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Chondroitin Sulphate Proteoglycan 4 (NG2/CSPG4) Localization in Low- and High-Grade Gliomas

Background: Neuron glial antigen 2 or chondroitin sulphate proteoglycan 4 (NG2/CSPG4) is expressed by immature precursors/progenitor cells and is possibly involved in malignant cell transformation. The aim of this study was to investigate its role on the progression and survival of sixty-one adult g...

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Autores principales: Mellai, Marta, Annovazzi, Laura, Bisogno, Ilaria, Corona, Cristiano, Crociara, Paola, Iulini, Barbara, Cassoni, Paola, Casalone, Cristina, Boldorini, Renzo, Schiffer, Davide
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7349878/
https://www.ncbi.nlm.nih.gov/pubmed/32599896
http://dx.doi.org/10.3390/cells9061538
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author Mellai, Marta
Annovazzi, Laura
Bisogno, Ilaria
Corona, Cristiano
Crociara, Paola
Iulini, Barbara
Cassoni, Paola
Casalone, Cristina
Boldorini, Renzo
Schiffer, Davide
author_facet Mellai, Marta
Annovazzi, Laura
Bisogno, Ilaria
Corona, Cristiano
Crociara, Paola
Iulini, Barbara
Cassoni, Paola
Casalone, Cristina
Boldorini, Renzo
Schiffer, Davide
author_sort Mellai, Marta
collection PubMed
description Background: Neuron glial antigen 2 or chondroitin sulphate proteoglycan 4 (NG2/CSPG4) is expressed by immature precursors/progenitor cells and is possibly involved in malignant cell transformation. The aim of this study was to investigate its role on the progression and survival of sixty-one adult gliomas and nine glioblastoma (GB)-derived cell lines. Methods: NG2/CSPG4 protein expression was assessed by immunohistochemistry and immunofluorescence. Genetic and epigenetic alterations were detected by molecular genetic techniques. Results: NG2/CSPG4 was frequently expressed in IDH-mutant/1p19q-codel oligodendrogliomas (59.1%) and IDH-wild type GBs (40%) and rarely expressed in IDH-mutant or IDH-wild type astrocytomas (14.3%). Besides tumor cells, NG2/CSPG4 immunoreactivity was found in the cytoplasm and/or cell membranes of reactive astrocytes and vascular pericytes/endothelial cells. In GB-derived neurospheres, it was variably detected according to the number of passages of the in vitro culture. In GB-derived adherent cells, a diffuse positivity was found in most cells. NG2/CSPG4 expression was significantly associated with EGFR gene amplification (p = 0.0005) and poor prognosis (p = 0.016) in astrocytic tumors. Conclusion: The immunoreactivity of NG2/CSPG4 provides information on the timing of the neoplastic transformation and could have prognostic and therapeutic relevance as a promising tumor-associated antigen for antibody-based immunotherapy in patients with malignant gliomas.
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spelling pubmed-73498782020-07-15 Chondroitin Sulphate Proteoglycan 4 (NG2/CSPG4) Localization in Low- and High-Grade Gliomas Mellai, Marta Annovazzi, Laura Bisogno, Ilaria Corona, Cristiano Crociara, Paola Iulini, Barbara Cassoni, Paola Casalone, Cristina Boldorini, Renzo Schiffer, Davide Cells Article Background: Neuron glial antigen 2 or chondroitin sulphate proteoglycan 4 (NG2/CSPG4) is expressed by immature precursors/progenitor cells and is possibly involved in malignant cell transformation. The aim of this study was to investigate its role on the progression and survival of sixty-one adult gliomas and nine glioblastoma (GB)-derived cell lines. Methods: NG2/CSPG4 protein expression was assessed by immunohistochemistry and immunofluorescence. Genetic and epigenetic alterations were detected by molecular genetic techniques. Results: NG2/CSPG4 was frequently expressed in IDH-mutant/1p19q-codel oligodendrogliomas (59.1%) and IDH-wild type GBs (40%) and rarely expressed in IDH-mutant or IDH-wild type astrocytomas (14.3%). Besides tumor cells, NG2/CSPG4 immunoreactivity was found in the cytoplasm and/or cell membranes of reactive astrocytes and vascular pericytes/endothelial cells. In GB-derived neurospheres, it was variably detected according to the number of passages of the in vitro culture. In GB-derived adherent cells, a diffuse positivity was found in most cells. NG2/CSPG4 expression was significantly associated with EGFR gene amplification (p = 0.0005) and poor prognosis (p = 0.016) in astrocytic tumors. Conclusion: The immunoreactivity of NG2/CSPG4 provides information on the timing of the neoplastic transformation and could have prognostic and therapeutic relevance as a promising tumor-associated antigen for antibody-based immunotherapy in patients with malignant gliomas. MDPI 2020-06-24 /pmc/articles/PMC7349878/ /pubmed/32599896 http://dx.doi.org/10.3390/cells9061538 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
Mellai, Marta
Annovazzi, Laura
Bisogno, Ilaria
Corona, Cristiano
Crociara, Paola
Iulini, Barbara
Cassoni, Paola
Casalone, Cristina
Boldorini, Renzo
Schiffer, Davide
Chondroitin Sulphate Proteoglycan 4 (NG2/CSPG4) Localization in Low- and High-Grade Gliomas
title Chondroitin Sulphate Proteoglycan 4 (NG2/CSPG4) Localization in Low- and High-Grade Gliomas
title_full Chondroitin Sulphate Proteoglycan 4 (NG2/CSPG4) Localization in Low- and High-Grade Gliomas
title_fullStr Chondroitin Sulphate Proteoglycan 4 (NG2/CSPG4) Localization in Low- and High-Grade Gliomas
title_full_unstemmed Chondroitin Sulphate Proteoglycan 4 (NG2/CSPG4) Localization in Low- and High-Grade Gliomas
title_short Chondroitin Sulphate Proteoglycan 4 (NG2/CSPG4) Localization in Low- and High-Grade Gliomas
title_sort chondroitin sulphate proteoglycan 4 (ng2/cspg4) localization in low- and high-grade gliomas
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7349878/
https://www.ncbi.nlm.nih.gov/pubmed/32599896
http://dx.doi.org/10.3390/cells9061538
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