Current molecular understanding of central nervous system schwannomas

Abstract Background Schwannomas are tumors that originate from myelinating Schwann cells and can occur in cranial, spinal, and peripheral nerves. Although our understanding of the molecular biology underlying schwannomas remains incomplete, numerous studies have identified various molecular findings...

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Main Authors: Takahiro Tsuchiya, Satoru Miyawaki, Yu Teranishi, Kenta Ohara, Yudai Hirano, Shotaro Ogawa, Seiei Torazawa, Yu Sakai, Hiroki Hongo, Hideaki Ono, Nobuhito Saito
Format: Article
Language:English
Published: BMC 2025-02-01
Series:Acta Neuropathologica Communications
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Online Access:https://doi.org/10.1186/s40478-025-01937-w
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author Takahiro Tsuchiya
Satoru Miyawaki
Yu Teranishi
Kenta Ohara
Yudai Hirano
Shotaro Ogawa
Seiei Torazawa
Yu Sakai
Hiroki Hongo
Hideaki Ono
Nobuhito Saito
author_facet Takahiro Tsuchiya
Satoru Miyawaki
Yu Teranishi
Kenta Ohara
Yudai Hirano
Shotaro Ogawa
Seiei Torazawa
Yu Sakai
Hiroki Hongo
Hideaki Ono
Nobuhito Saito
author_sort Takahiro Tsuchiya
collection DOAJ
description Abstract Background Schwannomas are tumors that originate from myelinating Schwann cells and can occur in cranial, spinal, and peripheral nerves. Although our understanding of the molecular biology underlying schwannomas remains incomplete, numerous studies have identified various molecular findings and biomarkers associated with schwannomas of the central nervous system (CNS). The development of these tumors is primarily linked to mutations in the NF2 gene. Merlin, the protein encoded by NF2, is integral to several signaling pathways, including Ras/Raf/MEK/ERK, PI3K/Akt/mTORC1, Wnt/β-catenin, and the Hippo pathway. Main body Recent research has also uncovered novel genetic alterations, such as the SH3PXD2A::HTRA1 fusion gene, VGLL-fusions in intraparenchymal CNS schwannomas, and the SOX10 mutation particularly in non-vestibular cranial nerve schwannomas. In addition to genetic alterations, research is also being conducted on gene expression and epigenetic regulation, with a focus on NF2 methylation and post-transcriptional silencing by micro RNA. Furthermore, the advent of advanced techniques like single-cell sequencing and multi-omics analysis has facilitated rapid discoveries related to the tumor microenvironment and tumor heterogeneity in schwannomas. Conclusion A deeper exploration of these molecular findings could clarify the mechanisms of schwannoma tumorigenesis and progression, ultimately guiding the development of new therapeutic targets. This review offers a comprehensive overview of the current molecular understanding of CNS schwannomas, emphasizing the insights gained from previous research, while addressing existing controversies and outlining future research and treatment perspectives.
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spelling doaj-art-9ca3f2c64427435bb72fca5ad0938b432025-02-09T12:59:17ZengBMCActa Neuropathologica Communications2051-59602025-02-0113111710.1186/s40478-025-01937-wCurrent molecular understanding of central nervous system schwannomasTakahiro Tsuchiya0Satoru Miyawaki1Yu Teranishi2Kenta Ohara3Yudai Hirano4Shotaro Ogawa5Seiei Torazawa6Yu Sakai7Hiroki Hongo8Hideaki Ono9Nobuhito Saito10Department of Neurosurgery, Faculty of Medicine, The University of TokyoDepartment of Neurosurgery, Faculty of Medicine, The University of TokyoDepartment of Neurosurgery, Faculty of Medicine, The University of TokyoDepartment of Neurosurgery, Faculty of Medicine, The University of TokyoDepartment of Neurosurgery, Faculty of Medicine, The University of TokyoDepartment of Neurosurgery, Faculty of Medicine, The University of TokyoDepartment of Neurosurgery, Faculty of Medicine, The University of TokyoDepartment of Neurosurgery, Faculty of Medicine, The University of TokyoDepartment of Neurosurgery, Faculty of Medicine, The University of TokyoDepartment of Neurosurgery, Faculty of Medicine, The University of TokyoDepartment of Neurosurgery, Faculty of Medicine, The University of TokyoAbstract Background Schwannomas are tumors that originate from myelinating Schwann cells and can occur in cranial, spinal, and peripheral nerves. Although our understanding of the molecular biology underlying schwannomas remains incomplete, numerous studies have identified various molecular findings and biomarkers associated with schwannomas of the central nervous system (CNS). The development of these tumors is primarily linked to mutations in the NF2 gene. Merlin, the protein encoded by NF2, is integral to several signaling pathways, including Ras/Raf/MEK/ERK, PI3K/Akt/mTORC1, Wnt/β-catenin, and the Hippo pathway. Main body Recent research has also uncovered novel genetic alterations, such as the SH3PXD2A::HTRA1 fusion gene, VGLL-fusions in intraparenchymal CNS schwannomas, and the SOX10 mutation particularly in non-vestibular cranial nerve schwannomas. In addition to genetic alterations, research is also being conducted on gene expression and epigenetic regulation, with a focus on NF2 methylation and post-transcriptional silencing by micro RNA. Furthermore, the advent of advanced techniques like single-cell sequencing and multi-omics analysis has facilitated rapid discoveries related to the tumor microenvironment and tumor heterogeneity in schwannomas. Conclusion A deeper exploration of these molecular findings could clarify the mechanisms of schwannoma tumorigenesis and progression, ultimately guiding the development of new therapeutic targets. This review offers a comprehensive overview of the current molecular understanding of CNS schwannomas, emphasizing the insights gained from previous research, while addressing existing controversies and outlining future research and treatment perspectives.https://doi.org/10.1186/s40478-025-01937-wSchwannomaCentral nervous systemMolecularGenetic alterationGene expressionEpigenetics
spellingShingle Takahiro Tsuchiya
Satoru Miyawaki
Yu Teranishi
Kenta Ohara
Yudai Hirano
Shotaro Ogawa
Seiei Torazawa
Yu Sakai
Hiroki Hongo
Hideaki Ono
Nobuhito Saito
Current molecular understanding of central nervous system schwannomas
Acta Neuropathologica Communications
Schwannoma
Central nervous system
Molecular
Genetic alteration
Gene expression
Epigenetics
title Current molecular understanding of central nervous system schwannomas
title_full Current molecular understanding of central nervous system schwannomas
title_fullStr Current molecular understanding of central nervous system schwannomas
title_full_unstemmed Current molecular understanding of central nervous system schwannomas
title_short Current molecular understanding of central nervous system schwannomas
title_sort current molecular understanding of central nervous system schwannomas
topic Schwannoma
Central nervous system
Molecular
Genetic alteration
Gene expression
Epigenetics
url https://doi.org/10.1186/s40478-025-01937-w
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