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Diagnostics of pediatric supratentorial RELA ependymomas: integration of information from histopathology, genetics, DNA methylation and imaging
Ependymoma with RELA fusion has been defined as a novel entity of the revised World Health Organization 2016 classification of tumors of the central nervous system (CNS), characterized by fusion transcripts of the RELA gene and consequent pathological activation of the NFkB pathway. These tumors rep...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7379587/ https://www.ncbi.nlm.nih.gov/pubmed/30325077 http://dx.doi.org/10.1111/bpa.12664 |
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author | Pagès, Mélanie Pajtler, Kristian W. Puget, Stéphanie Castel, David Boddaert, Nathalie Tauziède‐Espariat, Arnault Picot, Stéphanie Debily, Marie‐Anne Kool, Marcel Capper, David Sainte‐Rose, Christian Chrétien, Fabrice Pfister, Stefan M. Pietsch, Torsten Grill, Jacques Varlet, Pascale Andreiuolo, Felipe |
author_facet | Pagès, Mélanie Pajtler, Kristian W. Puget, Stéphanie Castel, David Boddaert, Nathalie Tauziède‐Espariat, Arnault Picot, Stéphanie Debily, Marie‐Anne Kool, Marcel Capper, David Sainte‐Rose, Christian Chrétien, Fabrice Pfister, Stefan M. Pietsch, Torsten Grill, Jacques Varlet, Pascale Andreiuolo, Felipe |
author_sort | Pagès, Mélanie |
collection | PubMed |
description | Ependymoma with RELA fusion has been defined as a novel entity of the revised World Health Organization 2016 classification of tumors of the central nervous system (CNS), characterized by fusion transcripts of the RELA gene and consequent pathological activation of the NFkB pathway. These tumors represent the majority of supratentorial ependymomas in children. The validation of diagnostic tools to identify this clinically relevant ependymoma entity is essential. Here, we have used interphase fluorescent in situ hybridization (FISH) for C11orf95 and RELA, immunohistochemistry (IHC) for p65‐RelA and the recently developed DNA methylation‐based classification besides conventional histopathology, and compared the precision of the methods in 40 supratentorial pediatric brain tumors diagnosed as ependymomas in the past years. Reverse transcription PCR (RT‐PCR) and RNA sequencing were performed to explore discordant cases. Furthermore, we integrated imaging and clinical features as additional layers of information. The concordance between nuclear RelA expression by IHC and RELA FISH was 100%. Concordance between IHC and DNA methylation profiling, and between FISH and DNA methylation profiling was also high (96.4% and 95.2%, respectively). Thirty‐four out of 40 (85%) cases were confirmed by integrated diagnoses as ependymal tumors, including 22 RELA‐fused ependymomas (71% of ependymal tumors), two YAP1‐fused ependymomas (6%), six non‐RELA/non‐YAP1 ependymomas (18%) and four ependymal/subependymal mixed tumors (12%). Ependymal/subependymal mixed tumors had an excellent clinical outcome despite the presence of histopathological signs of malignancy, suggesting that these tumors should not be diagnosed as classic ependymomas. DNA methylation profiling helped in the differential diagnosis of RELA‐fused ependymomas. IHC and FISH, which are available in the majority of pathology laboratories, are valuable tools to identify RELA‐fused ependymomas. |
format | Online Article Text |
id | pubmed-7379587 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73795872020-07-24 Diagnostics of pediatric supratentorial RELA ependymomas: integration of information from histopathology, genetics, DNA methylation and imaging Pagès, Mélanie Pajtler, Kristian W. Puget, Stéphanie Castel, David Boddaert, Nathalie Tauziède‐Espariat, Arnault Picot, Stéphanie Debily, Marie‐Anne Kool, Marcel Capper, David Sainte‐Rose, Christian Chrétien, Fabrice Pfister, Stefan M. Pietsch, Torsten Grill, Jacques Varlet, Pascale Andreiuolo, Felipe Brain Pathol Research Articles Ependymoma with RELA fusion has been defined as a novel entity of the revised World Health Organization 2016 classification of tumors of the central nervous system (CNS), characterized by fusion transcripts of the RELA gene and consequent pathological activation of the NFkB pathway. These tumors represent the majority of supratentorial ependymomas in children. The validation of diagnostic tools to identify this clinically relevant ependymoma entity is essential. Here, we have used interphase fluorescent in situ hybridization (FISH) for C11orf95 and RELA, immunohistochemistry (IHC) for p65‐RelA and the recently developed DNA methylation‐based classification besides conventional histopathology, and compared the precision of the methods in 40 supratentorial pediatric brain tumors diagnosed as ependymomas in the past years. Reverse transcription PCR (RT‐PCR) and RNA sequencing were performed to explore discordant cases. Furthermore, we integrated imaging and clinical features as additional layers of information. The concordance between nuclear RelA expression by IHC and RELA FISH was 100%. Concordance between IHC and DNA methylation profiling, and between FISH and DNA methylation profiling was also high (96.4% and 95.2%, respectively). Thirty‐four out of 40 (85%) cases were confirmed by integrated diagnoses as ependymal tumors, including 22 RELA‐fused ependymomas (71% of ependymal tumors), two YAP1‐fused ependymomas (6%), six non‐RELA/non‐YAP1 ependymomas (18%) and four ependymal/subependymal mixed tumors (12%). Ependymal/subependymal mixed tumors had an excellent clinical outcome despite the presence of histopathological signs of malignancy, suggesting that these tumors should not be diagnosed as classic ependymomas. DNA methylation profiling helped in the differential diagnosis of RELA‐fused ependymomas. IHC and FISH, which are available in the majority of pathology laboratories, are valuable tools to identify RELA‐fused ependymomas. John Wiley and Sons Inc. 2018-11-28 /pmc/articles/PMC7379587/ /pubmed/30325077 http://dx.doi.org/10.1111/bpa.12664 Text en © 2018 The Authors. Brain Pathology published by John Wiley & Sons Ltd on behalf of International Society of Neuropathology https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Pagès, Mélanie Pajtler, Kristian W. Puget, Stéphanie Castel, David Boddaert, Nathalie Tauziède‐Espariat, Arnault Picot, Stéphanie Debily, Marie‐Anne Kool, Marcel Capper, David Sainte‐Rose, Christian Chrétien, Fabrice Pfister, Stefan M. Pietsch, Torsten Grill, Jacques Varlet, Pascale Andreiuolo, Felipe Diagnostics of pediatric supratentorial RELA ependymomas: integration of information from histopathology, genetics, DNA methylation and imaging |
title | Diagnostics of pediatric supratentorial RELA ependymomas: integration of information from histopathology, genetics, DNA methylation and imaging |
title_full | Diagnostics of pediatric supratentorial RELA ependymomas: integration of information from histopathology, genetics, DNA methylation and imaging |
title_fullStr | Diagnostics of pediatric supratentorial RELA ependymomas: integration of information from histopathology, genetics, DNA methylation and imaging |
title_full_unstemmed | Diagnostics of pediatric supratentorial RELA ependymomas: integration of information from histopathology, genetics, DNA methylation and imaging |
title_short | Diagnostics of pediatric supratentorial RELA ependymomas: integration of information from histopathology, genetics, DNA methylation and imaging |
title_sort | diagnostics of pediatric supratentorial rela ependymomas: integration of information from histopathology, genetics, dna methylation and imaging |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7379587/ https://www.ncbi.nlm.nih.gov/pubmed/30325077 http://dx.doi.org/10.1111/bpa.12664 |
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