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Usp9X Regulates Cell Death in Malignant Peripheral Nerve Sheath Tumors
Malignant peripheral nerve sheath tumors (MPNSTs) are the leading cause of death in neurofibromatosis type 1 (NF1) patients. Current treatment modalities have been largely unsuccessful in improving MPNST patient survival, making the identification of new therapeutic targets urgent. In this study, we...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6255814/ https://www.ncbi.nlm.nih.gov/pubmed/30478285 http://dx.doi.org/10.1038/s41598-018-35806-5 |
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author | Bianchetti, E. Bates, S. J. Carroll, S. L. Siegelin, M. D. Roth, K. A. |
author_facet | Bianchetti, E. Bates, S. J. Carroll, S. L. Siegelin, M. D. Roth, K. A. |
author_sort | Bianchetti, E. |
collection | PubMed |
description | Malignant peripheral nerve sheath tumors (MPNSTs) are the leading cause of death in neurofibromatosis type 1 (NF1) patients. Current treatment modalities have been largely unsuccessful in improving MPNST patient survival, making the identification of new therapeutic targets urgent. In this study, we found that interference with Usp9X, a deubiquitinating enzyme which is overexpressed in nervous system tumors, or Mcl-1, an anti-apoptotic member of the Bcl-2 family whose degradation is regulated by Usp9X, causes rapid death in human MPNST cell lines. Although both Usp9X and Mcl-1 knockdown elicited some features of apoptosis, broad spectrum caspase inhibition was ineffective in preventing knockdown-induced MPNST cell death suggesting that caspase-independent death pathways were also activated. Ultrastructural examination of MPNST cells following either Usp9X interference or pharmacological inhibition showed extensive cytoplasmic vacuolization and swelling of endoplasmic reticulum (ER) and mitochondria most consistent with paraptotic cell death. Finally, the Usp9X pharmacological inhibitor WP1130 significantly reduced human MPNST growth and induced tumor cell death in an in vivo xenograft model. In total, these findings indicate that Usp9X and Mcl-1 play significant roles in maintaining human MPNST cell viability and that pharmacological inhibition of Usp9X deubiquitinase activity could be a therapeutic target for MPNST treatment. |
format | Online Article Text |
id | pubmed-6255814 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62558142018-12-03 Usp9X Regulates Cell Death in Malignant Peripheral Nerve Sheath Tumors Bianchetti, E. Bates, S. J. Carroll, S. L. Siegelin, M. D. Roth, K. A. Sci Rep Article Malignant peripheral nerve sheath tumors (MPNSTs) are the leading cause of death in neurofibromatosis type 1 (NF1) patients. Current treatment modalities have been largely unsuccessful in improving MPNST patient survival, making the identification of new therapeutic targets urgent. In this study, we found that interference with Usp9X, a deubiquitinating enzyme which is overexpressed in nervous system tumors, or Mcl-1, an anti-apoptotic member of the Bcl-2 family whose degradation is regulated by Usp9X, causes rapid death in human MPNST cell lines. Although both Usp9X and Mcl-1 knockdown elicited some features of apoptosis, broad spectrum caspase inhibition was ineffective in preventing knockdown-induced MPNST cell death suggesting that caspase-independent death pathways were also activated. Ultrastructural examination of MPNST cells following either Usp9X interference or pharmacological inhibition showed extensive cytoplasmic vacuolization and swelling of endoplasmic reticulum (ER) and mitochondria most consistent with paraptotic cell death. Finally, the Usp9X pharmacological inhibitor WP1130 significantly reduced human MPNST growth and induced tumor cell death in an in vivo xenograft model. In total, these findings indicate that Usp9X and Mcl-1 play significant roles in maintaining human MPNST cell viability and that pharmacological inhibition of Usp9X deubiquitinase activity could be a therapeutic target for MPNST treatment. Nature Publishing Group UK 2018-11-26 /pmc/articles/PMC6255814/ /pubmed/30478285 http://dx.doi.org/10.1038/s41598-018-35806-5 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Bianchetti, E. Bates, S. J. Carroll, S. L. Siegelin, M. D. Roth, K. A. Usp9X Regulates Cell Death in Malignant Peripheral Nerve Sheath Tumors |
title | Usp9X Regulates Cell Death in Malignant Peripheral Nerve Sheath Tumors |
title_full | Usp9X Regulates Cell Death in Malignant Peripheral Nerve Sheath Tumors |
title_fullStr | Usp9X Regulates Cell Death in Malignant Peripheral Nerve Sheath Tumors |
title_full_unstemmed | Usp9X Regulates Cell Death in Malignant Peripheral Nerve Sheath Tumors |
title_short | Usp9X Regulates Cell Death in Malignant Peripheral Nerve Sheath Tumors |
title_sort | usp9x regulates cell death in malignant peripheral nerve sheath tumors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6255814/ https://www.ncbi.nlm.nih.gov/pubmed/30478285 http://dx.doi.org/10.1038/s41598-018-35806-5 |
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