Evidence map›Paper›PMID 39779939›Full record

ArticleNature cell biology2025

Chromosome mis-segregation triggers cell cycle arrest through a mechanosensitive nuclear envelope checkpoint.

Solène Hervé, Andrea Scelfo, Gabriele Bersano Marchisio, Marine Grison, Kotryna Vaidžiulytė, Marie Dumont, Annapaola Angrisani, Adib Keikhosravi, Gianluca Pegoraro, Mathieu Deygas and 8 more

Abstract read
In one paragraph

Article in Nature cell biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

29 citing papers in PubMed.

  1. Review
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  15. Cell confinement initiates a delayed but heritable loss of chromosomes.bioRxiv : the preprint server for biology · 2026
    Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. Stress transmission towards the nucleus of the cell.Frontiers in cell and developmental biology · 2026
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors.

Solène Hervé *CNRS UMR144 - UMR3664, Institut Curie, Sorbonne Université, PSL Research University, Paris, France.
Andrea Scelfo *CNRS UMR144 - UMR3664, Institut Curie, Sorbonne Université, PSL Research University, Paris, France.ORCID 0000-0001-8767-0688
Gabriele Bersano MarchisioCNRS UMR144 - UMR3664, Institut Curie, Sorbonne Université, PSL Research University, Paris, France.
Marine GrisonCNRS UMR144 - UMR3664, Institut Curie, Sorbonne Université, PSL Research University, Paris, France.
Kotryna VaidžiulytėCNRS UMR144, Institut Curie, Institut Pierre Gilles de Gennes, PSL Research University, Paris, France.
Marie DumontCNRS UMR144 - UMR3664, Institut Curie, Sorbonne Université, PSL Research University, Paris, France.
Annapaola AngrisaniCNRS UMR144 - UMR3664, Institut Curie, Sorbonne Université, PSL Research University, Paris, France.
Adib KeikhosraviHigh-Throughput Imaging Facility, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Gianluca PegoraroHigh-Throughput Imaging Facility, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.ORCID 0000-0003-2843-9464
Mathieu DeygasCNRS UMR144, Institut Curie, Institut Pierre Gilles de Gennes, PSL Research University, Paris, France.
Guilherme P F NaderCNRS UMR144, Institut Curie, Institut Pierre Gilles de Gennes, PSL Research University, Paris, France.
Anne-Sophie MacéCNRS UMR144 - UMR3664, Institut Curie, Sorbonne Université, PSL Research University, Paris, France.
Matteo GentiliINSERM U932, Institut Curie, PSL Research University, Paris, France.ORCID 0000-0002-6970-8133
Alice WilliartCNRS UMR144, Institut Curie, Institut Pierre Gilles de Gennes, PSL Research University, Paris, France.
Nicolas ManelINSERM U932, Institut Curie, PSL Research University, Paris, France.ORCID 0000-0002-1481-4430
Matthieu PielCNRS UMR144, Institut Curie, Institut Pierre Gilles de Gennes, PSL Research University, Paris, France.ORCID 0000-0002-2848-177X
Yekaterina A MiroshnikovaLaboratory of Molecular Biology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD, USA. yekaterina.miroshnikova@nih.gov.ORCID 0000-0001-9771-4963
Daniele FachinettiCNRS UMR144 - UMR3664, Institut Curie, Sorbonne Université, PSL Research University, Paris, France. daniele.fachinetti@curie.fr.ORCID 0000-0002-8795-6771

Funding

Associazione Italiana per la Ricerca sul Cancro (Italian Association for Cancer Research) 800924
6 · The paper itself

Abstract

Errors during cell division lead to aneuploidy, which is associated with genomic instability and cell transformation. In response to aneuploidy, cells activate the tumour suppressor p53 to elicit a surveillance mechanism that halts proliferation and promotes senescence. The molecular sensors that trigger this checkpoint are unclear. Here, using a tunable system of chromosome mis-segregation, we show that mitotic errors trigger nuclear deformation, nuclear softening, and lamin and heterochromatin alterations, leading to rapid p53/p21 activation upon mitotic exit in response to changes in nuclear mechanics. We identify mTORC2 and ATR as nuclear deformation sensors upstream of p53/p21 activation. While triggering mitotic arrest, the chromosome mis-segregation-induced alterations of nuclear envelope mechanics provide a fitness advantage for aneuploid cells by promoting nuclear deformation resilience and enhancing pro-invasive capabilities. Collectively, this work identifies a nuclear mechanical checkpoint triggered by altered chromatin organization that probably plays a critical role in cellular transformation and cancer progression.

Indexed as

Cell Cycle CheckpointsChromosome SegregationMechanotransduction, CellularNuclear EnvelopeAneuploidyAnimalsAtaxia Telangiectasia Mutated ProteinsCell Line, TumorHeterochromatinHumansMitosisTumor Suppressor Protein p53Ataxia Telangiectasia Mutated ProteinsATR protein, humanHeterochromatinTP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID39779939
PMCPMC11735390

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.