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Expression of histone deacetylases 1, 2 and 3 in urothelial bladder cancer
BACKGROUND: Histone deacetylases (HDACs) are known to be associated with an overexpression in different types of cancer such as colon and prostate cancer. In this study we aimed to evaluate the protein expression of class I HDACs in urothelial carcinoma of the bladder. METHODS: A tissue microarray c...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3995609/ https://www.ncbi.nlm.nih.gov/pubmed/24624923 http://dx.doi.org/10.1186/1472-6890-14-10 |
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author | Poyet, Cédric Jentsch, Bastian Hermanns, Thomas Schweckendiek, Daniel Seifert, Hans-Helge Schmidtpeter, Martin Sulser, Tullio Moch, Holger Wild, Peter J Kristiansen, Glen |
author_facet | Poyet, Cédric Jentsch, Bastian Hermanns, Thomas Schweckendiek, Daniel Seifert, Hans-Helge Schmidtpeter, Martin Sulser, Tullio Moch, Holger Wild, Peter J Kristiansen, Glen |
author_sort | Poyet, Cédric |
collection | PubMed |
description | BACKGROUND: Histone deacetylases (HDACs) are known to be associated with an overexpression in different types of cancer such as colon and prostate cancer. In this study we aimed to evaluate the protein expression of class I HDACs in urothelial carcinoma of the bladder. METHODS: A tissue microarray containing 348 tissuesamples from 174 patients with a primary urothelial carcinoma of the bladder was immunohistochemically stained for HDAC 1, 2 and 3. Intensity of staining was evaluated and the association with clinico-pathological features and prognosis was assessed. RESULTS: High HDAC expression levels were found in 40 to 60% of all investigated urothelial carcinomas (HDAC-1: 40%, HDAC-2: 42%, HDAC-3: 59%). HDAC-1 and HDAC-2 were significantly associated with higher tumour grades. Although all three markers could not predict progression in univariate analyses, high HDAC-1 expression was associated with a trend toward poorer prognosis. Patients with high-grade tumours and high expression levels of HDAC-1 were more likely to progress compared to all other patients (p < 0.05). CONCLUSIONS: High-grade noninvasive papillary bladder tumours are associated with high expression levels of HDAC-1 and HDAC-2. High grade tumours in combination with high expression of HDAC-1 showed a worse prognosis than the other tumours. The high expression levels of HDACs observed particularly in high grade urothelial bladder cancer clearly warrant subsequent studies on the potential use of HDAC inhibitors as a novel therapeutic approach. |
format | Online Article Text |
id | pubmed-3995609 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-39956092014-04-23 Expression of histone deacetylases 1, 2 and 3 in urothelial bladder cancer Poyet, Cédric Jentsch, Bastian Hermanns, Thomas Schweckendiek, Daniel Seifert, Hans-Helge Schmidtpeter, Martin Sulser, Tullio Moch, Holger Wild, Peter J Kristiansen, Glen BMC Clin Pathol Research Article BACKGROUND: Histone deacetylases (HDACs) are known to be associated with an overexpression in different types of cancer such as colon and prostate cancer. In this study we aimed to evaluate the protein expression of class I HDACs in urothelial carcinoma of the bladder. METHODS: A tissue microarray containing 348 tissuesamples from 174 patients with a primary urothelial carcinoma of the bladder was immunohistochemically stained for HDAC 1, 2 and 3. Intensity of staining was evaluated and the association with clinico-pathological features and prognosis was assessed. RESULTS: High HDAC expression levels were found in 40 to 60% of all investigated urothelial carcinomas (HDAC-1: 40%, HDAC-2: 42%, HDAC-3: 59%). HDAC-1 and HDAC-2 were significantly associated with higher tumour grades. Although all three markers could not predict progression in univariate analyses, high HDAC-1 expression was associated with a trend toward poorer prognosis. Patients with high-grade tumours and high expression levels of HDAC-1 were more likely to progress compared to all other patients (p < 0.05). CONCLUSIONS: High-grade noninvasive papillary bladder tumours are associated with high expression levels of HDAC-1 and HDAC-2. High grade tumours in combination with high expression of HDAC-1 showed a worse prognosis than the other tumours. The high expression levels of HDACs observed particularly in high grade urothelial bladder cancer clearly warrant subsequent studies on the potential use of HDAC inhibitors as a novel therapeutic approach. BioMed Central 2014-03-13 /pmc/articles/PMC3995609/ /pubmed/24624923 http://dx.doi.org/10.1186/1472-6890-14-10 Text en Copyright © 2014 Poyet et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. |
spellingShingle | Research Article Poyet, Cédric Jentsch, Bastian Hermanns, Thomas Schweckendiek, Daniel Seifert, Hans-Helge Schmidtpeter, Martin Sulser, Tullio Moch, Holger Wild, Peter J Kristiansen, Glen Expression of histone deacetylases 1, 2 and 3 in urothelial bladder cancer |
title | Expression of histone deacetylases 1, 2 and 3 in urothelial bladder cancer |
title_full | Expression of histone deacetylases 1, 2 and 3 in urothelial bladder cancer |
title_fullStr | Expression of histone deacetylases 1, 2 and 3 in urothelial bladder cancer |
title_full_unstemmed | Expression of histone deacetylases 1, 2 and 3 in urothelial bladder cancer |
title_short | Expression of histone deacetylases 1, 2 and 3 in urothelial bladder cancer |
title_sort | expression of histone deacetylases 1, 2 and 3 in urothelial bladder cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3995609/ https://www.ncbi.nlm.nih.gov/pubmed/24624923 http://dx.doi.org/10.1186/1472-6890-14-10 |
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