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Cellular differentiation determines the expression of the hypoxia-inducible protein NDRG1 in pancreatic cancer

N-myc downstream-regulated gene-1 (NDRG1) is a recently described hypoxia-inducible protein that is upregulated in various human cancers. Pancreatic ductal adenocarcinoma, called pancreatic cancer, is a highly aggressive cancer that is characterised by its avascular structure, which results in a sev...

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Autores principales: Angst, E, Sibold, S, Tiffon, C, Weimann, R, Gloor, B, Candinas, D, Stroka, D
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2360652/
https://www.ncbi.nlm.nih.gov/pubmed/16832411
http://dx.doi.org/10.1038/sj.bjc.6603256
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author Angst, E
Sibold, S
Tiffon, C
Weimann, R
Gloor, B
Candinas, D
Stroka, D
author_facet Angst, E
Sibold, S
Tiffon, C
Weimann, R
Gloor, B
Candinas, D
Stroka, D
author_sort Angst, E
collection PubMed
description N-myc downstream-regulated gene-1 (NDRG1) is a recently described hypoxia-inducible protein that is upregulated in various human cancers. Pancreatic ductal adenocarcinoma, called pancreatic cancer, is a highly aggressive cancer that is characterised by its avascular structure, which results in a severe hypoxic environment. In this study, we investigated whether NDRG1 is upregulated in these tumours, thus providing a novel marker for malignant cells in the pancreas. By immunohistochemistry, we observed that NDRG1 was highly expressed in well-differentiated cells of pancreatic cancer, whereas the poorly differentiated tumour cells were negative. In addition, hyperplastic islets and ducts of nonquiescent pancreatic tissue were positive. To further explore its selective expression in tumours, two well-established pancreatic cancer cell lines of unequal differentiation status were exposed to 2% oxygen. NDRG1 mRNA and protein were upregulated by hypoxia in the moderately differentiated Capan-1 cells; however, its levels remained unchanged in the poorly differentiated Panc-1 cell line. Taken together, our data suggest that NDRG1 will not serve as a reliable marker of tumour cells in the pancreas, but may serve as a marker of differentiation. Furthermore, we present the novel finding that cellular differentiation may be an important factor that determines the hypoxia-induced regulation of NDRG1.
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spelling pubmed-23606522009-09-10 Cellular differentiation determines the expression of the hypoxia-inducible protein NDRG1 in pancreatic cancer Angst, E Sibold, S Tiffon, C Weimann, R Gloor, B Candinas, D Stroka, D Br J Cancer Molecular Diagnostics N-myc downstream-regulated gene-1 (NDRG1) is a recently described hypoxia-inducible protein that is upregulated in various human cancers. Pancreatic ductal adenocarcinoma, called pancreatic cancer, is a highly aggressive cancer that is characterised by its avascular structure, which results in a severe hypoxic environment. In this study, we investigated whether NDRG1 is upregulated in these tumours, thus providing a novel marker for malignant cells in the pancreas. By immunohistochemistry, we observed that NDRG1 was highly expressed in well-differentiated cells of pancreatic cancer, whereas the poorly differentiated tumour cells were negative. In addition, hyperplastic islets and ducts of nonquiescent pancreatic tissue were positive. To further explore its selective expression in tumours, two well-established pancreatic cancer cell lines of unequal differentiation status were exposed to 2% oxygen. NDRG1 mRNA and protein were upregulated by hypoxia in the moderately differentiated Capan-1 cells; however, its levels remained unchanged in the poorly differentiated Panc-1 cell line. Taken together, our data suggest that NDRG1 will not serve as a reliable marker of tumour cells in the pancreas, but may serve as a marker of differentiation. Furthermore, we present the novel finding that cellular differentiation may be an important factor that determines the hypoxia-induced regulation of NDRG1. Nature Publishing Group 2006-08-07 2006-07-11 /pmc/articles/PMC2360652/ /pubmed/16832411 http://dx.doi.org/10.1038/sj.bjc.6603256 Text en Copyright © 2006 Cancer Research UK https://creativecommons.org/licenses/by/4.0/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 https://creativecommons.org/licenses/by/4.0/.
spellingShingle Molecular Diagnostics
Angst, E
Sibold, S
Tiffon, C
Weimann, R
Gloor, B
Candinas, D
Stroka, D
Cellular differentiation determines the expression of the hypoxia-inducible protein NDRG1 in pancreatic cancer
title Cellular differentiation determines the expression of the hypoxia-inducible protein NDRG1 in pancreatic cancer
title_full Cellular differentiation determines the expression of the hypoxia-inducible protein NDRG1 in pancreatic cancer
title_fullStr Cellular differentiation determines the expression of the hypoxia-inducible protein NDRG1 in pancreatic cancer
title_full_unstemmed Cellular differentiation determines the expression of the hypoxia-inducible protein NDRG1 in pancreatic cancer
title_short Cellular differentiation determines the expression of the hypoxia-inducible protein NDRG1 in pancreatic cancer
title_sort cellular differentiation determines the expression of the hypoxia-inducible protein ndrg1 in pancreatic cancer
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2360652/
https://www.ncbi.nlm.nih.gov/pubmed/16832411
http://dx.doi.org/10.1038/sj.bjc.6603256
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