Cargando…

Oncogenic Linear Collagen VI of Invasive Breast Cancer Is Induced by CCL5

The triple-negative breast tumor boundary is made of aligned, linear collagen. The pro-oncogenic impact of linear collagen is well established; however, its mechanism of formation is unknown. An in vitro analogue of the tumor border is created by a co-culture of MDA-MB-231 cells, adipose derived ste...

Descripción completa

Detalles Bibliográficos
Autores principales: Brett, Elizabeth, Sauter, Matthias, Timmins, Éadaoin, Azimzadeh, Omid, Rosemann, Michael, Merl-Pham, Juliane, Hauck, Stefanie M., Nelson, Peter J., Becker, Karl Friedrich, Schunn, Ilse, Lowery, Aoife, Kerin, Michael J., Atkinson, Michael, Krüger, Achim, Machens, Hans-Günther, Duscher, Dominik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7230614/
https://www.ncbi.nlm.nih.gov/pubmed/32252260
http://dx.doi.org/10.3390/jcm9040991
_version_ 1783534995708575744
author Brett, Elizabeth
Sauter, Matthias
Timmins, Éadaoin
Azimzadeh, Omid
Rosemann, Michael
Merl-Pham, Juliane
Hauck, Stefanie M.
Nelson, Peter J.
Becker, Karl Friedrich
Schunn, Ilse
Lowery, Aoife
Kerin, Michael J.
Atkinson, Michael
Krüger, Achim
Machens, Hans-Günther
Duscher, Dominik
author_facet Brett, Elizabeth
Sauter, Matthias
Timmins, Éadaoin
Azimzadeh, Omid
Rosemann, Michael
Merl-Pham, Juliane
Hauck, Stefanie M.
Nelson, Peter J.
Becker, Karl Friedrich
Schunn, Ilse
Lowery, Aoife
Kerin, Michael J.
Atkinson, Michael
Krüger, Achim
Machens, Hans-Günther
Duscher, Dominik
author_sort Brett, Elizabeth
collection PubMed
description The triple-negative breast tumor boundary is made of aligned, linear collagen. The pro-oncogenic impact of linear collagen is well established; however, its mechanism of formation is unknown. An in vitro analogue of the tumor border is created by a co-culture of MDA-MB-231 cells, adipose derived stem cells, and dermal fibroblasts. Decellularization of this co-culture after seven days reveals an extracellular matrix that is linear in fashion, high in pro-oncogenic collagen type VI, and able to promote invasion of reseeded cells. Further investigation revealed linear collagen VI is produced by fibroblasts in response to a paracrine co-culture of adipose derived stem cells and MDA-MB-231, which together secrete high levels of the chemokine CCL5. The addition of monoclonal antibody against CCL5 to the co-culture results in an unorganized matrix with dramatically decreased collagen VI. Importantly, reseeded cells do not exhibit pro-oncogenic behavior. These data illustrate a cellular mechanism, which creates linear extracellular matrix (ECM) in vitro, and highlight a potential role of CCL5 for building striated tumor collagen in vivo.
format Online
Article
Text
id pubmed-7230614
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-72306142020-05-22 Oncogenic Linear Collagen VI of Invasive Breast Cancer Is Induced by CCL5 Brett, Elizabeth Sauter, Matthias Timmins, Éadaoin Azimzadeh, Omid Rosemann, Michael Merl-Pham, Juliane Hauck, Stefanie M. Nelson, Peter J. Becker, Karl Friedrich Schunn, Ilse Lowery, Aoife Kerin, Michael J. Atkinson, Michael Krüger, Achim Machens, Hans-Günther Duscher, Dominik J Clin Med Article The triple-negative breast tumor boundary is made of aligned, linear collagen. The pro-oncogenic impact of linear collagen is well established; however, its mechanism of formation is unknown. An in vitro analogue of the tumor