalyx in vascular transport of circulating tumor cells
title_full_unstemmed Physical Biology in Cancer. 3. The role of cell glycocalyx in vascular transport of circulating tumor cells
title_short Physical Biology in Cancer. 3. The role of cell glycocalyx in vascular transport of circulating tumor cells
title_sort physical biology in cancer. 3. the role of cell glycocalyx in vascular transport of circulating tumor cells
topic Themes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3919988/
https://www.ncbi.nlm.nih.gov/pubmed/24133067
http://dx.doi.org/10.1152/ajpcell.00285.2013
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