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NFATc4 Regulates Sox9 Gene Expression in Acinar Cell Plasticity and Pancreatic Cancer Initiation

Acinar transdifferentiation toward a duct-like phenotype constitutes the defining response of acinar cells to external stress signals and is considered to be the initial step in pancreatic carcinogenesis. Despite the requirement for oncogenic Kras in pancreatic cancer (PDAC) development, oncogenic K...

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Autores principales: Hessmann, Elisabeth, Zhang, Jin-San, Chen, Nai-Ming, Hasselluhn, Marie, Liou, Geou-Yarh, Storz, Peter, Ellenrieder, Volker, Billadeau, Daniel D., Koenig, Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4677249/
https://www.ncbi.nlm.nih.gov/pubmed/26697077
http://dx.doi.org/10.1155/2016/5272498
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author Hessmann, Elisabeth
Zhang, Jin-San
Chen, Nai-Ming
Hasselluhn, Marie
Liou, Geou-Yarh
Storz, Peter
Ellenrieder, Volker
Billadeau, Daniel D.
Koenig, Alexander
author_facet Hessmann, Elisabeth
Zhang, Jin-San
Chen, Nai-Ming
Hasselluhn, Marie
Liou, Geou-Yarh
Storz, Peter
Ellenrieder, Volker
Billadeau, Daniel D.
Koenig, Alexander
author_sort Hessmann, Elisabeth
collection PubMed
description Acinar transdifferentiation toward a duct-like phenotype constitutes the defining response of acinar cells to external stress signals and is considered to be the initial step in pancreatic carcinogenesis. Despite the requirement for oncogenic Kras in pancreatic cancer (PDAC) development, oncogenic Kras is not sufficient to drive pancreatic carcinogenesis beyond the level of premalignancy. Instead, secondary events, such as inflammation-induced signaling activation of the epidermal growth factor (EGFR) or induction of Sox9 expression, are required for tumor formation. Herein, we aimed to dissect the mechanism that links EGFR signaling to Sox9 gene expression during acinar-to-ductal metaplasia in pancreatic tissue adaptation and PDAC initiation. We show that the inflammatory transcription factor NFATc4 is highly induced and localizes in the nucleus in response to inflammation-induced EGFR signaling. Moreover, we demonstrate that NFATc4 drives acinar-to-ductal conversion and PDAC initiation through direct transcriptional induction of Sox9. Therefore, strategies designed to disrupt NFATc4 induction might be beneficial in the prevention or therapy of PDAC.
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spelling pubmed-46772492015-12-22 NFATc4 Regulates Sox9 Gene Expression in Acinar Cell Plasticity and Pancreatic Cancer Initiation Hessmann, Elisabeth Zhang, Jin-San Chen, Nai-Ming Hasselluhn, Marie Liou, Geou-Yarh Storz, Peter Ellenrieder, Volker Billadeau, Daniel D. Koenig, Alexander Stem Cells Int Research Article Acinar transdifferentiation toward a duct-like phenotype constitutes the defining response of acinar cells to external stress signals and is considered to be the initial step in pancreatic carcinogenesis. Despite the requirement for oncogenic Kras in pancreatic cancer (PDAC) development, oncogenic Kras is not sufficient to drive pancreatic carcinogenesis beyond the level of premalignancy. Instead, secondary events, such as inflammation-induced signaling activation of the epidermal growth factor (EGFR) or induction of Sox9 expression, are required for tumor formation. Herein, we aimed to dissect the mechanism that links EGFR signaling to Sox9 gene expression during acinar-to-ductal metaplasia in pancreatic tissue adaptation and PDAC initiation. We show that the inflammatory transcription factor NFATc4 is highly induced and localizes in the nucleus in response to inflammation-induced EGFR signaling. Moreover, we demonstrate that NFATc4 drives acinar-to-ductal conversion and PDAC initiation through direct transcriptional induction of Sox9. Therefore, strategies designed to disrupt NFATc4 induction might be beneficial in the prevention or therapy of PDAC. Hindawi Publishing Corporation 2016 2015-11-30 /pmc/articles/PMC4677249/ /pubmed/26697077 http://dx.doi.org/10.1155/2016/5272498 Text en Copyright © 2016 Elisabeth Hessmann et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Hessmann, Elisabeth
Zhang, Jin-San
Chen, Nai-Ming
Hasselluhn, Marie
Liou, Geou-Yarh
Storz, Peter
Ellenrieder, Volker
Billadeau, Daniel D.
Koenig, Alexander
NFATc4 Regulates Sox9 Gene Expression in Acinar Cell Plasticity and Pancreatic Cancer Initiation
title NFATc4 Regulates Sox9 Gene Expression in Acinar Cell Plasticity and Pancreatic Cancer Initiation
title_full NFATc4 Regulates Sox9 Gene Expression in Acinar Cell Plasticity and Pancreatic Cancer Initiation
title_fullStr NFATc4 Regulates Sox9 Gene Expression in Acinar Cell Plasticity and Pancreatic Cancer Initiation
title_full_unstemmed NFATc4 Regulates Sox9 Gene Expression in Acinar Cell Plasticity and Pancreatic Cancer Initiation
title_short NFATc4 Regulates Sox9 Gene Expression in Acinar Cell Plasticity and Pancreatic Cancer Initiation
title_sort nfatc4 regulates sox9 gene expression in acinar cell plasticity and pancreatic cancer initiation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4677249/
https://www.ncbi.nlm.nih.gov/pubmed/26697077
http://dx.doi.org/10.1155/2016/5272498
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