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Molecular and immunophenotypic characterization of SMARCB1 (INI1) - deficient intrathoracic Neoplasms
The switch/sucrose-non-fermenting (SWI/SNF) complex is an ATP-dependent chromatin remodeling complex that plays important roles in DNA repair, transcription and cell differentiation. This complex consists of multiple subunits and is of particular interest in thoracic malignancies due to frequent sub...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group US
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9708576/ https://www.ncbi.nlm.nih.gov/pubmed/35864317 http://dx.doi.org/10.1038/s41379-022-01133-4 |
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author | Haberecker, Martina Bühler, Marco Matteo Mendieta, Alicia Pliego Guggenberger, Roman Arnold, Fabian Markert, Eva Rechsteiner, Markus Zoche, Martin Britschgi, Christian Pauli, Chantal |
author_facet | Haberecker, Martina Bühler, Marco Matteo Mendieta, Alicia Pliego Guggenberger, Roman Arnold, Fabian Markert, Eva Rechsteiner, Markus Zoche, Martin Britschgi, Christian Pauli, Chantal |
author_sort | Haberecker, Martina |
collection | PubMed |
description | The switch/sucrose-non-fermenting (SWI/SNF) complex is an ATP-dependent chromatin remodeling complex that plays important roles in DNA repair, transcription and cell differentiation. This complex consists of multiple subunits and is of particular interest in thoracic malignancies due to frequent subunit alteration of SMARCA4 (BRG1). Much less is known about SMARCB1 (INI1) deficient intrathoracic neoplasms, which are rare, often misclassified and understudied. In a retrospective analysis of 1479 intrathoracic malignant neoplasms using immunohistochemistry for INI1 (SMARCB1) on tissue micro arrays (TMA) and a search through our hospital sarcoma database, we identified in total nine intrathoracic, INI1 deficient cases (n = 9). We characterized these cases further by additional immunohistochemistry, broad targeted genomic analysis, methylation profiling and correlated them with clinical and radiological data. This showed that genomic SMARCB1 together with tumor suppressor alterations drive tumorigenesis in some of these cases, rather than epigenetic changes such as DNA methylation. A proper diagnostic classification, however, remains challenging. Intrathoracic tumors with loss or alteration of SMARCB1 (INI1) are highly aggressive and remain often underdiagnosed due to their rarity, which leads to false diagnostic interpretations. A better understanding of these tumors and proper diagnosis is important for better patient care as clinical trials and more targeted therapeutic options are emerging. |
format | Online Article Text |
id | pubmed-9708576 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group US |
record_format | MEDLINE/PubMed |
spelling | pubmed-97085762022-12-01 Molecular and immunophenotypic characterization of SMARCB1 (INI1) - deficient intrathoracic Neoplasms Haberecker, Martina Bühler, Marco Matteo Mendieta, Alicia Pliego Guggenberger, Roman Arnold, Fabian Markert, Eva Rechsteiner, Markus Zoche, Martin Britschgi, Christian Pauli, Chantal Mod Pathol Article The switch/sucrose-non-fermenting (SWI/SNF) complex is an ATP-dependent chromatin remodeling complex that plays important roles in DNA repair, transcription and cell differentiation. This complex consists of multiple subunits and is of particular interest in thoracic malignancies due to frequent subunit alteration of SMARCA4 (BRG1). Much less is known about SMARCB1 (INI1) deficient intrathoracic neoplasms, which are rare, often misclassified and understudied. In a retrospective analysis of 1479 intrathoracic malignant neoplasms using immunohistochemistry for INI1 (SMARCB1) on tissue micro arrays (TMA) and a search through our hospital sarcoma database, we identified in total nine intrathoracic, INI1 deficient cases (n = 9). We characterized these cases further by additional immunohistochemistry, broad targeted genomic analysis, methylation profiling and correlated them with clinical and radiological data. This showed that genomic SMARCB1 together with tumor suppressor alterations drive tumorigenesis in some of these cases, rather than epigenetic changes such as DNA methylation. A proper diagnostic classification, however, remains challenging. Intrathoracic tumors with loss or alteration of SMARCB1 (INI1) are highly aggressive and remain often underdiagnosed due to their rarity, which leads to false diagnostic interpretations. A better understanding of these tumors and proper diagnosis is important for better patient care as clinical trials and more targeted therapeutic options are emerging. Nature Publishing Group US 2022-07-21 2022 /pmc/articles/PMC9708576/ /pubmed/35864317 http://dx.doi.org/10.1038/s41379-022-01133-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Haberecker, Martina Bühler, Marco Matteo Mendieta, Alicia Pliego Guggenberger, Roman Arnold, Fabian Markert, Eva Rechsteiner, Markus Zoche, Martin Britschgi, Christian Pauli, Chantal Molecular and immunophenotypic characterization of SMARCB1 (INI1) - deficient intrathoracic Neoplasms |
title | Molecular and immunophenotypic characterization of SMARCB1 (INI1) - deficient intrathoracic Neoplasms |
title_full | Molecular and immunophenotypic characterization of SMARCB1 (INI1) - deficient intrathoracic Neoplasms |
title_fullStr | Molecular and immunophenotypic characterization of SMARCB1 (INI1) - deficient intrathoracic Neoplasms |
title_full_unstemmed | Molecular and immunophenotypic characterization of SMARCB1 (INI1) - deficient intrathoracic Neoplasms |
title_short | Molecular and immunophenotypic characterization of SMARCB1 (INI1) - deficient intrathoracic Neoplasms |
title_sort | molecular and immunophenotypic characterization of smarcb1 (ini1) - deficient intrathoracic neoplasms |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9708576/ https://www.ncbi.nlm.nih.gov/pubmed/35864317 http://dx.doi.org/10.1038/s41379-022-01133-4 |
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