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FOXA1 Gene Expression for Defining Molecular Subtypes of Muscle-Invasive Bladder Cancer after Radical Cystectomy
It remains unclear how to implement the recently revealed basal and luminal subtypes of muscle-invasive bladder cancer (MIBC) into daily clinical routine and whether molecular marker panels can be reduced. The mRNA expression of basal (KRT5) and luminal (FOXA1, GATA3, KRT20) markers was measured by...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7230662/ https://www.ncbi.nlm.nih.gov/pubmed/32252315 http://dx.doi.org/10.3390/jcm9040994 |
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author | Sikic, Danijel Eckstein, Markus Wirtz, Ralph M. Jarczyk, Jonas Worst, Thomas S. Porubsky, Stefan Keck, Bastian Kunath, Frank Weyerer, Veronika Breyer, Johannes Otto, Wolfgang Rinaldetti, Sebastien Bolenz, Christian Hartmann, Arndt Wullich, Bernd Erben, Philipp |
author_facet | Sikic, Danijel Eckstein, Markus Wirtz, Ralph M. Jarczyk, Jonas Worst, Thomas S. Porubsky, Stefan Keck, Bastian Kunath, Frank Weyerer, Veronika Breyer, Johannes Otto, Wolfgang Rinaldetti, Sebastien Bolenz, Christian Hartmann, Arndt Wullich, Bernd Erben, Philipp |
author_sort | Sikic, Danijel |
collection | PubMed |
description | It remains unclear how to implement the recently revealed basal and luminal subtypes of muscle-invasive bladder cancer (MIBC) into daily clinical routine and whether molecular marker panels can be reduced. The mRNA expression of basal (KRT5) and luminal (FOXA1, GATA3, KRT20) markers was measured by reverse transcription quantitative real-time polymerase chain reaction (RT-qPCR) and correlated to clinicopathological features, recurrence-free survival (RFS), disease-free survival (DFS), and overall survival (OS) in 80 patients with MIBC who underwent radical cystectomy. Additionally, the correlation of single markers with the basal and non-basal subtypes defined by a 36-gene panel was examined and then validated in the TCGA (The Cancer Genome Atlas) cohort. High expression of FOXA1 (p = 0.0048) and KRT20 (p = 0.0317) was associated with reduced RFS. In the multivariable analysis, only FOXA1 remained an independent prognostic marker for DFS (p = 0.0333) and RFS (p = 0.0310). FOXA1 expression (AUC = 0.79; p = 0.0007) was closest to the combined marker expression (AUC = 0.79; p = 0.0015) in resembling the non-basal subtype defined by the 36-gene panel. FOXA1 in combination with KRT5 may be used to distinguish the basal and non-basal subtypes of MIBC. |
format | Online Article Text |
id | pubmed-7230662 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-72306622020-05-22 FOXA1 Gene Expression for Defining Molecular Subtypes of Muscle-Invasive Bladder Cancer after Radical Cystectomy Sikic, Danijel Eckstein, Markus Wirtz, Ralph M. Jarczyk, Jonas Worst, Thomas S. Porubsky, Stefan Keck, Bastian Kunath, Frank Weyerer, Veronika Breyer, Johannes Otto, Wolfgang Rinaldetti, Sebastien Bolenz, Christian Hartmann, Arndt Wullich, Bernd Erben, Philipp J Clin Med Article It remains unclear how to implement the recently revealed basal and luminal subtypes of muscle-invasive bladder cancer (MIBC) into daily clinical routine and whether molecular marker panels can be reduced. The mRNA expression of basal (KRT5) and luminal (FOXA1, GATA3, KRT20) markers was measured by reverse transcription quantitative real-time polymerase chain reaction (RT-qPCR) and correlated to clinicopathological features, recurrence-free survival (RFS), disease-free survival (DFS), and overall survival (OS) in 80 patients with MIBC who underwent radical cystectomy. Additionally, the correlation of single markers with the basal and non-basal subtypes defined by a 36-gene panel was examined and then validated in the TCGA (The Cancer Genome Atlas) cohort. High expression of FOXA1 (p = 0.0048) and KRT20 (p = 0.0317) was associated with reduced RFS. In the multivariable analysis, only FOXA1 remained an independent prognostic marker for DFS (p = 0.0333) and RFS (p = 0.0310). FOXA1 expression (AUC = 0.79; p = 0.0007) was closest to the combined marker expression (AUC = 0.79; p = 0.0015) in resembling the non-basal subtype defined by the 36-gene panel. FOXA1 in combination with KRT5 may be used to distinguish the basal and non-basal subtypes of MIBC. MDPI 2020-04-02 /pmc/articles/PMC7230662/ /pubmed/32252315 http://dx.doi.org/10.3390/jcm9040994 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Sikic, Danijel Eckstein, Markus Wirtz, Ralph M. Jarczyk, Jonas Worst, Thomas S. Porubsky, Stefan Keck, Bastian Kunath, Frank Weyerer, Veronika Breyer, Johannes Otto, Wolfgang Rinaldetti, Sebastien Bolenz, Christian Hartmann, Arndt Wullich, Bernd Erben, Philipp FOXA1 Gene Expression for Defining Molecular Subtypes of Muscle-Invasive Bladder Cancer after Radical Cystectomy |
title | FOXA1 Gene Expression for Defining Molecular Subtypes of Muscle-Invasive Bladder Cancer after Radical Cystectomy |
title_full | FOXA1 Gene Expression for Defining Molecular Subtypes of Muscle-Invasive Bladder Cancer after Radical Cystectomy |
title_fullStr | FOXA1 Gene Expression for Defining Molecular Subtypes of Muscle-Invasive Bladder Cancer after Radical Cystectomy |
title_full_unstemmed | FOXA1 Gene Expression for Defining Molecular Subtypes of Muscle-Invasive Bladder Cancer after Radical Cystectomy |
title_short | FOXA1 Gene Expression for Defining Molecular Subtypes of Muscle-Invasive Bladder Cancer after Radical Cystectomy |
title_sort | foxa1 gene expression for defining molecular subtypes of muscle-invasive bladder cancer after radical cystectomy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7230662/ https://www.ncbi.nlm.nih.gov/pubmed/32252315 http://dx.doi.org/10.3390/jcm9040994 |
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