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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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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. |
format | Online Article Text |
id | pubmed-5716545 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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