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Distinguishing mechanisms underlying EMT tristability
BACKGROUND: The Epithelial-Mesenchymal Transition (EMT) endows epithelial-looking cells with enhanced migratory ability during embryonic development and tissue repair. EMT can also be co-opted by cancer cells to acquire metastatic potential and drug-resistance. Recent research has argued that epithe...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5876698/ https://www.ncbi.nlm.nih.gov/pubmed/29623961 http://dx.doi.org/10.1186/s41236-017-0005-8 |
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author | Jia, Dongya Jolly, Mohit Kumar Tripathi, Satyendra C. Den Hollander, Petra Huang, Bin Lu, Mingyang Celiktas, Muge Ramirez-Peña, Esmeralda Ben-Jacob, Eshel Onuchic, José N. Hanash, Samir M. Mani, Sendurai A. Levine, Herbert |
author_facet | Jia, Dongya Jolly, Mohit Kumar Tripathi, Satyendra C. Den Hollander, Petra Huang, Bin Lu, Mingyang Celiktas, Muge Ramirez-Peña, Esmeralda Ben-Jacob, Eshel Onuchic, José N. Hanash, Samir M. Mani, Sendurai A. Levine, Herbert |
author_sort | Jia, Dongya |
collection | PubMed |
description | BACKGROUND: The Epithelial-Mesenchymal Transition (EMT) endows epithelial-looking cells with enhanced migratory ability during embryonic development and tissue repair. EMT can also be co-opted by cancer cells to acquire metastatic potential and drug-resistance. Recent research has argued that epithelial (E) cells can undergo either a partial EMT to attain a hybrid epithelial/mesenchymal (E/M) phenotype that typically displays collective migration, or a complete EMT to adopt a mesenchymal (M) phenotype that shows individual migration. The core EMT regulatory network - miR-34/SNAIL/miR-200/ZEB1 - has been identified by various studies, but how this network regulates the transitions among the E, E/M, and M phenotypes remains controversial. Two major mathematical models – ternary chimera switch (TCS) and cascading bistable switches (CBS) - that both focus on the miR-34/SNAIL/miR-200/ZEB1 network, have been proposed to elucidate the EMT dynamics, but a detailed analysis of how well either or both of these two models can capture recent experimental observations about EMT dynamics remains to be done. RESULTS: Here, via an integrated experimental and theoretical approach, we first show that both these two models can be used to understand the two-step transition of EMT - E→E/M→M, the different responses of SNAIL and ZEB1 to exogenous TGF-β and the irreversibility of complete EMT. Next, we present new experimental results that tend to discriminate between these two models. We show that ZEB1 is present at intermediate levels in the hybrid E/M H1975 cells, and that in HMLE cells, overexpression of SNAIL is not sufficient to initiate EMT in the absence of ZEB1 and FOXC2. CONCLUSIONS: These experimental results argue in favor of the TCS model proposing that miR-200/ZEB1 behaves as a three-way decision-making switch enabling transitions among the E, hybrid E/M and M phenotypes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s41236-017-0005-8) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5876698 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-58766982018-04-03 Distinguishing mechanisms underlying EMT tristability Jia, Dongya Jolly, Mohit Kumar Tripathi, Satyendra C. Den Hollander, Petra Huang, Bin Lu, Mingyang Celiktas, Muge Ramirez-Peña, Esmeralda Ben-Jacob, Eshel Onuchic, José N. Hanash, Samir M. Mani, Sendurai A. Levine, Herbert Cancer Converg Research BACKGROUND: The Epithelial-Mesenchymal Transition (EMT) endows epithelial-looking cells with enhanced migratory ability during embryonic development and tissue repair. EMT can also be co-opted by cancer cells to acquire metastatic potential and drug-resistance. Recent research has argued that epithelial (E) cells can undergo either a partial EMT to attain a hybrid epithelial/mesenchymal (E/M) phenotype that typically displays collective migration, or a complete EMT to adopt a mesenchymal (M) phenotype that shows individual migration. The core EMT regulatory network - miR-34/SNAIL/miR-200/ZEB1 - has been identified by various studies, but how this network regulates the transitions among the E, E/M, and M phenotypes remains controversial. Two major mathematical models – ternary chimera switch (TCS) and cascading bistable switches (CBS) - that both focus on the miR-34/SNAIL/miR-200/ZEB1 network, have been proposed to elucidate the EMT dynamics, but a detailed analysis of how well either or both of these two models can capture recent experimental observations about EMT dynamics remains to be done. RESULTS: Here, via an integrated experimental and theoretical approach, we first show that both these two models can be used to understand the two-step transition of EMT - E→E/M→M, the different responses of SNAIL and ZEB1 to exogenous TGF-β and the irreversibility of complete EMT. Next, we present new experimental results that tend to discriminate between these two models. We show that ZEB1 is present at intermediate levels in the hybrid E/M H1975 cells, and that in HMLE cells, overexpression of SNAIL is not sufficient to initiate EMT in the absence of ZEB1 and FOXC2. CONCLUSIONS: These experimental results argue in favor of the TCS model proposing that miR-200/ZEB1 behaves as a three-way decision-making switch enabling transitions among the E, hybrid E/M and M phenotypes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s41236-017-0005-8) contains supplementary material, which is available to authorized users. Springer International Publishing 2017-11-01 2017 /pmc/articles/PMC5876698/ /pubmed/29623961 http://dx.doi.org/10.1186/s41236-017-0005-8 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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. |
spellingShingle | Research Jia, Dongya Jolly, Mohit Kumar Tripathi, Satyendra C. Den Hollander, Petra Huang, Bin Lu, Mingyang Celiktas, Muge Ramirez-Peña, Esmeralda Ben-Jacob, Eshel Onuchic, José N. Hanash, Samir M. Mani, Sendurai A. Levine, Herbert Distinguishing mechanisms underlying EMT tristability |
title | Distinguishing mechanisms underlying EMT tristability |
title_full | Distinguishing mechanisms underlying EMT tristability |
title_fullStr | Distinguishing mechanisms underlying EMT tristability |
title_full_unstemmed | Distinguishing mechanisms underlying EMT tristability |
title_short | Distinguishing mechanisms underlying EMT tristability |
title_sort | distinguishing mechanisms underlying emt tristability |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5876698/ https://www.ncbi.nlm.nih.gov/pubmed/29623961 http://dx.doi.org/10.1186/s41236-017-0005-8 |
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