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Actin stress fiber organization promotes cell stiffening and proliferation of pre-invasive breast cancer cells

Studies of the role of actin in tumour progression have highlighted its key contribution in cell softening associated with cell invasion. Here, using a human breast cell line with conditional Src induction, we demonstrate that cells undergo a stiffening state prior to acquiring malignant features. T...

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Autores principales: Tavares, Sandra, Vieira, André Filipe, Taubenberger, Anna Verena, Araújo, Margarida, Martins, Nuno Pimpao, Brás-Pereira, Catarina, Polónia, António, Herbig, Maik, Barreto, Clara, Otto, Oliver, Cardoso, Joana, Pereira-Leal, José B., Guck, Jochen, Paredes, Joana, Janody, Florence
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5440822/
https://www.ncbi.nlm.nih.gov/pubmed/28508872
http://dx.doi.org/10.1038/ncomms15237
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author Tavares, Sandra
Vieira, André Filipe
Taubenberger, Anna Verena
Araújo, Margarida
Martins, Nuno Pimpao
Brás-Pereira, Catarina
Polónia, António
Herbig, Maik
Barreto, Clara
Otto, Oliver
Cardoso, Joana
Pereira-Leal, José B.
Guck, Jochen
Paredes, Joana
Janody, Florence
author_facet Tavares, Sandra
Vieira, André Filipe
Taubenberger, Anna Verena
Araújo, Margarida
Martins, Nuno Pimpao
Brás-Pereira, Catarina
Polónia, António
Herbig, Maik
Barreto, Clara
Otto, Oliver
Cardoso, Joana
Pereira-Leal, José B.
Guck, Jochen
Paredes, Joana
Janody, Florence
author_sort Tavares, Sandra
collection PubMed
description Studies of the role of actin in tumour progression have highlighted its key contribution in cell softening associated with cell invasion. Here, using a human breast cell line with conditional Src induction, we demonstrate that cells undergo a stiffening state prior to acquiring malignant features. This state is characterized by the transient accumulation of stress fibres and upregulation of Ena/VASP-like (EVL). EVL, in turn, organizes stress fibres leading to transient cell stiffening, ERK-dependent cell proliferation, as well as enhancement of Src activation and progression towards a fully transformed state. Accordingly, EVL accumulates predominantly in premalignant breast lesions and is required for Src-induced epithelial overgrowth in Drosophila. While cell softening allows for cancer cell invasion, our work reveals that stress fibre-mediated cell stiffening could drive tumour growth during premalignant stages. A careful consideration of the mechanical properties of tumour cells could therefore offer new avenues of exploration when designing cancer-targeting therapies.
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spelling pubmed-54408222017-06-02 Actin stress fiber organization promotes cell stiffening and proliferation of pre-invasive breast cancer cells Tavares, Sandra Vieira, André Filipe Taubenberger, Anna Verena Araújo, Margarida Martins, Nuno Pimpao Brás-Pereira, Catarina Polónia, António Herbig, Maik Barreto, Clara Otto, Oliver Cardoso, Joana Pereira-Leal, José B. Guck, Jochen Paredes, Joana Janody, Florence Nat Commun Article Studies of the role of actin in tumour progression have highlighted its key contribution in cell softening associated with cell invasion. Here, using a human breast cell line with conditional Src induction, we demonstrate that cells undergo a stiffening state prior to acquiring malignant features. This state is characterized by the transient accumulation of stress fibres and upregulation of Ena/VASP-like (EVL). EVL, in turn, organizes stress fibres leading to transient cell stiffening, ERK-dependent cell proliferation, as well as enhancement of Src activation and progression towards a fully transformed state. Accordingly, EVL accumulates predominantly in premalignant breast lesions and is required for Src-induced epithelial overgrowth in Drosophila. While cell softening allows for cancer cell invasion, our work reveals that stress fibre-mediated cell stiffening could drive tumour growth during premalignant stages. A careful consideration of the mechanical properties of tumour cells could therefore offer new avenues of exploration when designing cancer-targeting therapies. Nature Publishing Group 2017-05-16 /pmc/articles/PMC5440822/ /pubmed/28508872 http://dx.doi.org/10.1038/ncomms15237 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Tavares, Sandra
Vieira, André Filipe
Taubenberger, Anna Verena
Araújo, Margarida
Martins, Nuno Pimpao
Brás-Pereira, Catarina
Polónia, António
Herbig, Maik
Barreto, Clara
Otto, Oliver
Cardoso, Joana
Pereira-Leal, José B.
Guck, Jochen
Paredes, Joana
Janody, Florence
Actin stress fiber organization promotes cell stiffening and proliferation of pre-invasive breast cancer cells
title Actin stress fiber organization promotes cell stiffening and proliferation of pre-invasive breast cancer cells
title_full Actin stress fiber organization promotes cell stiffening and proliferation of pre-invasive breast cancer cells
title_fullStr Actin stress fiber organization promotes cell stiffening and proliferation of pre-invasive breast cancer cells
title_full_unstemmed Actin stress fiber organization promotes cell stiffening and proliferation of pre-invasive breast cancer cells
title_short Actin stress fiber organization promotes cell stiffening and proliferation of pre-invasive breast cancer cells
title_sort actin stress fiber organization promotes cell stiffening and proliferation of pre-invasive breast cancer cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5440822/
https://www.ncbi.nlm.nih.gov/pubmed/28508872
http://dx.doi.org/10.1038/ncomms15237
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