Evidence map›Paper›PMID 26783302›Full record

ArticleThe Journal of cell biology2016

P-cadherin promotes collective cell migration via a Cdc42-mediated increase in mechanical forces.

Cédric Plutoni, Elsa Bazellieres, Maïlys Le Borgne-Rochet, Franck Comunale, Agusti Brugues, Martial Séveno, Damien Planchon, Sylvie Thuault, Nathalie Morin, Stéphane Bodin and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
10.6field-weighted citation impact, top 1% of its field
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

63 citing papers in PubMed, 104 citations in OpenAlex.

  1. Article
  2. Review
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  4. Nuclear destabilisation - a possible genesis of cancer?Biological reviews of the Cambridge Philosophical Society · 2025
    Review
  5. E-Cadherin Is a Structuring Component of Invadopodia in Pancreatic Cancer.Journal of cellular and molecular medicine · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
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  12. Roles of the Dbl family of RhoGEFs in mechanotransduction - a review.Frontiers in cell and developmental biology · 2024
    Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
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  20. Article

3 more citing papers are in PubMed but not listed here.

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

12 authors at 4 institutions in 2 countries.

Cédric PlutoniCentre de Recherche de Biochimie Macromoléculaire, Centre National de la Recherche Scientifique, Unité Mixte de Recherche 5237, Universités Montpellier, 34293 Montpellier, France.
Elsa BazellieresInstitute for Bioengineering of Catalonia, Universitat de Barcelona, 08007 Barcelona, Spain.
Maïlys Le Borgne-RochetCentre de Recherche de Biochimie Macromoléculaire, Centre National de la Recherche Scientifique, Unité Mixte de Recherche 5237, Universités Montpellier, 34293 Montpellier, France.
Franck ComunaleCentre de Recherche de Biochimie Macromoléculaire, Centre National de la Recherche Scientifique, Unité Mixte de Recherche 5237, Universités Montpellier, 34293 Montpellier, France.
Agusti BruguesInstitute for Bioengineering of Catalonia, Universitat de Barcelona, 08007 Barcelona, Spain.
Martial SévenoFunctional Proteomics Platform, Institut de Génomique Fonctionnelle, Centre National de la Recherche Scientifique, Unité Mixte de Recherche 5203, Institut National de la Santé et de la Recherche Médicale U1191, Universités Montpellier, 34094 Montpellier, France.
Damien PlanchonCentre de Recherche de Biochimie Macromoléculaire, Centre National de la Recherche Scientifique, Unité Mixte de Recherche 5237, Universités Montpellier, 34293 Montpellier, France.
Sylvie ThuaultCentre de Recherche de Biochimie Macromoléculaire, Centre National de la Recherche Scientifique, Unité Mixte de Recherche 5237, Universités Montpellier, 34293 Montpellier, France.
Nathalie MorinCentre de Recherche de Biochimie Macromoléculaire, Centre National de la Recherche Scientifique, Unité Mixte de Recherche 5237, Universités Montpellier, 34293 Montpellier, France.
Stéphane BodinCentre de Recherche de Biochimie Macromoléculaire, Centre National de la Recherche Scientifique, Unité Mixte de Recherche 5237, Universités Montpellier, 34293 Montpellier, France.
Xavier TrepatInstitute for Bioengineering of Catalonia, Universitat de Barcelona, 08007 Barcelona, Spain Centro de Investigación Biomédica en Red en Bioingeniería, Biomateriales y Nanomedicina, 08010 Barcelona, Spain.
Cécile Gauthier-RouvièreCentre de Recherche de Biochimie Macromoléculaire, Centre National de la Recherche Scientifique, Unité Mixte de Recherche 5237, Universités Montpellier, 34293 Montpellier, France cecile.gauthier@crbm.cnrs.fr.
Centre de Recherche en Biologie cellulaire de Montpellier · FRInstitute for Bioengineering of Catalonia · ESBiomedical Research Networking Center in Bioengineering, Biomaterials and Nanomedicine · ESInserm · FR

Funding

European Research Council 242993
6 · The paper itself

Abstract

Collective cell migration (CCM) is essential for organism development, wound healing, and metastatic transition, the primary cause of cancer-related death, and it involves cell-cell adhesion molecules of the cadherin family. Increased P-cadherin expression levels are correlated with tumor aggressiveness in carcinoma and aggressive sarcoma; however, how P-cadherin promotes tumor malignancy remains unknown. Here, using integrated cell biology and biophysical approaches, we determined that P-cadherin specifically induces polarization and CCM through an increase in the strength and anisotropy of mechanical forces. We show that this mechanical regulation is mediated by the P-cadherin/β-PIX/Cdc42 axis; P-cadherin specifically activates Cdc42 through β-PIX, which is specifically recruited at cell-cell contacts upon CCM. This mechanism of cell polarization and migration is absent in cells expressing E- or R-cadherin. Thus, we identify a specific role of P-cadherin through β-PIX-mediated Cdc42 activation in the regulation of cell polarity and force anisotropy that drives CCM.

Indexed as

Cell MovementAnimalsBiomechanical PhenomenaCadherinscdc42 GTP-Binding ProteinCell PolarityCells, CulturedMiceMyoblastsRho Guanine Nucleotide Exchange FactorsArhgef7 protein, mouseCadherinscdc42 GTP-Binding ProteinCdc42 protein, mouseRho Guanine Nucleotide Exchange Factors

Identifiers

PMID26783302
PMCPMC4738379
OpenAlexW2278684209

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

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.