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Histone 3.3 hotspot mutations in conventional osteosarcomas: a comprehensive clinical and molecular characterization of six H3F3A mutated cases
BACKGROUND: Histone 3.3 (H3.3) hotspot mutations in bone tumors occur in the vast majority of giant cell tumors of bone (GCTBs; 96%), chondroblastomas (95%) and in a few cases of osteosarcomas. However, clinical presentation, histopathological features, and additional molecular characteristics of H3...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5418758/ https://www.ncbi.nlm.nih.gov/pubmed/28484590 http://dx.doi.org/10.1186/s13569-017-0075-5 |
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author | Koelsche, Christian Schrimpf, Daniel Tharun, Lars Roth, Eva Sturm, Dominik Jones, David T. W. Renker, Eva-Kristin Sill, Martin Baude, Annika Sahm, Felix Capper, David Bewerunge-Hudler, Melanie Hartmann, Wolfgang Kulozik, Andreas E. Petersen, Iver Flucke, Uta Schreuder, Hendrik W. B. Büttner, Reinhard Weber, Marc-André Schirmacher, Peter Plass, Christoph Pfister, Stefan M. von Deimling, Andreas Mechtersheimer, Gunhild |
author_facet | Koelsche, Christian Schrimpf, Daniel Tharun, Lars Roth, Eva Sturm, Dominik Jones, David T. W. Renker, Eva-Kristin Sill, Martin Baude, Annika Sahm, Felix Capper, David Bewerunge-Hudler, Melanie Hartmann, Wolfgang Kulozik, Andreas E. Petersen, Iver Flucke, Uta Schreuder, Hendrik W. B. Büttner, Reinhard Weber, Marc-André Schirmacher, Peter Plass, Christoph Pfister, Stefan M. von Deimling, Andreas Mechtersheimer, Gunhild |
author_sort | Koelsche, Christian |
collection | PubMed |
description | BACKGROUND: Histone 3.3 (H3.3) hotspot mutations in bone tumors occur in the vast majority of giant cell tumors of bone (GCTBs; 96%), chondroblastomas (95%) and in a few cases of osteosarcomas. However, clinical presentation, histopathological features, and additional molecular characteristics of H3.3 mutant osteosarcomas are largely unknown. METHODS: In this multicentre, retrospective study, a total of 106 conventional high-grade osteosarcomas, across all age groups were re-examined for hotspot mutations in the H3.3 coding genes H3F3A and H3F3B. H3.3 mutant osteosarcomas were re-evaluated in a multidisciplinary manner and analyzed for genome-wide DNA-methylation patterns and DNA copy number aberrations alongside H3.3 wild-type osteosarcomas and H3F3A G34W/L mutant GCTBs. RESULTS: Six osteosarcomas (6/106) carried H3F3A hotspot mutations. No mutations were found in H3F3B. All patients with H3F3A mutant osteosarcoma were older than 30 years with a median age of 65 years. Copy number aberrations that are commonly encountered in high-grade osteosarcomas also occurred in H3F3A mutant osteosarcomas. Unlike a single osteosarcoma with a H3F3A K27M mutation, the DNA methylation profiles of H3F3A G34W/R mutant osteosarcomas were clearly different from H3.3 wild-type osteosarcomas, but more closely related to GCTBs. The most differentially methylated promoters between H3F3A G34W/R mutant and H3.3 wild-type osteosarcomas were in KLLN/PTEN (p < 0.00005) and HIST1H2BB (p < 0.0005). CONCLUSIONS: H3.3 mutations in osteosarcomas may occur in H3F3A at mutational hotspots. They are overall rare, but become more frequent in osteosarcoma patients older than 30 years. Osteosarcomas carrying H3F3A G34W/R mutations are associated with epigenetic dysregulation of KLLN/PTEN and HIST1H2BB. