Mitosis can drive cell cannibalism through entosis

Author:

Durgan Joanne12,Tseng Yun-Yu23,Hamann Jens C24,Domart Marie-Charlotte5,Collinson Lucy5,Hall Alan2,Overholtzer Michael2,Florey Oliver1ORCID

Affiliation:

1. The Babraham Institute, Cambridge, United Kingdom

2. Memorial Sloan Kettering Cancer Center, New York, United States

3. Weill Graduate School of Medical Sciences, Cornell University, New York, United States

4. Louis V Gerstner Jr Graduate School of Biomedical Sciences, New York, United States

5. The Francis Crick Institute, London, United Kingdom

Abstract

Entosis is a form of epithelial cell cannibalism that is prevalent in human cancer, typically triggered by loss of matrix adhesion. Here, we report an alternative mechanism for entosis in human epithelial cells, driven by mitosis. Mitotic entosis is regulated by Cdc42, which controls mitotic morphology. Cdc42 depletion enhances mitotic deadhesion and rounding, and these biophysical changes, which depend on RhoA activation and are phenocopied by Rap1 inhibition, permit subsequent entosis. Mitotic entosis occurs constitutively in some human cancer cell lines and mitotic index correlates with cell cannibalism in primary human breast tumours. Adherent, wild-type cells can act efficiently as entotic hosts, suggesting that normal epithelia may engulf and kill aberrantly dividing neighbours. Finally, we report that Paclitaxel/taxol promotes mitotic rounding and subsequent entosis, revealing an unconventional activity of this drug. Together, our data uncover an intriguing link between cell division and cannibalism, of significance to both cancer and chemotherapy.

Funder

Cancer Research UK

Revson Senior Fellowship

Marie-Curie Fellowship

L'Oreal & UNESCO UK and Ireland

National Cancer Institute

Medical Research Council

Wellcome

Biotechnology and Biological Sciences Research Council

Engineering and Physical Sciences Research 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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