aPKCi triggers basal extrusion of luminal mammary epithelial cells by tuning contractility and vinculin localization at cell junctions.


Journal

Proceedings of the National Academy of Sciences of the United States of America
ISSN: 1091-6490
Titre abrégé: Proc Natl Acad Sci U S A
Pays: United States
ID NLM: 7505876

Informations de publication

Date de publication:
26 11 2019
Historique:
pubmed: 9 11 2019
medline: 23 4 2020
entrez: 9 11 2019
Statut: ppublish

Résumé

Metastasis is the main cause of cancer-related deaths. How a single oncogenic cell evolves within highly organized epithelium is still unknown. Here, we found that the overexpression of the protein kinase atypical protein kinase C ι (aPKCi), an oncogene, triggers basally oriented epithelial cell extrusion in vivo as a potential mechanism for early breast tumor cell invasion. We found that cell segregation is the first step required for basal extrusion of luminal cells and identify aPKCi and vinculin as regulators of cell segregation. We propose that asymmetric vinculin levels at the junction between normal and aPKCi

Identifiants

pubmed: 31699818
pii: 1906779116
doi: 10.1073/pnas.1906779116
pmc: PMC6883778
doi:

Substances chimiques

Isoenzymes 0
Vinculin 125361-02-6
Protein Kinase C EC 2.7.11.13
protein kinase C lambda EC 2.7.11.13

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

24108-24114

Informations de copyright

Copyright © 2019 the Author(s). Published by PNAS.

Déclaration de conflit d'intérêts

The authors declare no competing interest.

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Auteurs

Clémentine Villeneuve (C)

Institut Curie, Paris Université Sciences et Lettres, Sorbonne Université, CNRS, UMR144, 75005 Paris, France.

Emilie Lagoutte (E)

Institut Curie, Paris Université Sciences et Lettres, Sorbonne Université, CNRS, UMR144, 75005 Paris, France.

Ludmilla de Plater (L)

Institut Curie, Paris Université Sciences et Lettres, Sorbonne Université, CNRS UMR3215, INSERM U934, 75005 Paris, France.

Samuel Mathieu (S)

Institut Curie, Paris Université Sciences et Lettres, Sorbonne Université, CNRS, UMR144, 75005 Paris, France.

Jean-Baptiste Manneville (JB)

Institut Curie, Paris Université Sciences et Lettres, Sorbonne Université, CNRS, UMR144, 75005 Paris, France.

Jean-Léon Maître (JL)

Institut Curie, Paris Université Sciences et Lettres, Sorbonne Université, CNRS UMR3215, INSERM U934, 75005 Paris, France.

Philippe Chavrier (P)

Institut Curie, Paris Université Sciences et Lettres, Sorbonne Université, CNRS, UMR144, 75005 Paris, France.

Carine Rossé (C)

Institut Curie, Paris Université Sciences et Lettres, Sorbonne Université, CNRS, UMR144, 75005 Paris, France; carine.rosse@curie.fr.

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Classifications MeSH