Genomic landscape of high-grade meningiomas
Brain tumors: uncovering genomic disruption in meningiomas Meningiomas, which arise from the tissue surrounding the brain and spinal cord, are the most common primary brain tumor in adults. The majority of these are slow-growing and amenable to surgical resection, if treatment is indicated. However,...
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2017-04-01
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doaj-30b733f570624d2fb8c0cba27d4db8192020-12-08T13:47:37ZengNature Publishing Groupnpj Genomic Medicine2056-79442017-04-012111410.1038/s41525-017-0014-7Genomic landscape of high-grade meningiomasWenya Linda Bi0Noah F. Greenwald1Malak Abedalthagafi2Jeremiah Wala3Will J. Gibson4Pankaj K. Agarwalla5Peleg Horowitz6Steven E. Schumacher7Ekaterina Esaulova8Yu Mei9Aaron Chevalier10Matthew A. Ducar11Aaron R. Thorner12Paul van Hummelen13Anat O. Stemmer-Rachamimov14Maksym Artyomov15Ossama Al-Mefty16Gavin P. Dunn17Sandro Santagata18Ian F. Dunn19Rameen Beroukhim20Center for Skull Base and Pituitary Surgery, Department of Neurosurgery, Brigham and Women’s Hospital, Harvard Medical SchoolCenter for Skull Base and Pituitary Surgery, Department of Neurosurgery, Brigham and Women’s Hospital, Harvard Medical SchoolDivision of Neuropathology, Department of Pathology, Brigham and Women’s HospitalDepartment of Cancer Biology, Dana-Farber Cancer InstituteDepartment of Cancer Biology, Dana-Farber Cancer InstituteDepartment of Cancer Biology, Dana-Farber Cancer InstituteDepartment of Surgery, The University of ChicagoDepartment of Cancer Biology, Dana-Farber Cancer InstituteDepartment of Pathology and Immunology, Washington University School of MedicineCenter for Skull Base and Pituitary Surgery, Department of Neurosurgery, Brigham and Women’s Hospital, Harvard Medical SchoolBroad Institute of MIT and HarvardCenter for Cancer Genome Discovery, Dana-Farber Cancer InstituteCenter for Cancer Genome Discovery, Dana-Farber Cancer InstituteCenter for Cancer Genome Discovery, Dana-Farber Cancer InstituteDepartment of Pathology, Massachusetts General HospitalDepartment of Pathology and Immunology, Washington University School of MedicineCenter for Skull Base and Pituitary Surgery, Department of Neurosurgery, Brigham and Women’s Hospital, Harvard Medical SchoolDepartment of Pathology and Immunology, Washington University School of MedicineDivision of Neuropathology, Department of Pathology, Brigham and Women’s HospitalCenter for Skull Base and Pituitary Surgery, Department of Neurosurgery, Brigham and Women’s Hospital, Harvard Medical SchoolDepartment of Cancer Biology, Dana-Farber Cancer InstituteBrain tumors: uncovering genomic disruption in meningiomas Meningiomas, which arise from the tissue surrounding the brain and spinal cord, are the most common primary brain tumor in adults. The majority of these are slow-growing and amenable to surgical resection, if treatment is indicated. However, a subset of aggressive meningiomas are considered high-grade, producing significantly worse mortality. In a first study of its kind, Drs. Wenya Linda Bi, Ian Dunn, Sandro Santagata, Rameen Beroukhim, and colleagues at Harvard Medical School sequenced the genomes of 134 high-grade meningiomas and compared their makeup with lower-grade meningiomas. They found that aggressive tumors were more likely to harbor mutations in the NF2 gene and exhibit widespread genomic disruption. They also harbored an elevated rate of predicted immunogenic mutations, with implications for the use of immuno-modulatory therapies.https://doi.org/10.1038/s41525-017-0014-7 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Wenya Linda Bi Noah F. Greenwald Malak Abedalthagafi Jeremiah Wala Will J. Gibson Pankaj K. Agarwalla Peleg Horowitz Steven E. Schumacher Ekaterina Esaulova Yu Mei Aaron Chevalier Matthew A. Ducar Aaron R. Thorner Paul van Hummelen Anat O. Stemmer-Rachamimov Maksym Artyomov Ossama Al-Mefty Gavin P. Dunn Sandro Santagata Ian F. Dunn Rameen Beroukhim |
spellingShingle |
Wenya Linda Bi Noah F. Greenwald Malak Abedalthagafi Jeremiah Wala Will J. Gibson Pankaj K. Agarwalla Peleg Horowitz Steven E. Schumacher Ekaterina Esaulova Yu Mei Aaron Chevalier Matthew A. Ducar Aaron R. Thorner Paul van Hummelen Anat O. Stemmer-Rachamimov Maksym Artyomov Ossama Al-Mefty Gavin P. Dunn Sandro Santagata Ian F. Dunn Rameen Beroukhim Genomic landscape of high-grade meningiomas npj Genomic Medicine |
author_facet |
Wenya Linda Bi Noah F. Greenwald Malak Abedalthagafi Jeremiah Wala Will J. Gibson Pankaj K. Agarwalla Peleg Horowitz Steven E. Schumacher Ekaterina Esaulova Yu Mei Aaron Chevalier Matthew A. Ducar Aaron R. Thorner Paul van Hummelen Anat O. Stemmer-Rachamimov Maksym Artyomov Ossama Al-Mefty Gavin P. Dunn Sandro Santagata Ian F. Dunn Rameen Beroukhim |
author_sort |
Wenya Linda Bi |
title |
Genomic landscape of high-grade meningiomas |
title_short |
Genomic landscape of high-grade meningiomas |
title_full |
Genomic landscape of high-grade meningiomas |
title_fullStr |
Genomic landscape of high-grade meningiomas |
title_full_unstemmed |
Genomic landscape of high-grade meningiomas |
title_sort |
genomic landscape of high-grade meningiomas |
publisher |
Nature Publishing Group |
series |
npj Genomic Medicine |
issn |
2056-7944 |
publishDate |
2017-04-01 |
description |
Brain tumors: uncovering genomic disruption in meningiomas Meningiomas, which arise from the tissue surrounding the brain and spinal cord, are the most common primary brain tumor in adults. The majority of these are slow-growing and amenable to surgical resection, if treatment is indicated. However, a subset of aggressive meningiomas are considered high-grade, producing significantly worse mortality. In a first study of its kind, Drs. Wenya Linda Bi, Ian Dunn, Sandro Santagata, Rameen Beroukhim, and colleagues at Harvard Medical School sequenced the genomes of 134 high-grade meningiomas and compared their makeup with lower-grade meningiomas. They found that aggressive tumors were more likely to harbor mutations in the NF2 gene and exhibit widespread genomic disruption. They also harbored an elevated rate of predicted immunogenic mutations, with implications for the use of immuno-modulatory therapies. |
url |
https://doi.org/10.1038/s41525-017-0014-7 |
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