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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...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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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. |
format | Online Article Text |
id | pubmed-5440822 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
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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