Cargando…

Fibroblast growth factor receptor 1 amplification in laryngeal squamous cell carcinoma

Fibroblast growth factor receptor 1 (FGFR1) has been noted to be amplified in a variety of squamous cell carcinomas (SCCa) of the head, neck, and lung and increased copy number (CN) is a predictor of poor outcomes. FGFR1 is a therapeutic target for lung SCCa and inhibition therapy is currently in cl...

Descripción completa

Detalles Bibliográficos
Autores principales: Monico, Jesus, Miller, Brandon, Rezeanu, Luminita, May, Warren, Sullivan, Donna C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5774678/
https://www.ncbi.nlm.nih.gov/pubmed/29351293
http://dx.doi.org/10.1371/journal.pone.0186185
_version_ 1783293785138003968
author Monico, Jesus
Miller, Brandon
Rezeanu, Luminita
May, Warren
Sullivan, Donna C.
author_facet Monico, Jesus
Miller, Brandon
Rezeanu, Luminita
May, Warren
Sullivan, Donna C.
author_sort Monico, Jesus
collection PubMed
description Fibroblast growth factor receptor 1 (FGFR1) has been noted to be amplified in a variety of squamous cell carcinomas (SCCa) of the head, neck, and lung and increased copy number (CN) is a predictor of poor outcomes. FGFR1 is a therapeutic target for lung SCCa and inhibition therapy is currently in clinical trials. Absolute quantification of FGFR1 from formalin fixed paraffin embedded (FFPE) tissue of laryngeal SCCa was examined in this retrospective study. A droplet digital polymerase chain reaction (ddPCR) was used for absolute quantitation of the FGFR1 gene CN. Of the 74 samples analyzed, FGFR1 CN analysis revealed 54% of samples had CN greater than 2 copies/cell (1.8–2.2 copies/cell), and 38% had CN values greater than 3. The mean and standard deviation FGFR1 CN was 4.17 ± 1.46 CN for African American patients (n = 41) and 3.78 ±1.85 CN for Caucasian patients (n = 31). Further, 60.9% of specimens from African Americans demonstrated increased FGFR1 CN compared to 48.4% of Caucasians. Two SCCA samples from Native American demonstrated increased FGFR1 CN (4.19 and 3.01 CN). The level of FGFR1 amplification did not correlate with tumor stage, lymph node staging, or metastasis. In this population, the proportion of patient samples with an FGFR1 amplification was three times higher than in reported for SCCA of the head and neck. Further, increased FGFR1 CN was observed in two racial groups not previously reported: African Americans and Native Americans. However, FGFR1 amplification is not prognostic in laryngeal squamous cell carcinomas.
format Online
Article
Text
id pubmed-5774678
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-57746782018-01-26 Fibroblast growth factor receptor 1 amplification in laryngeal squamous cell carcinoma Monico, Jesus Miller, Brandon Rezeanu, Luminita May, Warren Sullivan, Donna C. PLoS One Research Article Fibroblast growth factor receptor 1 (FGFR1) has been noted to be amplified in a variety of squamous cell carcinomas (SCCa) of the head, neck, and lung and increased copy number (CN) is a predictor of poor outcomes. FGFR1 is a therapeutic target for lung SCCa and inhibition therapy is currently in clinical trials. Absolute quantification of FGFR1 from formalin fixed paraffin embedded (FFPE) tissue of laryngeal SCCa was examined in this retrospective study. A droplet digital polymerase chain reaction (ddPCR) was used for absolute quantitation of the FGFR1 gene CN. Of the 74 samples analyzed, FGFR1 CN analysis revealed 54% of samples had CN greater than 2 copies/cell (1.8–2.2 copies/cell), and 38% had CN values greater than 3. The mean and standard deviation FGFR1 CN was 4.17 ± 1.46 CN for African American patients (n = 41) and 3.78 ±1.85 CN for Caucasian patients (n = 31). Further, 60.9% of specimens from African Americans demonstrated increased FGFR1 CN compared to 48.4% of Caucasians. Two SCCA samples from Native American demonstrated increased FGFR1 CN (4.19 and 3.01 CN). The level of FGFR1 amplification did not correlate with tumor stage, lymph node staging, or metastasis. In this population, the proportion of patient samples with an FGFR1 amplification was three times higher than in reported for SCCA of the head and neck. Further, increased FGFR1 CN was observed in two racial groups not previously reported: African Americans and Native Americans. However, FGFR1 amplification is not prognostic in laryngeal squamous cell carcinomas. Public Library of Science 2018-01-19 /pmc/articles/PMC5774678/ /pubmed/29351293 http://dx.doi.org/10.1371/journal.pone.0186185 Text en © 2018 Monico et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Monico, Jesus
Miller, Brandon
Rezeanu, Luminita
May, Warren
Sullivan, Donna C.
Fibroblast growth factor receptor 1 amplification in laryngeal squamous cell carcinoma
title Fibroblast growth factor receptor 1 amplification in laryngeal squamous cell carcinoma
title_full Fibroblast growth factor receptor 1 amplification in laryngeal squamous cell carcinoma
title_fullStr Fibroblast growth factor receptor 1 amplification in laryngeal squamous cell carcinoma
title_full_unstemmed Fibroblast growth factor receptor 1 amplification in laryngeal squamous cell carcinoma
title_short Fibroblast growth factor receptor 1 amplification in laryngeal squamous cell carcinoma
title_sort fibroblast growth factor receptor 1 amplification in laryngeal squamous cell carcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5774678/
https://www.ncbi.nlm.nih.gov/pubmed/29351293
http://dx.doi.org/10.1371/journal.pone.0186185
work_keys_str_mv AT monicojesus fibroblastgrowthfactorreceptor1amplificationinlaryngealsquamouscellcarcinoma
AT millerbrandon fibroblastgrowthfactorreceptor1amplificationinlaryngealsquamouscellcarcinoma
AT rezeanuluminita fibroblastgrowthfactorreceptor1amplificationinlaryngealsquamouscellcarcinoma
AT maywarren fibroblastgrowthfactorreceptor1amplificationinlaryngealsquamouscellcarcinoma
AT sullivandonnac fibroblastgrowthfactorreceptor1amplificationinlaryngealsquamouscellcarcinoma