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Loss of polarity alters proliferation and differentiation in low-grade endometrial cancers by disrupting Notch signaling

Cell adhesion and apicobasal polarity together maintain epithelial tissue organization and homeostasis. Loss of adhesion has been described as a prerequisite for the epithelial to mesenchymal transition. However, what role misregulation of apicobasal polarity promotes tumor initiation and/or early p...

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Detalles Bibliográficos
Autores principales: Williams, Erin, Villar-Prados, Alejandro, Bowser, Jessica, Broaddus, Russell, Gladden, Andrew B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5716545/
https://www.ncbi.nlm.nih.gov/pubmed/29206870
http://dx.doi.org/10.1371/journal.pone.0189081
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author Williams, Erin
Villar-Prados, Alejandro
Bowser, Jessica
Broaddus, Russell
Gladden, Andrew B.
author_facet Williams, Erin
Villar-Prados, Alejandro
Bowser, Jessica
Broaddus, Russell
Gladden, Andrew B.
author_sort Williams, Erin
collection PubMed
description Cell adhesion and apicobasal polarity together maintain epithelial tissue organization and homeostasis. Loss of adhesion has been described as a prerequisite for the epithelial to mesenchymal transition. However, what role misregulation of apicobasal polarity promotes tumor initiation and/or early progression remains unclear. We find that human low-grade endometrial cancers are associated with disrupted localization of the apical polarity protein Par3 and Ezrin while, the adhesion molecule E-cadherin remains unchanged, accompanied by decreased Notch signaling, and altered Notch receptor localization. Depletion of Par3 or Ezrin, in a cell-based model, results in loss of epithelial architecture, differentiation, increased proliferation, migration and decreased Notch signaling. Re-expression of Par3 in endometrial cancer cell lines with disrupted Par3 protein levels blocks proliferation and reduces migration in a Notch dependent manner. These data uncover a function for apicobasal polarity independent of cell adhesion in regulating Notch-mediated differentiation signals in endometrial epithelial cells.
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spelling pubmed-57165452017-12-15 Loss of polarity alters proliferation and differentiation in low-grade endometrial cancers by disrupting Notch signaling Williams, Erin Villar-Prados, Alejandro Bowser, Jessica Broaddus, Russell Gladden, Andrew B. PLoS One Research Article Cell adhesion and apicobasal polarity together maintain epithelial tissue organization and homeostasis. Loss of adhesion has been described as a prerequisite for the epithelial to mesenchymal transition. However, what role misregulation of apicobasal polarity promotes tumor initiation and/or early progression remains unclear. We find that human low-grade endometrial cancers are associated with disrupted localization of the apical polarity protein Par3 and Ezrin while, the adhesion molecule E-cadherin remains unchanged, accompanied by decreased Notch signaling, and altered Notch receptor localization. Depletion of Par3 or Ezrin, in a cell-based model, results in loss of epithelial architecture, differentiation, increased proliferation, migration and decreased Notch signaling. Re-expression of Par3 in endometrial cancer cell lines with disrupted Par3 protein levels blocks proliferation and reduces migration in a Notch dependent manner. These data uncover a function for apicobasal polarity independent of cell adhesion in regulating Notch-mediated differentiation signals in endometrial epithelial cells. Public Library of Science 2017-12-05 /pmc/articles/PMC5716545/ /pubmed/29206870 http://dx.doi.org/10.1371/journal.pone.0189081 Text en © 2017 Williams et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Williams, Erin
Villar-Prados, Alejandro
Bowser, Jessica
Broaddus, Russell
Gladden, Andrew B.
Loss of polarity alters proliferation and differentiation in low-grade endometrial cancers by disrupting Notch signaling
title Loss of polarity alters proliferation and differentiation in low-grade endometrial cancers by disrupting Notch signaling
title_full Loss of polarity alters proliferation and differentiation in low-grade endometrial cancers by disrupting Notch signaling
title_fullStr Loss of polarity alters proliferation and differentiation in low-grade endometrial cancers by disrupting Notch signaling
title_full_unstemmed Loss of polarity alters proliferation and differentiation in low-grade endometrial cancers by disrupting Notch signaling
title_short Loss of polarity alters proliferation and differentiation in low-grade endometrial cancers by disrupting Notch signaling
title_sort loss of polarity alters proliferation and differentiation in low-grade endometrial cancers by disrupting notch signaling
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5716545/
https://www.ncbi.nlm.nih.gov/pubmed/29206870
http://dx.doi.org/10.1371/journal.pone.0189081
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