Confined migration promotes cancer metastasis through resistance to anoikis and increased invasiveness

Author:

Fanfone Deborah12,Wu Zhichong1345,Mammi Jade12,Berthenet Kevin124,Neves David6,Weber Kathrin12,Halaburkova Andrea12,Virard François17,Bunel Félix8,Jamard Catherine12,Hernandez-Vargas Hector149,Tait Stephen WG1011,Hennino Ana134,Ichim Gabriel12ORCID

Affiliation:

1. Cancer Research Center of Lyon (CRCL), INSERM 1052, CNRS

2. Cancer Cell Death Laboratory, part of LabEx DEVweCAN, Université de Lyon

3. Université Lyon 1, Villeurbanne

4. Centre Léon Bérard

5. Department of General Surgery, Pancreatic Disease Center, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine

6. Netris Pharma

7. Université Claude Bernard Lyon 1, Faculté d’Odontologie, Hospices Civils de Lyon

8. ENS de Lyon, Université Claude Bernard Lyon 1, CNRS, Laboratoire de Physique

9. Université Claude Bernard Lyon 1

10. Cancer Research UK Beatson Institute

11. Institute of Cancer Sciences, University of Glasgow

Abstract

Mechanical stress is known to fuel several hallmarks of cancer, ranging from genome instability to uncontrolled proliferation or invasion. Cancer cells are constantly challenged by mechanical stresses not only in the primary tumour but also during metastasis. However, this latter has seldom been studied with regards to mechanobiology, in particular resistance to anoikis, a cell death programme triggered by loss of cell adhesion. Here, we show in vitro that migrating breast cancer cells develop resistance to anoikis following their passage through microporous membranes mimicking confined migration (CM), a mechanical constriction that cancer cells encounter during metastasis. This CM-induced resistance was mediated by Inhibitory of Apoptosis Proteins, and sensitivity to anoikis could be restored after their inhibition using second mitochondria-derived activator of caspase (SMAC) mimetics. Anoikis-resistant mechanically stressed cancer cells displayed enhanced cell motility and evasion from natural killer cell-mediated immune surveillance, as well as a marked advantage to form lung metastatic lesions in mice. Our findings reveal that CM increases the metastatic potential of breast cancer cells.

Funder

Agence Nationale de la Recherche

Ligue Nationale Contre le Cancer

Fondation de France

French National Cancer Institute

Centre Léon Bérard

China Scholarship Council

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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