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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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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. |
format | Online Article Text |
id | pubmed-6258667 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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