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Role of DNA Methylation Profile in Diagnosing Astroblastoma: A Case Report and Literature Review
Astroblastoma is a rare tumor of the central nervous system (CNS) with uncertain clinical behavior. Recently, DNA methylation profiling has been shown to provide a highly robust and reproducible approach for the classification of all CNS tumors across different age groups. By using DNA methylation p...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6502896/ https://www.ncbi.nlm.nih.gov/pubmed/31114608 http://dx.doi.org/10.3389/fgene.2019.00391 |
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author | Petruzzellis, Giuseppe Alessi, Iside Colafati, Giovanna Stefania Diomedi-Camassei, Francesca Ciolfi, Andrea Pedace, Lucia Cacchione, Antonella Carai, Andrea Tartaglia, Marco Mastronuzzi, Angela Miele, Evelina |
author_facet | Petruzzellis, Giuseppe Alessi, Iside Colafati, Giovanna Stefania Diomedi-Camassei, Francesca Ciolfi, Andrea Pedace, Lucia Cacchione, Antonella Carai, Andrea Tartaglia, Marco Mastronuzzi, Angela Miele, Evelina |
author_sort | Petruzzellis, Giuseppe |
collection | PubMed |
description | Astroblastoma is a rare tumor of the central nervous system (CNS) with uncertain clinical behavior. Recently, DNA methylation profiling has been shown to provide a highly robust and reproducible approach for the classification of all CNS tumors across different age groups. By using DNA methylation profiling, a subset of CNS high-grade tumors with astroblastoma-like morphology characterized by the meningioma 1 gene (MN1) rearrangements, has been identified; they were termed “CNS high-grade neuroepithelial tumors with MN1 alteration” (CNS-HGNET-MN1). Here, we describe a case of CNS-HGNET-MN1 diagnosed by DNA methylation profiling, using Illumina Infinium HumanMethylationEPIC BeadChip (EPIC), that offers the opportunity to conduct a brief literature review. The patient presented with an episode of partial seizures involving the right hemisoma. A gross total resection was performed. No other treatment was proposed in light of the histological and molecular findings. After 21 months, the patient is disease-free in good clinical conditions. Also in view of this case, we recommend DNA-methylation profiling as an important tool for diagnosis and more effective patient stratification and management. |
format | Online Article Text |
id | pubmed-6502896 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65028962019-05-21 Role of DNA Methylation Profile in Diagnosing Astroblastoma: A Case Report and Literature Review Petruzzellis, Giuseppe Alessi, Iside Colafati, Giovanna Stefania Diomedi-Camassei, Francesca Ciolfi, Andrea Pedace, Lucia Cacchione, Antonella Carai, Andrea Tartaglia, Marco Mastronuzzi, Angela Miele, Evelina Front Genet Genetics Astroblastoma is a rare tumor of the central nervous system (CNS) with uncertain clinical behavior. Recently, DNA methylation profiling has been shown to provide a highly robust and reproducible approach for the classification of all CNS tumors across different age groups. By using DNA methylation profiling, a subset of CNS high-grade tumors with astroblastoma-like morphology characterized by the meningioma 1 gene (MN1) rearrangements, has been identified; they were termed “CNS high-grade neuroepithelial tumors with MN1 alteration” (CNS-HGNET-MN1). Here, we describe a case of CNS-HGNET-MN1 diagnosed by DNA methylation profiling, using Illumina Infinium HumanMethylationEPIC BeadChip (EPIC), that offers the opportunity to conduct a brief literature review. The patient presented with an episode of partial seizures involving the right hemisoma. A gross total resection was performed. No other treatment was proposed in light of the histological and molecular findings. After 21 months, the patient is disease-free in good clinical conditions. Also in view of this case, we recommend DNA-methylation profiling as an important tool for diagnosis and more effective patient stratification and management. Frontiers Media S.A. 2019-04-30 /pmc/articles/PMC6502896/ /pubmed/31114608 http://dx.doi.org/10.3389/fgene.2019.00391 Text en Copyright © 2019 Petruzzellis, Alessi, Colafati, Diomedi-Camassei, Ciolfi, Pedace, Cacchione, Carai, Tartaglia, Mastronuzzi and Miele. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Genetics Petruzzellis, Giuseppe Alessi, Iside Colafati, Giovanna Stefania Diomedi-Camassei, Francesca Ciolfi, Andrea Pedace, Lucia Cacchione, Antonella Carai, Andrea Tartaglia, Marco Mastronuzzi, Angela Miele, Evelina Role of DNA Methylation Profile in Diagnosing Astroblastoma: A Case Report and Literature Review |
title | Role of DNA Methylation Profile in Diagnosing Astroblastoma: A Case Report and Literature Review |
title_full | Role of DNA Methylation Profile in Diagnosing Astroblastoma: A Case Report and Literature Review |
title_fullStr | Role of DNA Methylation Profile in Diagnosing Astroblastoma: A Case Report and Literature Review |
title_full_unstemmed | Role of DNA Methylation Profile in Diagnosing Astroblastoma: A Case Report and Literature Review |
title_short | Role of DNA Methylation Profile in Diagnosing Astroblastoma: A Case Report and Literature Review |
title_sort | role of dna methylation profile in diagnosing astroblastoma: a case report and literature review |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6502896/ https://www.ncbi.nlm.nih.gov/pubmed/31114608 http://dx.doi.org/10.3389/fgene.2019.00391 |
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