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The cancer glycocalyx mediates intravascular adhesion and extravasation during metastatic dissemination
The glycocalyx on tumor cells has been recently identified as an important driver for cancer progression, possibly providing critical opportunities for treatment. Metastasis, in particular, is often the limiting step in the survival to cancer, yet our understanding of how tumor cells escape the vasc...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7910477/ https://www.ncbi.nlm.nih.gov/pubmed/33637851 http://dx.doi.org/10.1038/s42003-021-01774-2 |
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author | Offeddu, Giovanni S. Hajal, Cynthia Foley, Colleen R. Wan, Zhengpeng Ibrahim, Lina Coughlin, Mark F. Kamm, Roger D. |
author_facet | Offeddu, Giovanni S. Hajal, Cynthia Foley, Colleen R. Wan, Zhengpeng Ibrahim, Lina Coughlin, Mark F. Kamm, Roger D. |
author_sort | Offeddu, Giovanni S. |
collection | PubMed |
description | The glycocalyx on tumor cells has been recently identified as an important driver for cancer progression, possibly providing critical opportunities for treatment. Metastasis, in particular, is often the limiting step in the survival to cancer, yet our understanding of how tumor cells escape the vascular system to initiate metastatic sites remains limited. Using an in vitro model of the human microvasculature, we assess here the importance of the tumor and vascular glycocalyces during tumor cell extravasation. Through selective manipulation of individual components of the glycocalyx, we reveal a mechanism whereby tumor cells prepare an adhesive vascular niche by depositing components of the glycocalyx along the endothelium. Accumulated hyaluronic acid shed by tumor cells subsequently mediates adhesion to the endothelium via the glycoprotein CD44. Trans-endothelial migration and invasion into the stroma occurs through binding of the isoform CD44v to components of the sub-endothelial extra-cellular matrix. Targeting of the hyaluronic acid-CD44 glycocalyx complex results in significant reduction in the extravasation of tumor cells. These studies provide evidence of tumor cells repurposing the glycocalyx to promote adhesive interactions leading to cancer progression. Such glycocalyx-mediated mechanisms may be therapeutically targeted to hinder metastasis and improve patient survival. |
format | Online Article Text |
id | pubmed-7910477 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79104772021-03-04 The cancer glycocalyx mediates intravascular adhesion and extravasation during metastatic dissemination Offeddu, Giovanni S. Hajal, Cynthia Foley, Colleen R. Wan, Zhengpeng Ibrahim, Lina Coughlin, Mark F. Kamm, Roger D. Commun Biol Article The glycocalyx on tumor cells has been recently identified as an important driver for cancer progression, possibly providing critical opportunities for treatment. Metastasis, in particular, is often the limiting step in the survival to cancer, yet our understanding of how tumor cells escape the vascular system to initiate metastatic sites remains limited. Using an in vitro model of the human microvasculature, we assess here the importance of the tumor and vascular glycocalyces during tumor cell extravasation. Through selective manipulation of individual components of the glycocalyx, we reveal a mechanism whereby tumor cells prepare an adhesive vascular niche by depositing components of the glycocalyx along the endothelium. Accumulated hyaluronic acid shed by tumor cells subsequently mediates adhesion to the endothelium via the glycoprotein CD44. Trans-endothelial migration and invasion into the stroma occurs through binding of the isoform CD44v to components of the sub-endothelial extra-cellular matrix. Targeting of the hyaluronic acid-CD44 glycocalyx complex results in significant reduction in the extravasation of tumor cells. These studies provide evidence of tumor cells repurposing the glycocalyx to promote adhesive interactions leading to cancer progression. Such glycocalyx-mediated mechanisms may be therapeutically targeted to hinder metastasis and improve patient survival. Nature Publishing Group UK 2021-02-26 /pmc/articles/PMC7910477/ /pubmed/33637851 http://dx.doi.org/10.1038/s42003-021-01774-2 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Offeddu, Giovanni S. Hajal, Cynthia Foley, Colleen R. Wan, Zhengpeng Ibrahim, Lina Coughlin, Mark F. Kamm, Roger D. The cancer glycocalyx mediates intravascular adhesion and extravasation during metastatic dissemination |
title | The cancer glycocalyx mediates intravascular adhesion and extravasation during metastatic dissemination |
title_full | The cancer glycocalyx mediates intravascular adhesion and extravasation during metastatic dissemination |
title_fullStr | The cancer glycocalyx mediates intravascular adhesion and extravasation during metastatic dissemination |
title_full_unstemmed | The cancer glycocalyx mediates intravascular adhesion and extravasation during metastatic dissemination |
title_short | The cancer glycocalyx mediates intravascular adhesion and extravasation during metastatic dissemination |
title_sort | cancer glycocalyx mediates intravascular adhesion and extravasation during metastatic dissemination |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7910477/ https://www.ncbi.nlm.nih.gov/pubmed/33637851 http://dx.doi.org/10.1038/s42003-021-01774-2 |
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