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ZEB1 in Pancreatic Cancer

Pancreatic cancer is one of the most malignant human neoplasias. On the molecular level, epithelial-mesenchymal transition (EMT) has been demonstrated to contribute to the malignant phenotype of pancreatic cancer cells. ZEB1 is a transcriptional repressor that has been identified as an inducer of EM...

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Detalles Bibliográficos
Autores principales: Wellner, Ulrich, Brabletz, Thomas, Keck, Tobias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3837326/
https://www.ncbi.nlm.nih.gov/pubmed/24281177
http://dx.doi.org/10.3390/cancers2031617
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author Wellner, Ulrich
Brabletz, Thomas
Keck, Tobias
author_facet Wellner, Ulrich
Brabletz, Thomas
Keck, Tobias
author_sort Wellner, Ulrich
collection PubMed
description Pancreatic cancer is one of the most malignant human neoplasias. On the molecular level, epithelial-mesenchymal transition (EMT) has been demonstrated to contribute to the malignant phenotype of pancreatic cancer cells. ZEB1 is a transcriptional repressor that has been identified as an inducer of EMT. A negative feedback loop between ZEB1 and microRNA-200c has been shown to regulate this EMT induction in various models. With respect to pancreatic cancer, primary effects of EMT comprise increased local and distant tumor cell dissemination. Another recently described feature of the EMT is the acquisition of cancer stem cell traits. For pancreatic cancer cells, antagonism between ZEB1 and stemness-inhibiting micro-RNAs has been demonstrated to contribute to this process, providing experimental support for the migrating cancer stem cell (MCSC) hypothesis. ZEB1 has also been shown to be associated with drug resistance of pancreatic cancer cells. This article reviews the biological functions of ZEB1 with a focus on pancreatic cancer.
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spelling pubmed-38373262013-11-22 ZEB1 in Pancreatic Cancer Wellner, Ulrich Brabletz, Thomas Keck, Tobias Cancers (Basel) Review Pancreatic cancer is one of the most malignant human neoplasias. On the molecular level, epithelial-mesenchymal transition (EMT) has been demonstrated to contribute to the malignant phenotype of pancreatic cancer cells. ZEB1 is a transcriptional repressor that has been identified as an inducer of EMT. A negative feedback loop between ZEB1 and microRNA-200c has been shown to regulate this EMT induction in various models. With respect to pancreatic cancer, primary effects of EMT comprise increased local and distant tumor cell dissemination. Another recently described feature of the EMT is the acquisition of cancer stem cell traits. For pancreatic cancer cells, antagonism between ZEB1 and stemness-inhibiting micro-RNAs has been demonstrated to contribute to this process, providing experimental support for the migrating cancer stem cell (MCSC) hypothesis. ZEB1 has also been shown to be associated with drug resistance of pancreatic cancer cells. This article reviews the biological functions of ZEB1 with a focus on pancreatic cancer. MDPI 2010-08-18 /pmc/articles/PMC3837326/ /pubmed/24281177 http://dx.doi.org/10.3390/cancers2031617 Text en © 2010 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Wellner, Ulrich
Brabletz, Thomas
Keck, Tobias
ZEB1 in Pancreatic Cancer
title ZEB1 in Pancreatic Cancer
title_full ZEB1 in Pancreatic Cancer
title_fullStr ZEB1 in Pancreatic Cancer
title_full_unstemmed ZEB1 in Pancreatic Cancer
title_short ZEB1 in Pancreatic Cancer
title_sort zeb1 in pancreatic cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3837326/
https://www.ncbi.nlm.nih.gov/pubmed/24281177
http://dx.doi.org/10.3390/cancers2031617
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