Cargando…

Immunohistochemical assay for neuron-specific enolase, synaptophysin, and RB-associated protein as a diagnostic aid in advanced retinoblastomas

PURPOSE: We evaluated the expression of the neural markers, neuron-specific enolase, and synaptophysin, as a tool to confirm the diagnosis of retinoblastoma (RB) in undifferentiated and advanced tumors. Additionally, we determined whether the extent of RB-associated protein (pRb) expression is helpf...

Descripción completa

Detalles Bibliográficos
Autores principales: López López, José Carlos, Fernández Alonso, Nieves, Cuevas Álvarez, Juan, García-Caballero, Tomás, Pastor Jimeno, José Carlos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6029607/
https://www.ncbi.nlm.nih.gov/pubmed/29988700
http://dx.doi.org/10.2147/OPTH.S141503
_version_ 1783336997501272064
author López López, José Carlos
Fernández Alonso, Nieves
Cuevas Álvarez, Juan
García-Caballero, Tomás
Pastor Jimeno, José Carlos
author_facet López López, José Carlos
Fernández Alonso, Nieves
Cuevas Álvarez, Juan
García-Caballero, Tomás
Pastor Jimeno, José Carlos
author_sort López López, José Carlos
collection PubMed
description PURPOSE: We evaluated the expression of the neural markers, neuron-specific enolase, and synaptophysin, as a tool to confirm the diagnosis of retinoblastoma (RB) in undifferentiated and advanced tumors. Additionally, we determined whether the extent of RB-associated protein (pRb) expression is helpful in assessing the prognosis in RB patients. METHODS: Conventional whole tissue section and tissue microarray immunohistochemistry for neuron-specific enolase, synaptophysin, and pRb were carried out in a series of 22 RBs. RESULTS: Neuron-specific enolase and synaptophysin were expressed in 75%–100% of the tumor cells, and the staining intensity was strong. Two RBs expressed pRb in 75%–100% of the tumor cells, also with strong staining intensity. Concordance between the immunohistochemical outcomes for whole tissue staining and tissue microarray staining was 76.2% for neuron-specific enolase, 85.7% for synaptophysin, and 80.0% for pRb. CONCLUSION: Neuron-specific enolase and synaptophysin have the potential to be useful markers for the diagnosis of RBs. Extensive and strong pRb staining is not associated with less aggressive tumor behavior according to the pathologic classification of RBs.
format Online
Article
Text
id pubmed-6029607
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Dove Medical Press
record_format MEDLINE/PubMed
spelling pubmed-60296072018-07-09 Immunohistochemical assay for neuron-specific enolase, synaptophysin, and RB-associated protein as a diagnostic aid in advanced retinoblastomas López López, José Carlos Fernández Alonso, Nieves Cuevas Álvarez, Juan García-Caballero, Tomás Pastor Jimeno, José Carlos Clin Ophthalmol Original Research PURPOSE: We evaluated the expression of the neural markers, neuron-specific enolase, and synaptophysin, as a tool to confirm the diagnosis of retinoblastoma (RB) in undifferentiated and advanced tumors. Additionally, we determined whether the extent of RB-associated protein (pRb) expression is helpful in assessing the prognosis in RB patients. METHODS: Conventional whole tissue section and tissue microarray immunohistochemistry for neuron-specific enolase, synaptophysin, and pRb were carried out in a series of 22 RBs. RESULTS: Neuron-specific enolase and synaptophysin were expressed in 75%–100% of the tumor cells, and the staining intensity was strong. Two RBs expressed pRb in 75%–100% of the tumor cells, also with strong staining intensity. Concordance between the immunohistochemical outcomes for whole tissue staining and tissue microarray staining was 76.2% for neuron-specific enolase, 85.7% for synaptophysin, and 80.0% for pRb. CONCLUSION: Neuron-specific enolase and synaptophysin have the potential to be useful markers for the diagnosis of RBs. Extensive and strong pRb staining is not associated with less aggressive tumor behavior according to the pathologic classification of RBs. Dove Medical Press 2018-06-28 /pmc/articles/PMC6029607/ /pubmed/29988700 http://dx.doi.org/10.2147/OPTH.S141503 Text en © 2018 López López et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
López López, José Carlos
Fernández Alonso, Nieves
Cuevas Álvarez, Juan
García-Caballero, Tomás
Pastor Jimeno, José Carlos
Immunohistochemical assay for neuron-specific enolase, synaptophysin, and RB-associated protein as a diagnostic aid in advanced retinoblastomas
title Immunohistochemical assay for neuron-specific enolase, synaptophysin, and RB-associated protein as a diagnostic aid in advanced retinoblastomas
title_full Immunohistochemical assay for neuron-specific enolase, synaptophysin, and RB-associated protein as a diagnostic aid in advanced retinoblastomas
title_fullStr Immunohistochemical assay for neuron-specific enolase, synaptophysin, and RB-associated protein as a diagnostic aid in advanced retinoblastomas
title_full_unstemmed Immunohistochemical assay for neuron-specific enolase, synaptophysin, and RB-associated protein as a diagnostic aid in advanced retinoblastomas
title_short Immunohistochemical assay for neuron-specific enolase, synaptophysin, and RB-associated protein as a diagnostic aid in advanced retinoblastomas
title_sort immunohistochemical assay for neuron-specific enolase, synaptophysin, and rb-associated protein as a diagnostic aid in advanced retinoblastomas
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6029607/
https://www.ncbi.nlm.nih.gov/pubmed/29988700
http://dx.doi.org/10.2147/OPTH.S141503
work_keys_str_mv AT lopezlopezjosecarlos immunohistochemicalassayforneuronspecificenolasesynaptophysinandrbassociatedproteinasadiagnosticaidinadvancedretinoblastomas
AT fernandezalonsonieves immunohistochemicalassayforneuronspecificenolasesynaptophysinandrbassociatedproteinasadiagnosticaidinadvancedretinoblastomas
AT cuevasalvarezjuan immunohistochemicalassayforneuronspecificenolasesynaptophysinandrbassociatedproteinasadiagnosticaidinadvancedretinoblastomas
AT garciacaballerotomas immunohistochemicalassayforneuronspecificenolasesynaptophysinandrbassociatedproteinasadiagnosticaidinadvancedretinoblastomas
AT pastorjimenojosecarlos immunohistochemicalassayforneuronspecificenolasesynaptophysinandrbassociatedproteinasadiagnosticaidinadvancedretinoblastomas