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High level of HSF1 associates with aggressive endometrial carcinoma and suggests potential for HSP90 inhibitors
BACKGROUND: Recent identification of a specific role of HSF1 in cancer progression has led to new relevance of HSF1 as both a prognostic and a predictive marker. The role of HSF1 in endometrial cancer has so far been unexplored. METHODS: A total of 823 lesions from endometrial carcinoma precursors,...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4090731/ https://www.ncbi.nlm.nih.gov/pubmed/24853175 http://dx.doi.org/10.1038/bjc.2014.262 |
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author | Engerud, H Tangen, I L Berg, A Kusonmano, K Halle, M K Øyan, A M Kalland, K H Stefansson, I Trovik, J Salvesen, H B Krakstad, C |
author_facet | Engerud, H Tangen, I L Berg, A Kusonmano, K Halle, M K Øyan, A M Kalland, K H Stefansson, I Trovik, J Salvesen, H B Krakstad, C |
author_sort | Engerud, H |
collection | PubMed |
description | BACKGROUND: Recent identification of a specific role of HSF1 in cancer progression has led to new relevance of HSF1 as both a prognostic and a predictive marker. The role of HSF1 in endometrial cancer has so far been unexplored. METHODS: A total of 823 lesions from endometrial carcinoma precursors, primary tumours and metastases were prospectively collected and explored for HSF1 protein expression in relation to established markers for aggressive disease and survival. Transcriptional alterations related to HSF1 protein level were investigated by microarray analysis for 224 freshly frozen samples in parallel. RESULTS: High expression of HSF1 protein in endometrial carcinoma is significantly associated with aggressive disease and poor survival (all P-values ⩽0.02), also among ERα-positive patients presumed to have good prognosis. The HSF1-related gene signatures increase during disease progression and were also found to have prognostic value. Gene expression analyses identified HSP90 inhibition as a potential novel therapeutic approach for cases with high protein expression of HSF1. CONCLUSIONS: We demonstrate for the first time in endometrial cancer that high expression of HSF1 and measures for transcriptional activation of HSF1 associate with poor outcome and disease progression. The HSP90 inhibitors are suggested as new targeted therapeutics for patients with high HSF1 levels in tumour in particular. |
format | Online Article Text |
id | pubmed-4090731 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-40907312015-07-01 High level of HSF1 associates with aggressive endometrial carcinoma and suggests potential for HSP90 inhibitors Engerud, H Tangen, I L Berg, A Kusonmano, K Halle, M K Øyan, A M Kalland, K H Stefansson, I Trovik, J Salvesen, H B Krakstad, C Br J Cancer Translational Therapeutics BACKGROUND: Recent identification of a specific role of HSF1 in cancer progression has led to new relevance of HSF1 as both a prognostic and a predictive marker. The role of HSF1 in endometrial cancer has so far been unexplored. METHODS: A total of 823 lesions from endometrial carcinoma precursors, primary tumours and metastases were prospectively collected and explored for HSF1 protein expression in relation to established markers for aggressive disease and survival. Transcriptional alterations related to HSF1 protein level were investigated by microarray analysis for 224 freshly frozen samples in parallel. RESULTS: High expression of HSF1 protein in endometrial carcinoma is significantly associated with aggressive disease and poor survival (all P-values ⩽0.02), also among ERα-positive patients presumed to have good prognosis. The HSF1-related gene signatures increase during disease progression and were also found to have prognostic value. Gene expression analyses identified HSP90 inhibition as a potential novel therapeutic approach for cases with high protein expression of HSF1. CONCLUSIONS: We demonstrate for the first time in endometrial cancer that high expression of HSF1 and measures for transcriptional activation of HSF1 associate with poor outcome and disease progression. The HSP90 inhibitors are suggested as new targeted therapeutics for patients with high HSF1 levels in tumour in particular. Nature Publishing Group 2014-07-01 2014-05-22 /pmc/articles/PMC4090731/ /pubmed/24853175 http://dx.doi.org/10.1038/bjc.2014.262 Text en Copyright © 2014 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/3.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/ |
spellingShingle | Translational Therapeutics Engerud, H Tangen, I L Berg, A Kusonmano, K Halle, M K Øyan, A M Kalland, K H Stefansson, I Trovik, J Salvesen, H B Krakstad, C High level of HSF1 associates with aggressive endometrial carcinoma and suggests potential for HSP90 inhibitors |
title | High level of HSF1 associates with aggressive endometrial carcinoma and suggests potential for HSP90 inhibitors |
title_full | High level of HSF1 associates with aggressive endometrial carcinoma and suggests potential for HSP90 inhibitors |
title_fullStr | High level of HSF1 associates with aggressive endometrial carcinoma and suggests potential for HSP90 inhibitors |
title_full_unstemmed | High level of HSF1 associates with aggressive endometrial carcinoma and suggests potential for HSP90 inhibitors |
title_short | High level of HSF1 associates with aggressive endometrial carcinoma and suggests potential for HSP90 inhibitors |
title_sort | high level of hsf1 associates with aggressive endometrial carcinoma and suggests potential for hsp90 inhibitors |
topic | Translational Therapeutics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4090731/ https://www.ncbi.nlm.nih.gov/pubmed/24853175 http://dx.doi.org/10.1038/bjc.2014.262 |
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