border is created by a co-culture of MDA-MB-231 cells, adipose derived stem cells, and dermal fibroblasts. Decellularization of this co-culture after seven days reveals an extracellular matrix that is linear in fashion, high in pro-oncogenic collagen type VI, and able to promote invasion of reseeded cells. Further investigation revealed linear collagen VI is produced by fibroblasts in response to a paracrine co-culture of adipose derived stem cells and MDA-MB-231, which together secrete high levels of the chemokine CCL5. The addition of monoclonal antibody against CCL5 to the co-culture results in an unorganized matrix with dramatically decreased collagen VI. Importantly, reseeded cells do not exhibit pro-oncogenic behavior. These data illustrate a cellular mechanism, which creates linear extracellular matrix (ECM) in vitro, and highlight a potential role of CCL5 for building striated tumor collagen in vivo. MDPI 2020-04-02 /pmc/articles/PMC7230614/ /pubmed/32252260 http://dx.doi.org/10.3390/jcm9040991 Text en © 2020 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 Article
Brett, Elizabeth
Sauter, Matthias
Timmins, Éadaoin
Azimzadeh, Omid
Rosemann, Michael
Merl-Pham, Juliane
Hauck, Stefanie M.
Nelson, Peter J.
Becker, Karl Friedrich
Schunn, Ilse
Lowery, Aoife
Kerin, Michael J.
Atkinson, Michael
Krüger, Achim
Machens, Hans-Günther
Duscher, Dominik
Oncogenic Linear Collagen VI of Invasive Breast Cancer Is Induced by CCL5
title Oncogenic Linear Collagen VI of Invasive Breast Cancer Is Induced by CCL5
title_full Oncogenic Linear Collagen VI of Invasive Breast Cancer Is Induced by CCL5
title_fullStr Oncogenic Linear Collagen VI of Invasive Breast Cancer Is Induced by CCL5
title_full_unstemmed Oncogenic Linear Collagen VI of Invasive Breast Cancer Is Induced by CCL5
title_short Oncogenic Linear Collagen VI of Invasive Breast Cancer Is Induced by CCL5
title_sort oncogenic linear collagen vi of invasive breast cancer is induced by ccl5
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7230614/
https://www.ncbi.nlm.nih.gov/pubmed/32252260
http://dx.doi.org/10.3390/jcm9040991
work_keys_str_mv AT brettelizabeth oncogeniclinearcollagenviofinvasivebreastcancerisinducedbyccl5
AT sautermatthias oncogeniclinearcollagenviofinvasivebreastcancerisinducedbyccl5
AT timminseadaoin oncogeniclinearcollagenviofinvasivebreastcancerisinducedbyccl5
AT azimzadehomid oncogeniclinearcollagenviofinvasivebreastcancerisinducedbyccl5
AT rosemannmichael oncogeniclinearcollagenviofinvasivebreastcancerisinducedbyccl5
AT merlphamjuliane oncogeniclinearcollagenviofinvasivebreastcancerisinducedbyccl5
AT hauckstefaniem oncogeniclinearcollagenviofinvasivebreastcancerisinducedbyccl5
AT nelsonpeterj oncogeniclinearcollagenviofinvasivebreastcancerisinducedbyccl5
AT beckerkarlfriedrich oncogeniclinearcollagenviofinvasivebreastcancerisinducedbyccl5
AT schunnilse oncogeniclinearcollagenviofinvasivebreastcancerisinducedbyccl5
AT loweryaoife oncogeniclinearcollagenviofinvasivebreastcancerisinducedbyccl5
AT kerinmichaelj oncogeniclinearcollagenviofinvasivebreastcancerisinducedbyccl5
AT atkinsonmichael oncogeniclinearcollagenviofinvasivebreastcancerisinducedbyccl5
AT krugerachim oncogeniclinearcollagenviofinvasivebreastcancerisinducedbyccl5
AT machenshansgunther oncogeniclinearcollagenviofinvasivebreastcancerisinducedbyccl5
AT duscherdominik oncogeniclinearcollagenviofinvasivebreastcancerisinducedbyccl5