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CXCR4: A new player in vestibular schwannoma pathogenesis

BACKGROUND: CXCR4 is a chemokine receptor that recruits blood stem cells and increases tumor cell growth and invasiveness. We examined CXCR4 expression in vestibular schwannomas (VS) from patients with and without neurofibromatosis type 2 (NF2) and correlated the levels with the patients’ clinical c...

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Autores principales: Breun, Maria, Schwerdtfeger, Alexandra, Martellotta, Donato Daniel, Kessler, Almuth F., Perez, Jose M., Monoranu, Camelia M, Ernestus, Ralf-Ingo, Matthies, Cordula, Löhr, Mario, Hagemann, Carsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5839412/
https://www.ncbi.nlm.nih.gov/pubmed/29515781
http://dx.doi.org/10.18632/oncotarget.24119
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author Breun, Maria
Schwerdtfeger, Alexandra
Martellotta, Donato Daniel
Kessler, Almuth F.
Perez, Jose M.
Monoranu, Camelia M
Ernestus, Ralf-Ingo
Matthies, Cordula
Löhr, Mario
Hagemann, Carsten
author_facet Breun, Maria
Schwerdtfeger, Alexandra
Martellotta, Donato Daniel
Kessler, Almuth F.
Perez, Jose M.
Monoranu, Camelia M
Ernestus, Ralf-Ingo
Matthies, Cordula
Löhr, Mario
Hagemann, Carsten
author_sort Breun, Maria
collection PubMed
description BACKGROUND: CXCR4 is a chemokine receptor that recruits blood stem cells and increases tumor cell growth and invasiveness. We examined CXCR4 expression in vestibular schwannomas (VS) from patients with and without neurofibromatosis type 2 (NF2) and correlated the levels with the patients’ clinical characteristics. The aim was to determine whether CXCR4 can be used as a prognostic marker and as a target for systemic therapy. RESULTS: Overall, CXCR4 mRNA levels were 4.6-fold higher in VS versus control; the levels were 4.9-fold higher in NF2 patients and 4.2-fold higher in sporadic VS patients. IHC and WB showed heterogeneous protein expression, and CXCR4 was expressed mainly in S100-positive Schwann cells. There was no correlation between the CXCR4 protein levels and tumor extension. However, there was a trend towards correlation between higher expression levels and greater hearing loss. MATERIALS AND METHODS: CXCR4 mRNA and protein levels were determined in VS samples (n = 60); of these, 30 samples were from patients with NF2. Healthy nerves from autopsies served as controls. CXCR4 mRNA levels were measured by PCR, and protein levels were measured by immunohistochemistry (IHC) and Western blotting (WB). Tumor extension and hearing loss were categorized according to the Hannover Classification as clinical parameters. CONCLUSIONS: CXCR4 mRNA was overexpressed in VS relative to healthy vestibular nerves, and there was a trend towards higher CXCR4 expression levels being correlated with greater functional impairment. Thus, CXCR4 may be a prognostic marker of VS, and CXCR4 inhibition has potential as a systemic approach for the treatment of VS.
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spelling pubmed-58394122018-03-07 CXCR4: A new player in vestibular schwannoma pathogenesis Breun, Maria Schwerdtfeger, Alexandra Martellotta, Donato Daniel Kessler, Almuth F. Perez, Jose M. Monoranu, Camelia M Ernestus, Ralf-Ingo Matthies, Cordula Löhr, Mario Hagemann, Carsten Oncotarget Research Paper BACKGROUND: CXCR4 is a chemokine receptor that recruits blood stem cells and increases tumor cell growth and invasiveness. We examined CXCR4 expression in vestibular schwannomas (VS) from patients with and without neurofibromatosis type 2 (NF2) and correlated the levels with the patients’ clinical characteristics. The aim was to determine whether CXCR4 can be used as a prognostic marker and as a target for systemic therapy. RESULTS: Overall, CXCR4 mRNA levels were 4.6-fold higher in VS versus control; the levels were 4.9-fold higher in NF2 patients and 4.2-fold higher in sporadic VS patients. IHC and WB showed heterogeneous protein expression, and CXCR4 was expressed mainly in S100-positive Schwann cells. There was no correlation between the CXCR4 protein levels and tumor extension. However, there was a trend towards correlation between higher expression levels and greater hearing loss. MATERIALS AND METHODS: CXCR4 mRNA and protein levels were determined in VS samples (n = 60); of these, 30 samples were from patients with NF2. Healthy nerves from autopsies served as controls. CXCR4 mRNA levels were measured by PCR, and protein levels were measured by immunohistochemistry (IHC) and Western blotting (WB). Tumor extension and hearing loss were categorized according to the Hannover Classification as clinical parameters. CONCLUSIONS: CXCR4 mRNA was overexpressed in VS relative to healthy vestibular nerves, and there was a trend towards higher CXCR4 expression levels being correlated with greater functional impairment. Thus, CXCR4 may be a prognostic marker of VS, and CXCR4 inhibition has potential as a systemic approach for the treatment of VS. Impact Journals LLC 2018-01-10 /pmc/articles/PMC5839412/ /pubmed/29515781 http://dx.doi.org/10.18632/oncotarget.24119 Text en Copyright: © 2018 Breun et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Breun, Maria
Schwerdtfeger, Alexandra
Martellotta, Donato Daniel
Kessler, Almuth F.
Perez, Jose M.
Monoranu, Camelia M
Ernestus, Ralf-Ingo
Matthies, Cordula
Löhr, Mario
Hagemann, Carsten
CXCR4: A new player in vestibular schwannoma pathogenesis
title CXCR4: A new player in vestibular schwannoma pathogenesis
title_full CXCR4: A new player in vestibular schwannoma pathogenesis
title_fullStr CXCR4: A new player in vestibular schwannoma pathogenesis
title_full_unstemmed CXCR4: A new player in vestibular schwannoma pathogenesis
title_short CXCR4: A new player in vestibular schwannoma pathogenesis
title_sort cxcr4: a new player in vestibular schwannoma pathogenesis
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5839412/
https://www.ncbi.nlm.nih.gov/pubmed/29515781
http://dx.doi.org/10.18632/oncotarget.24119
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