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Inversion-mediated gene fusions involving NAB2-STAT6 in an unusual malignant meningioma
BACKGROUND: Meningiomas are the most common primary intracranial tumours, with ∼3% meeting current histopathologic criteria for malignancy. METHODS: In this study, we explored the transcriptome of meningiomas using RNA-Seq. RESULTS: Inversion-mediated fusions between two adjacent genes, NAB2 and STA...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3749567/ https://www.ncbi.nlm.nih.gov/pubmed/23860521 http://dx.doi.org/10.1038/bjc.2013.395 |
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author | Gao, F Ling, C Shi, L Commins, D Zada, G Mack, W J Wang, K |
author_facet | Gao, F Ling, C Shi, L Commins, D Zada, G Mack, W J Wang, K |
author_sort | Gao, F |
collection | PubMed |
description | BACKGROUND: Meningiomas are the most common primary intracranial tumours, with ∼3% meeting current histopathologic criteria for malignancy. METHODS: In this study, we explored the transcriptome of meningiomas using RNA-Seq. RESULTS: Inversion-mediated fusions between two adjacent genes, NAB2 and STAT6, were detected in one malignant tumour, creating two novel in-frame transcripts that were validated by RT–PCR and Sanger sequencing. CONCLUSION: Gene fusions of NAB2-STAT6 were recently implicated in the pathogenesis of solitary fibrous tumours; our study suggested that similar fusions may also have a role in a malignant meningioma with unusual histopathologic features. |
format | Online Article Text |
id | pubmed-3749567 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-37495672014-08-20 Inversion-mediated gene fusions involving NAB2-STAT6 in an unusual malignant meningioma Gao, F Ling, C Shi, L Commins, D Zada, G Mack, W J Wang, K Br J Cancer Short Communication BACKGROUND: Meningiomas are the most common primary intracranial tumours, with ∼3% meeting current histopathologic criteria for malignancy. METHODS: In this study, we explored the transcriptome of meningiomas using RNA-Seq. RESULTS: Inversion-mediated fusions between two adjacent genes, NAB2 and STAT6, were detected in one malignant tumour, creating two novel in-frame transcripts that were validated by RT–PCR and Sanger sequencing. CONCLUSION: Gene fusions of NAB2-STAT6 were recently implicated in the pathogenesis of solitary fibrous tumours; our study suggested that similar fusions may also have a role in a malignant meningioma with unusual histopathologic features. Nature Publishing Group 2013-08-20 2013-07-16 /pmc/articles/PMC3749567/ /pubmed/23860521 http://dx.doi.org/10.1038/bjc.2013.395 Text en Copyright © 2013 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/3.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/ |
spellingShingle | Short Communication Gao, F Ling, C Shi, L Commins, D Zada, G Mack, W J Wang, K Inversion-mediated gene fusions involving NAB2-STAT6 in an unusual malignant meningioma |
title | Inversion-mediated gene fusions involving NAB2-STAT6 in an unusual malignant meningioma |
title_full | Inversion-mediated gene fusions involving NAB2-STAT6 in an unusual malignant meningioma |
title_fullStr | Inversion-mediated gene fusions involving NAB2-STAT6 in an unusual malignant meningioma |
title_full_unstemmed | Inversion-mediated gene fusions involving NAB2-STAT6 in an unusual malignant meningioma |
title_short | Inversion-mediated gene fusions involving NAB2-STAT6 in an unusual malignant meningioma |
title_sort | inversion-mediated gene fusions involving nab2-stat6 in an unusual malignant meningioma |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3749567/ https://www.ncbi.nlm.nih.gov/pubmed/23860521 http://dx.doi.org/10.1038/bjc.2013.395 |
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