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Cancer-associated fibroblasts induce metalloprotease-independent cancer cell invasion of the basement membrane

At the stage of carcinoma in situ, the basement membrane (BM) segregates tumor cells from the stroma. This barrier must be breached to allow dissemination of the tumor cells to adjacent tissues. Cancer cells can perforate the BM using proteolysis; however, whether stromal cells play a role in this p...

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Autores principales: Glentis, Alexandros, Oertle, Philipp, Mariani, Pascale, Chikina, Aleksandra, El Marjou, Fatima, Attieh, Youmna, Zaccarini, Francois, Lae, Marick, Loew, Damarys, Dingli, Florent, Sirven, Philemon, Schoumacher, Marie, Gurchenkov, Basile G., Plodinec, Marija, Vignjevic, Danijela Matic
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5640679/
https://www.ncbi.nlm.nih.gov/pubmed/29030636
http://dx.doi.org/10.1038/s41467-017-00985-8
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author Glentis, Alexandros
Oertle, Philipp
Mariani, Pascale
Chikina, Aleksandra
El Marjou, Fatima
Attieh, Youmna
Zaccarini, Francois
Lae, Marick
Loew, Damarys
Dingli, Florent
Sirven, Philemon
Schoumacher, Marie
Gurchenkov, Basile G.
Plodinec, Marija
Vignjevic, Danijela Matic
author_facet Glentis, Alexandros
Oertle, Philipp
Mariani, Pascale
Chikina, Aleksandra
El Marjou, Fatima
Attieh, Youmna
Zaccarini, Francois
Lae, Marick
Loew, Damarys
Dingli, Florent
Sirven, Philemon
Schoumacher, Marie
Gurchenkov, Basile G.
Plodinec, Marija
Vignjevic, Danijela Matic
author_sort Glentis, Alexandros
collection PubMed
description At the stage of carcinoma in situ, the basement membrane (BM) segregates tumor cells from the stroma. This barrier must be breached to allow dissemination of the tumor cells to adjacent tissues. Cancer cells can perforate the BM using proteolysis; however, whether stromal cells play a role in this process remains unknown. Here we show that an abundant stromal cell population, cancer-associated fibroblasts (CAFs), promote cancer cell invasion through the BM. CAFs facilitate the breaching of the BM in a matrix metalloproteinase-independent manner. Instead, CAFs pull, stretch, and soften the BM leading to the formation of gaps through which cancer cells can migrate. By exerting contractile forces, CAFs alter the organization and the physical properties of the BM, making it permissive for cancer cell invasion. Blocking the ability of stromal cells to exert mechanical forces on the BM could therefore represent a new therapeutic strategy against aggressive tumors.
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spelling pubmed-56406792017-10-18 Cancer-associated fibroblasts induce metalloprotease-independent cancer cell invasion of the basement membrane Glentis, Alexandros Oertle, Philipp Mariani, Pascale Chikina, Aleksandra El Marjou, Fatima Attieh, Youmna Zaccarini, Francois Lae, Marick Loew, Damarys Dingli, Florent Sirven, Philemon Schoumacher, Marie Gurchenkov, Basile G. Plodinec, Marija Vignjevic, Danijela Matic Nat Commun Article At the stage of carcinoma in situ, the basement membrane (BM) segregates tumor cells from the stroma. This barrier must be breached to allow dissemination of the tumor cells to adjacent tissues. Cancer cells can perforate the BM using proteolysis; however, whether stromal cells play a role in this process remains unknown. Here we show that an abundant stromal cell population, cancer-associated fibroblasts (CAFs), promote cancer cell invasion through the BM. CAFs facilitate the breaching of the BM in a matrix metalloproteinase-independent manner. Instead, CAFs pull, stretch, and soften the BM leading to the formation of gaps through which cancer cells can migrate. By exerting contractile forces, CAFs alter the organization and the physical properties of the BM, making it permissive for cancer cell invasion. Blocking the ability of stromal cells to exert mechanical forces on the BM could therefore represent a new therapeutic strategy against aggressive tumors. Nature Publishing Group UK 2017-10-13 /pmc/articles/PMC5640679/ /pubmed/29030636 http://dx.doi.org/10.1038/s41467-017-00985-8 Text en © The Author(s) 2017 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
Glentis, Alexandros
Oertle, Philipp
Mariani, Pascale
Chikina, Aleksandra
El Marjou, Fatima
Attieh, Youmna
Zaccarini, Francois
Lae, Marick
Loew, Damarys
Dingli, Florent
Sirven, Philemon
Schoumacher, Marie
Gurchenkov, Basile G.
Plodinec, Marija
Vignjevic, Danijela Matic
Cancer-associated fibroblasts induce metalloprotease-independent cancer cell invasion of the basement membrane
title Cancer-associated fibroblasts induce metalloprotease-independent cancer cell invasion of the basement membrane
title_full Cancer-associated fibroblasts induce metalloprotease-independent cancer cell invasion of the basement membrane
title_fullStr Cancer-associated fibroblasts induce metalloprotease-independent cancer cell invasion of the basement membrane
title_full_unstemmed Cancer-associated fibroblasts induce metalloprotease-independent cancer cell invasion of the basement membrane
title_short Cancer-associated fibroblasts induce metalloprotease-independent cancer cell invasion of the basement membrane
title_sort cancer-associated fibroblasts induce metalloprotease-independent cancer cell invasion of the basement membrane
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5640679/
https://www.ncbi.nlm.nih.gov/pubmed/29030636
http://dx.doi.org/10.1038/s41467-017-00985-8
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