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Stromal cells regulate mechanics of tumour spheroid

The remarkable contractility and force generation ability exhibited by cancer cells empower them to overcome the resistance and steric hindrance presented by a three-dimensional, interconnected matrix. Cancer cells disseminate by actively remodelling and deforming their extracellular matrix (ECM). T...

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Autores principales: Agrawal, Ayushi, Lasli, Soufian, Javanmardi, Yousef, Coursier, Diane, Micalet, Auxtine, Watson, Sara, Shahreza, Somayeh, Serwinski, Bianca, Djordjevic, Boris, Szita, Nicolas, Cheema, Umber, Bertazzo, Sergio, Calvo, Fernando, Moeendarbary, Emad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10585335/
https://www.ncbi.nlm.nih.gov/pubmed/37868949
http://dx.doi.org/10.1016/j.mtbio.2023.100821
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author Agrawal, Ayushi
Lasli, Soufian
Javanmardi, Yousef
Coursier, Diane
Micalet, Auxtine
Watson, Sara
Shahreza, Somayeh
Serwinski, Bianca
Djordjevic, Boris
Szita, Nicolas
Cheema, Umber
Bertazzo, Sergio
Calvo, Fernando
Moeendarbary, Emad
author_facet Agrawal, Ayushi
Lasli, Soufian
Javanmardi, Yousef
Coursier, Diane
Micalet, Auxtine
Watson, Sara
Shahreza, Somayeh
Serwinski, Bianca
Djordjevic, Boris
Szita, Nicolas
Cheema, Umber
Bertazzo, Sergio
Calvo, Fernando
Moeendarbary, Emad
author_sort Agrawal, Ayushi
collection PubMed
description The remarkable contractility and force generation ability exhibited by cancer cells empower them to overcome the resistance and steric hindrance presented by a three-dimensional, interconnected matrix. Cancer cells disseminate by actively remodelling and deforming their extracellular matrix (ECM). The process of tumour growth and its ECM remodelling have been extensively studied, but the effect of the cellular tumour microenvironment (TME) has been ignored in most studies that investigated tumour-cell-mediated ECM deformations and realignment. This study reports the integration of stromal cells in spheroid contractility assays that impacts the ECM remodelling and invasion abilities of cancer spheroids. To investigate this, we developed a novel multilayer in vitro assay that incorporates stromal cells and quantifies the contractile deformations that tumour spheroids exert on the ECM. We observed a negative correlation between the spheroid invasion potential and the levels of collagen deformation. The presence of stromal cells significantly increased cancer cell invasiveness and altered the cancer cells' ability to deform and realign collagen gel, due to upregulation of proinflammatory cytokines. Interestingly, this was observed consistently in both metastatic and non-metastatic cancer cells. Our findings contribute to a better understanding of the vital role played by the cellular TME in regulating the invasive outgrowth of cancer cells and underscore the potential of utilising matrix deformation measurements as a biophysical marker for evaluating invasiveness and informing targeted therapeutic opportunities.
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spelling pubmed-105853352023-10-20 Stromal cells regulate mechanics of tumour spheroid Agrawal, Ayushi Lasli, Soufian Javanmardi, Yousef Coursier, Diane Micalet, Auxtine Watson, Sara Shahreza, Somayeh Serwinski, Bianca Djordjevic, Boris Szita, Nicolas Cheema, Umber Bertazzo, Sergio Calvo, Fernando Moeendarbary, Emad Mater Today Bio Full Length Article The remarkable contractility and force generation ability exhibited by cancer cells empower them to overcome the resistance and steric hindrance presented by a three-dimensional, interconnected matrix. Cancer cells disseminate by actively remodelling and deforming their extracellular matrix (ECM). The process of tumour growth and its ECM remodelling have been extensively studied, but the effect of the cellular tumour microenvironment (TME) has been ignored in most studies that investigated tumour-cell-mediated ECM deformations and realignment. This study reports the integration of stromal cells in spheroid contractility assays that impacts the ECM remodelling and invasion abilities of cancer spheroids. To investigate this, we developed a novel multilayer in vitro assay that incorporates stromal cells and quantifies the contractile deformations that tumour spheroids exert on the ECM. We observed a negative correlation between the spheroid invasion potential and the levels of collagen deformation. The presence of stromal cells significantly increased cancer cell invasiveness and altered the cancer cells' ability to deform and realign collagen gel, due to upregulation of proinflammatory cytokines. Interestingly, this was observed consistently in both metastatic and non-metastatic cancer cells. Our findings contribute to a better understanding of the vital role played by the cellular TME in regulating the invasive outgrowth of cancer cells and underscore the potential of utilising matrix deformation measurements as a biophysical marker for evaluating invasiveness and informing targeted therapeutic opportunities. Elsevier 2023-10-06 /pmc/articles/PMC10585335/ /pubmed/37868949 http://dx.doi.org/10.1016/j.mtbio.2023.100821 Text en Crown Copyright © 2023 Published by Elsevier Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Full Length Article
Agrawal, Ayushi
Lasli, Soufian
Javanmardi, Yousef
Coursier, Diane
Micalet, Auxtine
Watson, Sara
Shahreza, Somayeh
Serwinski, Bianca
Djordjevic, Boris
Szita, Nicolas
Cheema, Umber
Bertazzo, Sergio
Calvo, Fernando
Moeendarbary, Emad
Stromal cells regulate mechanics of tumour spheroid
title Stromal cells regulate mechanics of tumour spheroid
title_full Stromal cells regulate mechanics of tumour spheroid
title_fullStr Stromal cells regulate mechanics of tumour spheroid
title_full_unstemmed Stromal cells regulate mechanics of tumour spheroid
title_short Stromal cells regulate mechanics of tumour spheroid
title_sort stromal cells regulate mechanics of tumour spheroid
topic Full Length Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10585335/
https://www.ncbi.nlm.nih.gov/pubmed/37868949
http://dx.doi.org/10.1016/j.mtbio.2023.100821
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