Timing of Smarcb1 and Nf2 inactivation determines schwannoma versus rhabdoid tumor development
SMARCB1 mutations predispose to rhabdoid tumors and schwannomas but the mechanisms underlying the tumor type specificity are unknown. Here the authors present new mouse models and show that early Smarcb1 loss causes rhabdoid tumors whereas loss at later stages combined with Nf2 gene inactivation cau...
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2017-08-01
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Series: | Nature Communications |
Online Access: | https://doi.org/10.1038/s41467-017-00346-5 |
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doaj-1faf2971b5a4423bb8a856e7f90310eb2021-01-31T12:48:47ZengNature Publishing GroupNature Communications2041-17232017-08-018111310.1038/s41467-017-00346-5Timing of Smarcb1 and Nf2 inactivation determines schwannoma versus rhabdoid tumor developmentJeremie Vitte0Fuying Gao1Giovanni Coppola2Alexander R. Judkins3Marco Giovannini4Department of Head and Neck Surgery, David Geffen School of Medicine at UCLA and Jonsson Comprehensive Cancer Center (JCCC), University of California Los AngelesSemel Institute for Neuroscience & Human Behavior and Department of Psychiatry and Biobehavioral Sciences, University of California Los AngelesSemel Institute for Neuroscience & Human Behavior and Department of Psychiatry and Biobehavioral Sciences, University of California Los AngelesDepartment of Pathology and Laboratory Medicine, Children’s Hospital Los Angeles, Keck School of Medicine, University of Southern CaliforniaDepartment of Head and Neck Surgery, David Geffen School of Medicine at UCLA and Jonsson Comprehensive Cancer Center (JCCC), University of California Los AngelesSMARCB1 mutations predispose to rhabdoid tumors and schwannomas but the mechanisms underlying the tumor type specificity are unknown. Here the authors present new mouse models and show that early Smarcb1 loss causes rhabdoid tumors whereas loss at later stages combined with Nf2 gene inactivation causes shwannomas.https://doi.org/10.1038/s41467-017-00346-5 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jeremie Vitte Fuying Gao Giovanni Coppola Alexander R. Judkins Marco Giovannini |
spellingShingle |
Jeremie Vitte Fuying Gao Giovanni Coppola Alexander R. Judkins Marco Giovannini Timing of Smarcb1 and Nf2 inactivation determines schwannoma versus rhabdoid tumor development Nature Communications |
author_facet |
Jeremie Vitte Fuying Gao Giovanni Coppola Alexander R. Judkins Marco Giovannini |
author_sort |
Jeremie Vitte |
title |
Timing of Smarcb1 and Nf2 inactivation determines schwannoma versus rhabdoid tumor development |
title_short |
Timing of Smarcb1 and Nf2 inactivation determines schwannoma versus rhabdoid tumor development |
title_full |
Timing of Smarcb1 and Nf2 inactivation determines schwannoma versus rhabdoid tumor development |
title_fullStr |
Timing of Smarcb1 and Nf2 inactivation determines schwannoma versus rhabdoid tumor development |
title_full_unstemmed |
Timing of Smarcb1 and Nf2 inactivation determines schwannoma versus rhabdoid tumor development |
title_sort |
timing of smarcb1 and nf2 inactivation determines schwannoma versus rhabdoid tumor development |
publisher |
Nature Publishing Group |
series |
Nature Communications |
issn |
2041-1723 |
publishDate |
2017-08-01 |
description |
SMARCB1 mutations predispose to rhabdoid tumors and schwannomas but the mechanisms underlying the tumor type specificity are unknown. Here the authors present new mouse models and show that early Smarcb1 loss causes rhabdoid tumors whereas loss at later stages combined with Nf2 gene inactivation causes shwannomas. |
url |
https://doi.org/10.1038/s41467-017-00346-5 |
work_keys_str_mv |
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