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13569-017-0075-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5418758 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-54187582017-05-08 Histone 3.3 hotspot mutations in conventional osteosarcomas: a comprehensive clinical and molecular characterization of six H3F3A mutated cases Koelsche, Christian Schrimpf, Daniel Tharun, Lars Roth, Eva Sturm, Dominik Jones, David T. W. Renker, Eva-Kristin Sill, Martin Baude, Annika Sahm, Felix Capper, David Bewerunge-Hudler, Melanie Hartmann, Wolfgang Kulozik, Andreas E. Petersen, Iver Flucke, Uta Schreuder, Hendrik W. B. Büttner, Reinhard Weber, Marc-André Schirmacher, Peter Plass, Christoph Pfister, Stefan M. von Deimling, Andreas Mechtersheimer, Gunhild Clin Sarcoma Res Research BACKGROUND: Histone 3.3 (H3.3) hotspot mutations in bone tumors occur in the vast majority of giant cell tumors of bone (GCTBs; 96%), chondroblastomas (95%) and in a few cases of osteosarcomas. However, clinical presentation, histopathological features, and additional molecular characteristics of H3.3 mutant osteosarcomas are largely unknown. METHODS: In this multicentre, retrospective study, a total of 106 conventional high-grade osteosarcomas, across all age groups were re-examined for hotspot mutations in the H3.3 coding genes H3F3A and H3F3B. H3.3 mutant osteosarcomas were re-evaluated in a multidisciplinary manner and analyzed for genome-wide DNA-methylation patterns and DNA copy number aberrations alongside H3.3 wild-type osteosarcomas and H3F3A G34W/L mutant GCTBs. RESULTS: Six osteosarcomas (6/106) carried H3F3A hotspot mutations. No mutations were found in H3F3B. All patients with H3F3A mutant osteosarcoma were older than 30 years with a median age of 65 years. Copy number aberrations that are commonly encountered in high-grade osteosarcomas also occurred in H3F3A mutant osteosarcomas. Unlike a single osteosarcoma with a H3F3A K27M mutation, the DNA methylation profiles of H3F3A G34W/R mutant osteosarcomas were clearly different from H3.3 wild-type osteosarcomas, but more closely related to GCTBs. The most differentially methylated promoters between H3F3A G34W/R mutant and H3.3 wild-type osteosarcomas were in KLLN/PTEN (p < 0.00005) and HIST1H2BB (p < 0.0005). CONCLUSIONS: H3.3 mutations in osteosarcomas may occur in H3F3A at mutational hotspots. They are overall rare, but become more frequent in osteosarcoma patients older than 30 years. Osteosarcomas carrying H3F3A G34W/R mutations are associated with epigenetic dysregulation of KLLN/PTEN and HIST1H2BB. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13569-017-0075-5) contains supplementary material, which is available to authorized users. BioMed Central 2017-05-04 /pmc/articles/PMC5418758/ /pubmed/28484590 http://dx.doi.org/10.1186/s13569-017-0075-5 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Koelsche, Christian Schrimpf, Daniel Tharun, Lars Roth, Eva Sturm, Dominik Jones, David T. W. Renker, Eva-Kristin Sill, Martin Baude, Annika Sahm, Felix Capper, David Bewerunge-Hudler, Melanie Hartmann, Wolfgang Kulozik, Andreas E. Petersen, Iver Flucke, Uta Schreuder, Hendrik W. B. Büttner, Reinhard Weber, Marc-André Schirmacher, Peter Plass, Christoph Pfister, Stefan M. von Deimling, Andreas Mechtersheimer, Gunhild Histone 3.3 hotspot mutations in conventional osteosarcomas: a comprehensive clinical and molecular characterization of six H3F3A mutated cases |
title | Histone 3.3 hotspot mutations in conventional osteosarcomas: a comprehensive clinical and molecular characterization of six H3F3A mutated cases |
title_full | Histone 3.3 hotspot mutations in conventional osteosarcomas: a comprehensive clinical and molecular characterization of six H3F3A mutated cases |
title_fullStr | Histone 3.3 hotspot mutations in conventional osteosarcomas: a comprehensive clinical and molecular characterization of six H3F3A mutated cases |
title_full_unstemmed | Histone 3.3 hotspot mutations in conventional osteosarcomas: a comprehensive clinical and molecular characterization of six H3F3A mutated cases |
title_short | Histone 3.3 hotspot mutations in conventional osteosarcomas: a comprehensive clinical and molecular characterization of six H3F3A mutated cases |
title_sort | histone 3.3 hotspot mutations in conventional osteosarcomas: a comprehensive clinical and molecular characterization of six h3f3a mutated cases |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5418758/ https://www.ncbi.nlm.nih.gov/pubmed/28484590 http://dx.doi.org/10.1186/s13569-017-0075-5 |
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