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Clinical prognostic value of combined analysis of Aldh1, Survivin, and EpCAM expression in colorectal cancer

BACKGROUND: Tumour aggressiveness might be related to the degree of main cancer hallmark acquirement of tumour cells, reflected by expression levels of specific biomarkers. We investigated the expression of Aldh1, Survivin, and EpCAM, together reflecting main cancer hallmarks, in relation to clinica...

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Autores principales: Goossens-Beumer, I J, Zeestraten, E C M, Benard, A, Christen, T, Reimers, M S, Keijzer, R, Sier, C F M, Liefers, G J, Morreau, H, Putter, H, Vahrmeijer, A L, van de Velde, C J H, Kuppen, P J K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4056050/
https://www.ncbi.nlm.nih.gov/pubmed/24786601
http://dx.doi.org/10.1038/bjc.2014.226
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author Goossens-Beumer, I J
Zeestraten, E C M
Benard, A
Christen, T
Reimers, M S
Keijzer, R
Sier, C F M
Liefers, G J
Morreau, H
Putter, H
Vahrmeijer, A L
van de Velde, C J H
Kuppen, P J K
author_facet Goossens-Beumer, I J
Zeestraten, E C M
Benard, A
Christen, T
Reimers, M S
Keijzer, R
Sier, C F M
Liefers, G J
Morreau, H
Putter, H
Vahrmeijer, A L
van de Velde, C J H
Kuppen, P J K
author_sort Goossens-Beumer, I J
collection PubMed
description BACKGROUND: Tumour aggressiveness might be related to the degree of main cancer hallmark acquirement of tumour cells, reflected by expression levels of specific biomarkers. We investigated the expression of Aldh1, Survivin, and EpCAM, together reflecting main cancer hallmarks, in relation to clinical outcome of colorectal cancer (CRC) patients. METHODS: Immunohistochemistry was performed using a tumour tissue microarray of TNM (Tumour, Node, Metastasis)-stage I–IV CRC tissues. Single-marker expression or their combination was assessed for associations with the clinical outcome of CRC patients (N=309). RESULTS: Increased expression of Aldh1 or Survivin, or decreased expression of EpCAM was each associated with poor clinical outcome, and was therefore identified as clinically unfavourable expression. Analyses of the combination of all three markers showed worse clinical outcome, specifically in colon cancer patients, with an increasing number of markers showing unfavourable expression. Hazard ratios ranged up to 8.3 for overall survival (P<0.001), 36.6 for disease-specific survival (P<0.001), and 27.1 for distant recurrence-free survival (P<0.001). CONCLUSIONS: Our data identified combined expression levels of Aldh1, Survivin, and EpCAM as strong independent prognostic factors, with high hazard ratios, for survival and tumour recurrence in colon cancer patients, and therefore reflect tumour aggressiveness.
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spelling pubmed-40560502015-06-10 Clinical prognostic value of combined analysis of Aldh1, Survivin, and EpCAM expression in colorectal cancer Goossens-Beumer, I J Zeestraten, E C M Benard, A Christen, T Reimers, M S Keijzer, R Sier, C F M Liefers, G J Morreau, H Putter, H Vahrmeijer, A L van de Velde, C J H Kuppen, P J K Br J Cancer Molecular Diagnostics BACKGROUND: Tumour aggressiveness might be related to the degree of main cancer hallmark acquirement of tumour cells, reflected by expression levels of specific biomarkers. We investigated the expression of Aldh1, Survivin, and EpCAM, together reflecting main cancer hallmarks, in relation to clinical outcome of colorectal cancer (CRC) patients. METHODS: Immunohistochemistry was performed using a tumour tissue microarray of TNM (Tumour, Node, Metastasis)-stage I–IV CRC tissues. Single-marker expression or their combination was assessed for associations with the clinical outcome of CRC patients (N=309). RESULTS: Increased expression of Aldh1 or Survivin, or decreased expression of EpCAM was each associated with poor clinical outcome, and was therefore identified as clinically unfavourable expression. Analyses of the combination of all three markers showed worse clinical outcome, specifically in colon cancer patients, with an increasing number of markers showing unfavourable expression. Hazard ratios ranged up to 8.3 for overall survival (P<0.001), 36.6 for disease-specific survival (P<0.001), and 27.1 for distant recurrence-free survival (P<0.001). CONCLUSIONS: Our data identified combined expression levels of Aldh1, Survivin, and EpCAM as strong independent prognostic factors, with high hazard ratios, for survival and tumour recurrence in colon cancer patients, and therefore reflect tumour aggressiveness. Nature Publishing Group 2014-06-10 2014-05-01 /pmc/articles/PMC4056050/ /pubmed/24786601 http://dx.doi.org/10.1038/bjc.2014.226 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 Molecular Diagnostics
Goossens-Beumer, I J
Zeestraten, E C M
Benard, A
Christen, T
Reimers, M S
Keijzer, R
Sier, C F M
Liefers, G J
Morreau, H
Putter, H
Vahrmeijer, A L
van de Velde, C J H
Kuppen, P J K
Clinical prognostic value of combined analysis of Aldh1, Survivin, and EpCAM expression in colorectal cancer
title Clinical prognostic value of combined analysis of Aldh1, Survivin, and EpCAM expression in colorectal cancer
title_full Clinical prognostic value of combined analysis of Aldh1, Survivin, and EpCAM expression in colorectal cancer
title_fullStr Clinical prognostic value of combined analysis of Aldh1, Survivin, and EpCAM expression in colorectal cancer
title_full_unstemmed Clinical prognostic value of combined analysis of Aldh1, Survivin, and EpCAM expression in colorectal cancer
title_short Clinical prognostic value of combined analysis of Aldh1, Survivin, and EpCAM expression in colorectal cancer
title_sort clinical prognostic value of combined analysis of aldh1, survivin, and epcam expression in colorectal cancer
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4056050/
https://www.ncbi.nlm.nih.gov/pubmed/24786601
http://dx.doi.org/10.1038/bjc.2014.226
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