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Identification of ETV6-RUNX1-like and DUX4-rearranged subtypes in paediatric B-cell precursor acute lymphoblastic leukaemia
Fusion genes are potent driver mutations in cancer. In this study, we delineate the fusion gene landscape in a consecutive series of 195 paediatric B-cell precursor acute lymphoblastic leukaemia (BCP ALL). Using RNA sequencing, we find in-frame fusion genes in 127 (65%) cases, including 27 novel fus...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4897744/ https://www.ncbi.nlm.nih.gov/pubmed/27265895 http://dx.doi.org/10.1038/ncomms11790 |
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author | Lilljebjörn, Henrik Henningsson, Rasmus Hyrenius-Wittsten, Axel Olsson, Linda Orsmark-Pietras, Christina von Palffy, Sofia Askmyr, Maria Rissler, Marianne Schrappe, Martin Cario, Gunnar Castor, Anders Pronk, Cornelis J. H. Behrendtz, Mikael Mitelman, Felix Johansson, Bertil Paulsson, Kajsa Andersson, Anna K. Fontes, Magnus Fioretos, Thoas |
author_facet | Lilljebjörn, Henrik Henningsson, Rasmus Hyrenius-Wittsten, Axel Olsson, Linda Orsmark-Pietras, Christina von Palffy, Sofia Askmyr, Maria Rissler, Marianne Schrappe, Martin Cario, Gunnar Castor, Anders Pronk, Cornelis J. H. Behrendtz, Mikael Mitelman, Felix Johansson, Bertil Paulsson, Kajsa Andersson, Anna K. Fontes, Magnus Fioretos, Thoas |
author_sort | Lilljebjörn, Henrik |
collection | PubMed |
description | Fusion genes are potent driver mutations in cancer. In this study, we delineate the fusion gene landscape in a consecutive series of 195 paediatric B-cell precursor acute lymphoblastic leukaemia (BCP ALL). Using RNA sequencing, we find in-frame fusion genes in 127 (65%) cases, including 27 novel fusions. We describe a subtype characterized by recurrent IGH-DUX4 or ERG-DUX4 fusions, representing 4% of cases, leading to overexpression of DUX4 and frequently co-occurring with intragenic ERG deletions. Furthermore, we identify a subtype characterized by an ETV6-RUNX1-like gene-expression profile and coexisting ETV6 and IKZF1 alterations. Thus, this study provides a detailed overview of fusion genes in paediatric BCP ALL and adds new pathogenetic insights, which may improve risk stratification and provide therapeutic options for this disease. |
format | Online Article Text |
id | pubmed-4897744 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48977442016-06-21 Identification of ETV6-RUNX1-like and DUX4-rearranged subtypes in paediatric B-cell precursor acute lymphoblastic leukaemia Lilljebjörn, Henrik Henningsson, Rasmus Hyrenius-Wittsten, Axel Olsson, Linda Orsmark-Pietras, Christina von Palffy, Sofia Askmyr, Maria Rissler, Marianne Schrappe, Martin Cario, Gunnar Castor, Anders Pronk, Cornelis J. H. Behrendtz, Mikael Mitelman, Felix Johansson, Bertil Paulsson, Kajsa Andersson, Anna K. Fontes, Magnus Fioretos, Thoas Nat Commun Article Fusion genes are potent driver mutations in cancer. In this study, we delineate the fusion gene landscape in a consecutive series of 195 paediatric B-cell precursor acute lymphoblastic leukaemia (BCP ALL). Using RNA sequencing, we find in-frame fusion genes in 127 (65%) cases, including 27 novel fusions. We describe a subtype characterized by recurrent IGH-DUX4 or ERG-DUX4 fusions, representing 4% of cases, leading to overexpression of DUX4 and frequently co-occurring with intragenic ERG deletions. Furthermore, we identify a subtype characterized by an ETV6-RUNX1-like gene-expression profile and coexisting ETV6 and IKZF1 alterations. Thus, this study provides a detailed overview of fusion genes in paediatric BCP ALL and adds new pathogenetic insights, which may improve risk stratification and provide therapeutic options for this disease. Nature Publishing Group 2016-06-06 /pmc/articles/PMC4897744/ /pubmed/27265895 http://dx.doi.org/10.1038/ncomms11790 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Lilljebjörn, Henrik Henningsson, Rasmus Hyrenius-Wittsten, Axel Olsson, Linda Orsmark-Pietras, Christina von Palffy, Sofia Askmyr, Maria Rissler, Marianne Schrappe, Martin Cario, Gunnar Castor, Anders Pronk, Cornelis J. H. Behrendtz, Mikael Mitelman, Felix Johansson, Bertil Paulsson, Kajsa Andersson, Anna K. Fontes, Magnus Fioretos, Thoas Identification of ETV6-RUNX1-like and DUX4-rearranged subtypes in paediatric B-cell precursor acute lymphoblastic leukaemia |
title | Identification of ETV6-RUNX1-like and DUX4-rearranged subtypes in paediatric B-cell precursor acute lymphoblastic leukaemia |
title_full | Identification of ETV6-RUNX1-like and DUX4-rearranged subtypes in paediatric B-cell precursor acute lymphoblastic leukaemia |
title_fullStr | Identification of ETV6-RUNX1-like and DUX4-rearranged subtypes in paediatric B-cell precursor acute lymphoblastic leukaemia |
title_full_unstemmed | Identification of ETV6-RUNX1-like and DUX4-rearranged subtypes in paediatric B-cell precursor acute lymphoblastic leukaemia |
title_short | Identification of ETV6-RUNX1-like and DUX4-rearranged subtypes in paediatric B-cell precursor acute lymphoblastic leukaemia |
title_sort | identification of etv6-runx1-like and dux4-rearranged subtypes in paediatric b-cell precursor acute lymphoblastic leukaemia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4897744/ https://www.ncbi.nlm.nih.gov/pubmed/27265895 http://dx.doi.org/10.1038/ncomms11790 |
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