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Reduced PTEN expression in the pancreas overexpressing transforming growth factor-beta 1

PTEN is a candidate tumour suppressor gene and frequently mutated in multiple cancers, however, not in pancreatic cancer. Recently, it has been demonstrated that PTEN expression is regulated by TGF-β1. Using TGF-β1 transgenic mice (n=7) and wildtype littermates (n=6), as well as pancreatic tissues o...

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Autores principales: Ebert, M P A, Fei, G, Schandl, L, Mawrin, C, Dietzmann, K, Herrera, P, Friess, H, Gress, T M, Malfertheiner, P
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2375189/
https://www.ncbi.nlm.nih.gov/pubmed/11870516
http://dx.doi.org/10.1038/sj.bjc.6600031
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author Ebert, M P A
Fei, G
Schandl, L
Mawrin, C
Dietzmann, K
Herrera, P
Friess, H
Gress, T M
Malfertheiner, P
author_facet Ebert, M P A
Fei, G
Schandl, L
Mawrin, C
Dietzmann, K
Herrera, P
Friess, H
Gress, T M
Malfertheiner, P
author_sort Ebert, M P A
collection PubMed
description PTEN is a candidate tumour suppressor gene and frequently mutated in multiple cancers, however, not in pancreatic cancer. Recently, it has been demonstrated that PTEN expression is regulated by TGF-β1. Using TGF-β1 transgenic mice (n=7) and wildtype littermates (n=6), as well as pancreatic tissues obtained from organ donors (n=10) and patients with pancreatic cancer (n=10), we assessed the expression of PTEN by means of immunohistochemistry and semiquantitative PCR analysis. In addition, PANC-1 cells were treated with TGF-β1 in vitro and the levels of PTEN mRNA were determined in these cells. In human pancreatic cancers PTEN mRNA levels were significantly decreased (P<0.05). In addition, in the pancreas of TGF-β1 transgenic mice the expression of PTEN was significantly reduced (P<0.01), as compared to wildtype littermates and incubation of PANC-1 cells with TGF-β1 decreased PTEN mRNA levels after 24 h. Inasmuch as TGF-β1 decreases PTEN expression in human pancreatic cancer cells and human pancreatic cancers overexpress TGF-β1, the reduced expression of PTEN in pancreatic cancer may be mediated by TGF-β1 overexpression. Thus, although PTEN is not mutated in pancreatic cancers, the reduction of its expression may give pancreatic cancer cells an additional growth advantage. British Journal of Cancer (2002) 86, 257–262. DOI: 10.1038/sj/bjc/6600031 www.bjcancer.com © 2002 The Cancer Research Campaign
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spelling pubmed-23751892009-09-10 Reduced PTEN expression in the pancreas overexpressing transforming growth factor-beta 1 Ebert, M P A Fei, G Schandl, L Mawrin, C Dietzmann, K Herrera, P Friess, H Gress, T M Malfertheiner, P Br J Cancer Molecular and Cellular Pathology PTEN is a candidate tumour suppressor gene and frequently mutated in multiple cancers, however, not in pancreatic cancer. Recently, it has been demonstrated that PTEN expression is regulated by TGF-β1. Using TGF-β1 transgenic mice (n=7) and wildtype littermates (n=6), as well as pancreatic tissues obtained from organ donors (n=10) and patients with pancreatic cancer (n=10), we assessed the expression of PTEN by means of immunohistochemistry and semiquantitative PCR analysis. In addition, PANC-1 cells were treated with TGF-β1 in vitro and the levels of PTEN mRNA were determined in these cells. In human pancreatic cancers PTEN mRNA levels were significantly decreased (P<0.05). In addition, in the pancreas of TGF-β1 transgenic mice the expression of PTEN was significantly reduced (P<0.01), as compared to wildtype littermates and incubation of PANC-1 cells with TGF-β1 decreased PTEN mRNA levels after 24 h. Inasmuch as TGF-β1 decreases PTEN expression in human pancreatic cancer cells and human pancreatic cancers overexpress TGF-β1, the reduced expression of PTEN in pancreatic cancer may be mediated by TGF-β1 overexpression. Thus, although PTEN is not mutated in pancreatic cancers, the reduction of its expression may give pancreatic cancer cells an additional growth advantage. British Journal of Cancer (2002) 86, 257–262. DOI: 10.1038/sj/bjc/6600031 www.bjcancer.com © 2002 The Cancer Research Campaign Nature Publishing Group 2002-01-21 /pmc/articles/PMC2375189/ /pubmed/11870516 http://dx.doi.org/10.1038/sj.bjc.6600031 Text en Copyright © 2002 The Cancer Research Campaign 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 and Cellular Pathology
Ebert, M P A
Fei, G
Schandl, L
Mawrin, C
Dietzmann, K
Herrera, P
Friess, H
Gress, T M
Malfertheiner, P
Reduced PTEN expression in the pancreas overexpressing transforming growth factor-beta 1
title Reduced PTEN expression in the pancreas overexpressing transforming growth factor-beta 1
title_full Reduced PTEN expression in the pancreas overexpressing transforming growth factor-beta 1
title_fullStr Reduced PTEN expression in the pancreas overexpressing transforming growth factor-beta 1
title_full_unstemmed Reduced PTEN expression in the pancreas overexpressing transforming growth factor-beta 1
title_short Reduced PTEN expression in the pancreas overexpressing transforming growth factor-beta 1
title_sort reduced pten expression in the pancreas overexpressing transforming growth factor-beta 1
topic Molecular and Cellular Pathology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2375189/
https://www.ncbi.nlm.nih.gov/pubmed/11870516
http://dx.doi.org/10.1038/sj.bjc.6600031
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