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Necrosis related HIF-1α expression predicts prognosis in patients with endometrioid endometrial carcinoma
BACKGROUND: Hypoxia inducible factor 1α (HIF-1α) plays an essential role in the adaptive response of cells to hypoxia and is associated with aggressive tumour behaviour. We have shown p27(kip1), which is generally reduced in endometrial cancer, to be re-expressed in hypoxic regions. This possibly co...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2909981/ https://www.ncbi.nlm.nih.gov/pubmed/20565904 http://dx.doi.org/10.1186/1471-2407-10-307 |
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author | Seeber, Laura MS Horrée, Nicole van der Groep, Petra van der Wall, Elsken Verheijen, René HM van Diest, Paul J |
author_facet | Seeber, Laura MS Horrée, Nicole van der Groep, Petra van der Wall, Elsken Verheijen, René HM van Diest, Paul J |
author_sort | Seeber, Laura MS |
collection | PubMed |
description | BACKGROUND: Hypoxia inducible factor 1α (HIF-1α) plays an essential role in the adaptive response of cells to hypoxia and is associated with aggressive tumour behaviour. We have shown p27(kip1), which is generally reduced in endometrial cancer, to be re-expressed in hypoxic regions. This possibly contributes to survival of cancer cells. The aim of this study was to evaluate the prognostic value of HIF-1α and p27(kip )expression in patients with endometrioid endometrial cancer. METHODS: Expression levels of HIF-1α, CAIX, Glut-1, and p27(kip1 )were analyzed by immunohistochemistry. Percentage of positive cells, staining pattern (perinecrotic, diffuse, or mixed) and presence of necrosis were noted. RESULTS: Necrosis was correlated with shortened disease free survival (DFS) (p = 0.008) and overall survival (OS) (p = 0.045). For DFS, perinecrotic HIF-1α expression was also prognostic (p = 0.044). Moreover, high p27(kip1 )expression was an additional prognostic factor for these patients with perinecrotic HIF-1α expression. In multivariate Cox regression, perinecrotic HIF-expression emerged as an independent prognostic factor. Perinecrotic HIF-1α expression was significantly associated with CAIX and Glut-1 expression, pointing towards functional HIF-1. CONCLUSIONS: In patients with endometrioid endometrial cancer, necrosis and necrosis-related expression of HIF-1α are important prognostic factors. More aggressive adjuvant treatment might be necessary to improve the outcome of patients with these characteristics. |
format | Text |
id | pubmed-2909981 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29099812010-07-27 Necrosis related HIF-1α expression predicts prognosis in patients with endometrioid endometrial carcinoma Seeber, Laura MS Horrée, Nicole van der Groep, Petra van der Wall, Elsken Verheijen, René HM van Diest, Paul J BMC Cancer Research Article BACKGROUND: Hypoxia inducible factor 1α (HIF-1α) plays an essential role in the adaptive response of cells to hypoxia and is associated with aggressive tumour behaviour. We have shown p27(kip1), which is generally reduced in endometrial cancer, to be re-expressed in hypoxic regions. This possibly contributes to survival of cancer cells. The aim of this study was to evaluate the prognostic value of HIF-1α and p27(kip )expression in patients with endometrioid endometrial cancer. METHODS: Expression levels of HIF-1α, CAIX, Glut-1, and p27(kip1 )were analyzed by immunohistochemistry. Percentage of positive cells, staining pattern (perinecrotic, diffuse, or mixed) and presence of necrosis were noted. RESULTS: Necrosis was correlated with shortened disease free survival (DFS) (p = 0.008) and overall survival (OS) (p = 0.045). For DFS, perinecrotic HIF-1α expression was also prognostic (p = 0.044). Moreover, high p27(kip1 )expression was an additional prognostic factor for these patients with perinecrotic HIF-1α expression. In multivariate Cox regression, perinecrotic HIF-expression emerged as an independent prognostic factor. Perinecrotic HIF-1α expression was significantly associated with CAIX and Glut-1 expression, pointing towards functional HIF-1. CONCLUSIONS: In patients with endometrioid endometrial cancer, necrosis and necrosis-related expression of HIF-1α are important prognostic factors. More aggressive adjuvant treatment might be necessary to improve the outcome of patients with these characteristics. BioMed Central 2010-06-19 /pmc/articles/PMC2909981/ /pubmed/20565904 http://dx.doi.org/10.1186/1471-2407-10-307 Text en Copyright ©2010 Seeber 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 cited. |
spellingShingle | Research Article Seeber, Laura MS Horrée, Nicole van der Groep, Petra van der Wall, Elsken Verheijen, René HM van Diest, Paul J Necrosis related HIF-1α expression predicts prognosis in patients with endometrioid endometrial carcinoma |
title | Necrosis related HIF-1α expression predicts prognosis in patients with endometrioid endometrial carcinoma |
title_full | Necrosis related HIF-1α expression predicts prognosis in patients with endometrioid endometrial carcinoma |
title_fullStr | Necrosis related HIF-1α expression predicts prognosis in patients with endometrioid endometrial carcinoma |
title_full_unstemmed | Necrosis related HIF-1α expression predicts prognosis in patients with endometrioid endometrial carcinoma |
title_short | Necrosis related HIF-1α expression predicts prognosis in patients with endometrioid endometrial carcinoma |
title_sort | necrosis related hif-1α expression predicts prognosis in patients with endometrioid endometrial carcinoma |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2909981/ https://www.ncbi.nlm.nih.gov/pubmed/20565904 http://dx.doi.org/10.1186/1471-2407-10-307 |
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