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Hysteresis control of epithelial-mesenchymal transition dynamics conveys a distinct program with enhanced metastatic ability

Epithelial-mesenchymal transition (EMT) have been extensively characterized in development and cancer, and its dynamics have been modeled as a non-linear process. However, less is known about how such dynamics may affect its biological impact. Here, we use mathematical modeling and experimental anal...

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Autores principales: Celià-Terrassa, Toni, Bastian, Caleb, Liu, Daniel D., Ell, Brian, Aiello, Nicole M., Wei, Yong, Zamalloa, Jose, Blanco, Andres M., Hang, Xiang, Kunisky, Dmitriy, Li, Wenyang, Williams, Elizabeth D., Rabitz, Herschel, Kang, Yibin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6258667/
https://www.ncbi.nlm.nih.gov/pubmed/30479345
http://dx.doi.org/10.1038/s41467-018-07538-7
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author Celià-Terrassa, Toni
Bastian, Caleb
Liu, Daniel D.
Ell, Brian
Aiello, Nicole M.
Wei, Yong
Zamalloa, Jose
Blanco, Andres M.
Hang, Xiang
Kunisky, Dmitriy
Li, Wenyang
Williams, Elizabeth D.
Rabitz, Herschel
Kang, Yibin
author_facet Celià-Terrassa, Toni
Bastian, Caleb
Liu, Daniel D.
Ell, Brian
Aiello, Nicole M.
Wei, Yong
Zamalloa, Jose
Blanco, Andres M.
Hang, Xiang
Kunisky, Dmitriy
Li, Wenyang
Williams, Elizabeth D.
Rabitz, Herschel
Kang, Yibin
author_sort Celià-Terrassa, Toni
collection PubMed
description Epithelial-mesenchymal transition (EMT) have been extensively characterized in development and cancer, and its dynamics have been modeled as a non-linear process. However, less is known about how such dynamics may affect its biological impact. Here, we use mathematical modeling and experimental analysis of the TGF-β-induced EMT to reveal a non-linear hysteretic response of E-cadherin repression tightly controlled by the strength of the miR-200s/ZEBs negative feedback loop. Hysteretic EMT conveys memory state, ensures rapid and robust cellular response and enables EMT to persist long after withdrawal of stimuli. Importantly, while both hysteretic and non-hysteretic EMT confer similar morphological changes and invasive potential of cancer cells, only hysteretic EMT enhances lung metastatic colonization efficiency. Cells that undergo hysteretic EMT differentially express subsets of stem cell and extracellular matrix related genes with significant clinical prognosis value. These findings illustrate distinct biological impact of EMT depending on the dynamics of the transition.
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spelling pubmed-62586672018-11-29 Hysteresis control of epithelial-mesenchymal transition dynamics conveys a distinct program with enhanced metastatic ability Celià-Terrassa, Toni Bastian, Caleb Liu, Daniel D. Ell, Brian Aiello, Nicole M. Wei, Yong Zamalloa, Jose Blanco, Andres M. Hang, Xiang Kunisky, Dmitriy Li, Wenyang Williams, Elizabeth D. Rabitz, Herschel Kang, Yibin Nat Commun Article Epithelial-mesenchymal transition (EMT) have been extensively characterized in development and cancer, and its dynamics have been modeled as a non-linear process. However, less is known about how such dynamics may affect its biological impact. Here, we use mathematical modeling and experimental analysis of the TGF-β-induced EMT to reveal a non-linear hysteretic response of E-cadherin repression tightly controlled by the strength of the miR-200s/ZEBs negative feedback loop. Hysteretic EMT conveys memory state, ensures rapid and robust cellular response and enables EMT to persist long after withdrawal of stimuli. Importantly, while both hysteretic and non-hysteretic EMT confer similar morphological changes and invasive potential of cancer cells, only hysteretic EMT enhances lung metastatic colonization efficiency. Cells that undergo hysteretic EMT differentially express subsets of stem cell and extracellular matrix related genes with significant clinical prognosis value. These findings illustrate distinct biological impact of EMT depending on the dynamics of the transition. Nature Publishing Group UK 2018-11-27 /pmc/articles/PMC6258667/ /pubmed/30479345 http://dx.doi.org/10.1038/s41467-018-07538-7 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Celià-Terrassa, Toni
Bastian, Caleb
Liu, Daniel D.
Ell, Brian
Aiello, Nicole M.
Wei, Yong
Zamalloa, Jose
Blanco, Andres M.
Hang, Xiang
Kunisky, Dmitriy
Li, Wenyang
Williams, Elizabeth D.
Rabitz, Herschel
Kang, Yibin
Hysteresis control of epithelial-mesenchymal transition dynamics conveys a distinct program with enhanced metastatic ability
title Hysteresis control of epithelial-mesenchymal transition dynamics conveys a distinct program with enhanced metastatic ability
title_full Hysteresis control of epithelial-mesenchymal transition dynamics conveys a distinct program with enhanced metastatic ability
title_fullStr Hysteresis control of epithelial-mesenchymal transition dynamics conveys a distinct program with enhanced metastatic ability
title_full_unstemmed Hysteresis control of epithelial-mesenchymal transition dynamics conveys a distinct program with enhanced metastatic ability
title_short Hysteresis control of epithelial-mesenchymal transition dynamics conveys a distinct program with enhanced metastatic ability
title_sort hysteresis control of epithelial-mesenchymal transition dynamics conveys a distinct program with enhanced metastatic ability
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6258667/
https://www.ncbi.nlm.nih.gov/pubmed/30479345
http://dx.doi.org/10.1038/s41467-018-07538-7
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