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Cell–cell adhesion: linking Wnt/β-catenin signaling with partial EMT and stemness traits in tumorigenesis

Changes in cell adhesion and motility are considered key elements in determining the development of invasive and metastatic tumors. Co-opting the epithelial-to-mesenchymal transition (EMT) process, which is known to occur during embryonic development, and the associated changes in cell adhesion prop...

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Detalles Bibliográficos
Autores principales: Basu, Sayon, Cheriyamundath, Sanith, Ben-Ze’ev, Avri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000 Research Limited 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6144947/
https://www.ncbi.nlm.nih.gov/pubmed/30271576
http://dx.doi.org/10.12688/f1000research.15782.1
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author Basu, Sayon
Cheriyamundath, Sanith
Ben-Ze’ev, Avri
author_facet Basu, Sayon
Cheriyamundath, Sanith
Ben-Ze’ev, Avri
author_sort Basu, Sayon
collection PubMed
description Changes in cell adhesion and motility are considered key elements in determining the development of invasive and metastatic tumors. Co-opting the epithelial-to-mesenchymal transition (EMT) process, which is known to occur during embryonic development, and the associated changes in cell adhesion properties in cancer cells are considered major routes for tumor progression. More recent in vivo studies in tumor tissues and circulating tumor cell clusters suggest a stepwise EMT process rather than an “all-or-none” transition during tumor progression. In this commentary, we addressed the molecular mechanisms underlying the changes in cell adhesion and motility and adhesion-mediated signaling and their relationships to the partial EMT states and the acquisition of stemness traits by cancer cells.
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spelling pubmed-61449472018-09-27 Cell–cell adhesion: linking Wnt/β-catenin signaling with partial EMT and stemness traits in tumorigenesis Basu, Sayon Cheriyamundath, Sanith Ben-Ze’ev, Avri F1000Res Review Changes in cell adhesion and motility are considered key elements in determining the development of invasive and metastatic tumors. Co-opting the epithelial-to-mesenchymal transition (EMT) process, which is known to occur during embryonic development, and the associated changes in cell adhesion properties in cancer cells are considered major routes for tumor progression. More recent in vivo studies in tumor tissues and circulating tumor cell clusters suggest a stepwise EMT process rather than an “all-or-none” transition during tumor progression. In this commentary, we addressed the molecular mechanisms underlying the changes in cell adhesion and motility and adhesion-mediated signaling and their relationships to the partial EMT states and the acquisition of stemness traits by cancer cells. F1000 Research Limited 2018-09-18 /pmc/articles/PMC6144947/ /pubmed/30271576 http://dx.doi.org/10.12688/f1000research.15782.1 Text en Copyright: © 2018 Basu S et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Basu, Sayon
Cheriyamundath, Sanith
Ben-Ze’ev, Avri
Cell–cell adhesion: linking Wnt/β-catenin signaling with partial EMT and stemness traits in tumorigenesis
title Cell–cell adhesion: linking Wnt/β-catenin signaling with partial EMT and stemness traits in tumorigenesis
title_full Cell–cell adhesion: linking Wnt/β-catenin signaling with partial EMT and stemness traits in tumorigenesis
title_fullStr Cell–cell adhesion: linking Wnt/β-catenin signaling with partial EMT and stemness traits in tumorigenesis
title_full_unstemmed Cell–cell adhesion: linking Wnt/β-catenin signaling with partial EMT and stemness traits in tumorigenesis
title_short Cell–cell adhesion: linking Wnt/β-catenin signaling with partial EMT and stemness traits in tumorigenesis
title_sort cell–cell adhesion: linking wnt/β-catenin signaling with partial emt and stemness traits in tumorigenesis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6144947/
https://www.ncbi.nlm.nih.gov/pubmed/30271576
http://dx.doi.org/10.12688/f1000research.15782.1
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