Author
Listed:
- Sandra Tavares
(Instituto Gulbenkian de Ciência, Rua da Quinta Grande 6)
- André Filipe Vieira
(Epithelial Interactions in Cancer group, Instituto de Investigação e Inovação em Saúde (i3S), Universidade do Porto
Cancer Genetics group, Instituto de Patologia e Imunologia Molecular da Universidade do Porto (Ipatimup))
- Anna Verena Taubenberger
(Biotechnology Center, Technische Universität Dresden)
- Margarida Araújo
(Instituto Gulbenkian de Ciência, Rua da Quinta Grande 6)
- Nuno Pimpao Martins
(Instituto Gulbenkian de Ciência, Rua da Quinta Grande 6)
- Catarina Brás-Pereira
(Instituto Gulbenkian de Ciência, Rua da Quinta Grande 6)
- António Polónia
(Epithelial Interactions in Cancer group, Instituto de Investigação e Inovação em Saúde (i3S), Universidade do Porto
Cancer Genetics group, Instituto de Patologia e Imunologia Molecular da Universidade do Porto (Ipatimup)
Ipatimup Diagnostics)
- Maik Herbig
(Biotechnology Center, Technische Universität Dresden)
- Clara Barreto
(Instituto Gulbenkian de Ciência, Rua da Quinta Grande 6)
- Oliver Otto
(Biotechnology Center, Technische Universität Dresden)
- Joana Cardoso
(Instituto Gulbenkian de Ciência, Rua da Quinta Grande 6
Ophiomics—Precision Medicine, Rua Cupertino de Miranda 9, lote 8)
- José B. Pereira-Leal
(Instituto Gulbenkian de Ciência, Rua da Quinta Grande 6
Ophiomics—Precision Medicine, Rua Cupertino de Miranda 9, lote 8)
- Jochen Guck
(Biotechnology Center, Technische Universität Dresden)
- Joana Paredes
(Epithelial Interactions in Cancer group, Instituto de Investigação e Inovação em Saúde (i3S), Universidade do Porto
Cancer Genetics group, Instituto de Patologia e Imunologia Molecular da Universidade do Porto (Ipatimup)
Faculty of Medicine, University of Porto)
- Florence Janody
(Instituto Gulbenkian de Ciência, Rua da Quinta Grande 6)
Abstract
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.
Suggested Citation
Sandra Tavares & André Filipe Vieira & Anna Verena Taubenberger & Margarida Araújo & Nuno Pimpao Martins & Catarina Brás-Pereira & António Polónia & Maik Herbig & Clara Barreto & Oliver Otto & Joana C, 2017.
"Actin stress fiber organization promotes cell stiffening and proliferation of pre-invasive breast cancer cells,"
Nature Communications, Nature, vol. 8(1), pages 1-18, August.
Handle:
RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_ncomms15237
DOI: 10.1038/ncomms15237
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Citations
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Cited by:
- Song Gao & Shuaibin Wang & Zhiying Zhao & Chao Zhang & Zhicao Liu & Ping Ye & Zhifang Xu & Baozhu Yi & Kai Jiao & Gurudatta A. Naik & Shi Wei & Soroush Rais-Bahrami & Sejong Bae & Wei-Hsiung Yang & Gu, 2022.
"TUBB4A interacts with MYH9 to protect the nucleus during cell migration and promotes prostate cancer via GSK3β/β-catenin signalling,"
Nature Communications, Nature, vol. 13(1), pages 1-16, December.
- Qin, Xing & Hu, Jianhua & Ma, Shuangge & Wu, Mengyun, 2024.
"Estimation of multiple networks with common structures in heterogeneous subgroups,"
Journal of Multivariate Analysis, Elsevier, vol. 202(C).
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