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EMT and MET: necessary or permissive for metastasis?

Epithelial‐to‐mesenchymal transition (EMT) and its reverse mesenchymal‐to‐epithelial transition (MET) have been suggested to play crucial roles in metastatic dissemination of carcinomas. These phenotypic transitions between states are not binary. Instead, carcinoma cells often exhibit a spectrum of...

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Autores principales: Jolly, Mohit Kumar, Ware, Kathryn E., Gilja, Shivee, Somarelli, Jason A., Levine, Herbert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5496498/
https://www.ncbi.nlm.nih.gov/pubmed/28548345
http://dx.doi.org/10.1002/1878-0261.12083
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author Jolly, Mohit Kumar
Ware, Kathryn E.
Gilja, Shivee
Somarelli, Jason A.
Levine, Herbert
author_facet Jolly, Mohit Kumar
Ware, Kathryn E.
Gilja, Shivee
Somarelli, Jason A.
Levine, Herbert
author_sort Jolly, Mohit Kumar
collection PubMed
description Epithelial‐to‐mesenchymal transition (EMT) and its reverse mesenchymal‐to‐epithelial transition (MET) have been suggested to play crucial roles in metastatic dissemination of carcinomas. These phenotypic transitions between states are not binary. Instead, carcinoma cells often exhibit a spectrum of epithelial/mesenchymal phenotype(s). While epithelial/mesenchymal plasticity has been observed preclinically and clinically, whether any of these phenotypic transitions are indispensable for metastatic outgrowth remains an unanswered question. Here, we focus on epithelial/mesenchymal plasticity in metastatic dissemination and propose alternative mechanisms for successful dissemination and metastases beyond the traditional EMT/MET view. We highlight multiple hypotheses that can help reconcile conflicting observations, and outline the next set of key questions that can offer valuable insights into mechanisms of metastasis in multiple tumor models.
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spelling pubmed-54964982017-07-18 EMT and MET: necessary or permissive for metastasis? Jolly, Mohit Kumar Ware, Kathryn E. Gilja, Shivee Somarelli, Jason A. Levine, Herbert Mol Oncol Reviews Epithelial‐to‐mesenchymal transition (EMT) and its reverse mesenchymal‐to‐epithelial transition (MET) have been suggested to play crucial roles in metastatic dissemination of carcinomas. These phenotypic transitions between states are not binary. Instead, carcinoma cells often exhibit a spectrum of epithelial/mesenchymal phenotype(s). While epithelial/mesenchymal plasticity has been observed preclinically and clinically, whether any of these phenotypic transitions are indispensable for metastatic outgrowth remains an unanswered question. Here, we focus on epithelial/mesenchymal plasticity in metastatic dissemination and propose alternative mechanisms for successful dissemination and metastases beyond the traditional EMT/MET view. We highlight multiple hypotheses that can help reconcile conflicting observations, and outline the next set of key questions that can offer valuable insights into mechanisms of metastasis in multiple tumor models. John Wiley and Sons Inc. 2017-06-12 2017-07 /pmc/articles/PMC5496498/ /pubmed/28548345 http://dx.doi.org/10.1002/1878-0261.12083 Text en © 2017 The Authors. Published by FEBS Press and John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Reviews
Jolly, Mohit Kumar
Ware, Kathryn E.
Gilja, Shivee
Somarelli, Jason A.
Levine, Herbert
EMT and MET: necessary or permissive for metastasis?
title EMT and MET: necessary or permissive for metastasis?
title_full EMT and MET: necessary or permissive for metastasis?
title_fullStr EMT and MET: necessary or permissive for metastasis?
title_full_unstemmed EMT and MET: necessary or permissive for metastasis?
title_short EMT and MET: necessary or permissive for metastasis?
title_sort emt and met: necessary or permissive for metastasis?
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5496498/
https://www.ncbi.nlm.nih.gov/pubmed/28548345
http://dx.doi.org/10.1002/1878-0261.12083
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