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Reciprocal regulatory circuits coordinating EMT plasticity

Epithelial to mesenchymal transition (EMT) as well as its reversal process, mesenchymal to epithelial transition (MET), are essential and well-controlled cellular processes during embryonic development. Tightly controlled regulatory mechanisms guide an EMT/MET plasticity and enable cells to switch f...

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Detalles Bibliográficos
Autores principales: Diepenbruck, Maren, Christofori, Gerhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shared Science Publishers OG 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6551634/
https://www.ncbi.nlm.nih.gov/pubmed/31225444
http://dx.doi.org/10.15698/cst2017.12.117
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author Diepenbruck, Maren
Christofori, Gerhard
author_facet Diepenbruck, Maren
Christofori, Gerhard
author_sort Diepenbruck, Maren
collection PubMed
description Epithelial to mesenchymal transition (EMT) as well as its reversal process, mesenchymal to epithelial transition (MET), are essential and well-controlled cellular processes during embryonic development. Tightly controlled regulatory mechanisms guide an EMT/MET plasticity and enable cells to switch forth and back between different cell morphologies and functional capabilities to endow the necessity of tissue plasticity. However, aberrant and uncontrolled activation of these processes during malignant tumor progression promotes primary tumor cell invasion, cancer cell dissemination and metastatic outgrowth. In a recent study (Nat Commun; doi: 10.1038/s41467-017-01197-w), we have reported on the post-transcriptional control of normal and cancer-associated EMT by miRNAs and identified a novel, critical double-negative feedback regulation of the thus far unknown miRNA miR1199 and the key EMT transcription factor Zeb1.
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spelling pubmed-65516342019-06-20 Reciprocal regulatory circuits coordinating EMT plasticity Diepenbruck, Maren Christofori, Gerhard Cell Stress Microreview Epithelial to mesenchymal transition (EMT) as well as its reversal process, mesenchymal to epithelial transition (MET), are essential and well-controlled cellular processes during embryonic development. Tightly controlled regulatory mechanisms guide an EMT/MET plasticity and enable cells to switch forth and back between different cell morphologies and functional capabilities to endow the necessity of tissue plasticity. However, aberrant and uncontrolled activation of these processes during malignant tumor progression promotes primary tumor cell invasion, cancer cell dissemination and metastatic outgrowth. In a recent study (Nat Commun; doi: 10.1038/s41467-017-01197-w), we have reported on the post-transcriptional control of normal and cancer-associated EMT by miRNAs and identified a novel, critical double-negative feedback regulation of the thus far unknown miRNA miR1199 and the key EMT transcription factor Zeb1. Shared Science Publishers OG 2017-12-01 /pmc/articles/PMC6551634/ /pubmed/31225444 http://dx.doi.org/10.15698/cst2017.12.117 Text en Copyright: © 2017 Diepenbruck and Christofori https://creativecommons.org/licenses/by/4.0/ This is an open-access article released under the terms of the Creative Commons Attribution (CC BY) license, which allows the unrestricted use, distribution, and reproduction in any medium, provided the original author and source are acknowledged.
spellingShingle Microreview
Diepenbruck, Maren
Christofori, Gerhard
Reciprocal regulatory circuits coordinating EMT plasticity
title Reciprocal regulatory circuits coordinating EMT plasticity
title_full Reciprocal regulatory circuits coordinating EMT plasticity
title_fullStr Reciprocal regulatory circuits coordinating EMT plasticity
title_full_unstemmed Reciprocal regulatory circuits coordinating EMT plasticity
title_short Reciprocal regulatory circuits coordinating EMT plasticity
title_sort reciprocal regulatory circuits coordinating emt plasticity
topic Microreview
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6551634/
https://www.ncbi.nlm.nih.gov/pubmed/31225444
http://dx.doi.org/10.15698/cst2017.12.117
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