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Aurora kinase A (AURKA) expression in colorectal cancer liver metastasis is associated with poor prognosis

BACKGROUND: Five-year survival after resection of colorectal cancer liver metastasis (CRLCM) is <30%. We recently found that aurora kinase A (AURKA) drives 20q gain-associated tumour progression and is associated with disease recurrence. This study evaluates the prognostic value of AURKA expressi...

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Autores principales: Goos, J A C M, Coupe, V M H, Diosdado, B, Delis-Van Diemen, P M, Karga, C, Beliën, J A M, Carvalho, B, van den Tol, M P, Verheul, H M W, Geldof, A A, Meijer, G A, Hoekstra, O S, Fijneman, R J A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3817339/
https://www.ncbi.nlm.nih.gov/pubmed/24104968
http://dx.doi.org/10.1038/bjc.2013.608
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author Goos, J A C M
Coupe, V M H
Diosdado, B
Delis-Van Diemen, P M
Karga, C
Beliën, J A M
Carvalho, B
van den Tol, M P
Verheul, H M W
Geldof, A A
Meijer, G A
Hoekstra, O S
Fijneman, R J A
author_facet Goos, J A C M
Coupe, V M H
Diosdado, B
Delis-Van Diemen, P M
Karga, C
Beliën, J A M
Carvalho, B
van den Tol, M P
Verheul, H M W
Geldof, A A
Meijer, G A
Hoekstra, O S
Fijneman, R J A
author_sort Goos, J A C M
collection PubMed
description BACKGROUND: Five-year survival after resection of colorectal cancer liver metastasis (CRLCM) is <30%. We recently found that aurora kinase A (AURKA) drives 20q gain-associated tumour progression and is associated with disease recurrence. This study evaluates the prognostic value of AURKA expression in CRCLM of patients who underwent liver resection. METHODS: Tissue microarrays (TMAs) were generated using formalin-fixed paraffin-embedded CRCLM and matched primary tumour from a multi-institutional cohort of patients with CRCLM who underwent liver resection between 1990 and 2010. Tissue microarrays were stained for AURKA using immunohistochemistry, and a hazard rate ratio (HRR) for the association between overall survival (OS) and nuclear AURKA expression in CRCLM was calculated. Results were validated by 500-fold cross-validation. RESULTS: The expression of AURKA was evaluated in CRCLM of 343 patients. High AURKA expression was associated with poor OS (HRR 1.55, P<0.01), with a cross-validated average HRR of 1.57 (P=0.02). Average HRR was adjusted for the established prognostic clinicopathological variables in a multivariate analysis (average HRR 1.66; P=0.02). The expression of AURKA in CRCLM was correlated to its expression in corresponding primary tumour (P<0.01). CONCLUSION: The expression of AURKA protein is a molecular biomarker with prognostic value for patients with CRCLM, independent of established clinicopathological variables.
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spelling pubmed-38173392014-10-29 Aurora kinase A (AURKA) expression in colorectal cancer liver metastasis is associated with poor prognosis Goos, J A C M Coupe, V M H Diosdado, B Delis-Van Diemen, P M Karga, C Beliën, J A M Carvalho, B van den Tol, M P Verheul, H M W Geldof, A A Meijer, G A Hoekstra, O S Fijneman, R J A Br J Cancer Molecular Diagnostics BACKGROUND: Five-year survival after resection of colorectal cancer liver metastasis (CRLCM) is <30%. We recently found that aurora kinase A (AURKA) drives 20q gain-associated tumour progression and is associated with disease recurrence. This study evaluates the prognostic value of AURKA expression in CRCLM of patients who underwent liver resection. METHODS: Tissue microarrays (TMAs) were generated using formalin-fixed paraffin-embedded CRCLM and matched primary tumour from a multi-institutional cohort of patients with CRCLM who underwent liver resection between 1990 and 2010. Tissue microarrays were stained for AURKA using immunohistochemistry, and a hazard rate ratio (HRR) for the association between overall survival (OS) and nuclear AURKA expression in CRCLM was calculated. Results were validated by 500-fold cross-validation. RESULTS: The expression of AURKA was evaluated in CRCLM of 343 patients. High AURKA expression was associated with poor OS (HRR 1.55, P<0.01), with a cross-validated average HRR of 1.57 (P=0.02). Average HRR was adjusted for the established prognostic clinicopathological variables in a multivariate analysis (average HRR 1.66; P=0.02). The expression of AURKA in CRCLM was correlated to its expression in corresponding primary tumour (P<0.01). CONCLUSION: The expression of AURKA protein is a molecular biomarker with prognostic value for patients with CRCLM, independent of established clinicopathological variables. Nature Publishing Group 2013-10-29 2013-10-08 /pmc/articles/PMC3817339/ /pubmed/24104968 http://dx.doi.org/10.1038/bjc.2013.608 Text en Copyright © 2013 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
Goos, J A C M
Coupe, V M H
Diosdado, B
Delis-Van Diemen, P M
Karga, C
Beliën, J A M
Carvalho, B
van den Tol, M P
Verheul, H M W
Geldof, A A
Meijer, G A
Hoekstra, O S
Fijneman, R J A
Aurora kinase A (AURKA) expression in colorectal cancer liver metastasis is associated with poor prognosis
title Aurora kinase A (AURKA) expression in colorectal cancer liver metastasis is associated with poor prognosis
title_full Aurora kinase A (AURKA) expression in colorectal cancer liver metastasis is associated with poor prognosis
title_fullStr Aurora kinase A (AURKA) expression in colorectal cancer liver metastasis is associated with poor prognosis
title_full_unstemmed Aurora kinase A (AURKA) expression in colorectal cancer liver metastasis is associated with poor prognosis
title_short Aurora kinase A (AURKA) expression in colorectal cancer liver metastasis is associated with poor prognosis
title_sort aurora kinase a (aurka) expression in colorectal cancer liver metastasis is associated with poor prognosis
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3817339/
https://www.ncbi.nlm.nih.gov/pubmed/24104968
http://dx.doi.org/10.1038/bjc.2013.608
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