Skip to main content
Top
Published in: Acta Neuropathologica 3/2015

01-09-2015 | Correspondence

High frequency of H3F3A K27M mutations characterizes pediatric and adult high-grade gliomas of the spinal cord

Authors: Marco Gessi, Gerrit H. Gielen, Verena Dreschmann, Andreas Waha, Torsten Pietsch

Published in: Acta Neuropathologica | Issue 3/2015

Login to get access

Excerpt

Diffuse high-grade gliomas (HGG) in the spinal cord are rare [5]. It is still undetermined whether they could share genetic alterations with their supratentorial counterparts: in particular, because the spinal cord has to be considered a midline structure, a high incidence of H3F3A K27M mutations could be hypothesized, as reported in diffuse pontine gliomas (DIPG) and in pediatric midline HGG [13, 68]. In this study, we investigated the H3F3A K27M status of 30 primary spinal HGG affecting pediatric and adult patients. …
Appendix
Available only for authorised users
Literature
1.
go back to reference Aihara K, Mukasa A, Gotoh K, Saito K, Nagae G, Tsuji S et al (2014) H3F3A K27M mutations in thalamic gliomas from young adult patients. Neuro Oncol 16:140–146CrossRefPubMedPubMedCentral Aihara K, Mukasa A, Gotoh K, Saito K, Nagae G, Tsuji S et al (2014) H3F3A K27M mutations in thalamic gliomas from young adult patients. Neuro Oncol 16:140–146CrossRefPubMedPubMedCentral
2.
go back to reference Bender S, Tang Y, Lindroth AM, Hovestadt V, Jones DT, Kool M et al (2013) Reduced H3K27me3 and DNA hypomethylation are major drivers of gene expression in K27M mutant pediatric high-grade gliomas. Cancer Cell 24:660–672CrossRefPubMed Bender S, Tang Y, Lindroth AM, Hovestadt V, Jones DT, Kool M et al (2013) Reduced H3K27me3 and DNA hypomethylation are major drivers of gene expression in K27M mutant pediatric high-grade gliomas. Cancer Cell 24:660–672CrossRefPubMed
3.
go back to reference Buczkowicz P, Bartels U, Bouffet E, Becher O, Hawkins C (2014) Histopathological spectrum of paediatric diffuse intrinsic pontine glioma: diagnostic and therapeutic implications. Acta Neuropathol 128:573–581CrossRefPubMedPubMedCentral Buczkowicz P, Bartels U, Bouffet E, Becher O, Hawkins C (2014) Histopathological spectrum of paediatric diffuse intrinsic pontine glioma: diagnostic and therapeutic implications. Acta Neuropathol 128:573–581CrossRefPubMedPubMedCentral
4.
go back to reference Gielen GH, Gessi M, Buttarelli FR, Baldi C, Hammes J, Zur Muehlen A et al (2015) Genetic analysis of diffuse high-grade astrocytomas in infancy defines a novel molecular entity. Brain Pathol 25:409–417CrossRefPubMed Gielen GH, Gessi M, Buttarelli FR, Baldi C, Hammes J, Zur Muehlen A et al (2015) Genetic analysis of diffuse high-grade astrocytomas in infancy defines a novel molecular entity. Brain Pathol 25:409–417CrossRefPubMed
5.
go back to reference Louis DN, Ohgaki H, Wiestler OD, Cavanee WK (2007) WHO classification of tumors of the central nervous system. IARC press, Lyon Louis DN, Ohgaki H, Wiestler OD, Cavanee WK (2007) WHO classification of tumors of the central nervous system. IARC press, Lyon
6.
go back to reference Reyes-Botero G, Giry M, Mokhtari K, Labussière M, Idbaih A, Delattre JY et al (2014) Molecular analysis of diffuse intrinsic brainstem gliomas in adults. J Neurooncol 116:405–411CrossRefPubMed Reyes-Botero G, Giry M, Mokhtari K, Labussière M, Idbaih A, Delattre JY et al (2014) Molecular analysis of diffuse intrinsic brainstem gliomas in adults. J Neurooncol 116:405–411CrossRefPubMed
7.
go back to reference Schwartzentruber J, Korshunov A, Liu XY, Jones DT, Pfaff E, Jacob K et al (2012) Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma. Nature 482:226–231CrossRefPubMed Schwartzentruber J, Korshunov A, Liu XY, Jones DT, Pfaff E, Jacob K et al (2012) Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma. Nature 482:226–231CrossRefPubMed
8.
go back to reference Sturm D, Witt H, Hovestadt V, Khuong-Quang DA, Jones DT, Konermann C et al (2012) Hotspot mutations in H3F3A and IDH1 define distinct epigenetic and biological subgroups of glioblastoma. Cancer Cell 22:425–437CrossRefPubMed Sturm D, Witt H, Hovestadt V, Khuong-Quang DA, Jones DT, Konermann C et al (2012) Hotspot mutations in H3F3A and IDH1 define distinct epigenetic and biological subgroups of glioblastoma. Cancer Cell 22:425–437CrossRefPubMed
9.
go back to reference Yuen BT, Knoepfler PS (2013) Histone H3.3 mutations: a variant path to cancer. Cancer Cell 24:567–574CrossRefPubMed Yuen BT, Knoepfler PS (2013) Histone H3.3 mutations: a variant path to cancer. Cancer Cell 24:567–574CrossRefPubMed
Metadata
Title
High frequency of H3F3A K27M mutations characterizes pediatric and adult high-grade gliomas of the spinal cord
Authors
Marco Gessi
Gerrit H. Gielen
Verena Dreschmann
Andreas Waha
Torsten Pietsch
Publication date
01-09-2015
Publisher
Springer Berlin Heidelberg
Published in
Acta Neuropathologica / Issue 3/2015
Print ISSN: 0001-6322
Electronic ISSN: 1432-0533
DOI
https://doi.org/10.1007/s00401-015-1463-7

Other articles of this Issue 3/2015

Acta Neuropathologica 3/2015 Go to the issue