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Topotecan is a potent inhibitor of SUMOylation in glioblastoma multiforme and alters both cellular replication and metabolic programming
Protein SUMOylation is a dynamic post-translational modification shown to be involved in a diverse set of physiologic processes throughout the cell. SUMOylation has also been shown to play a role in the pathobiology of myriad cancers, one of which is glioblastoma multiforme (GBM). As such, the clini...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5547153/ https://www.ncbi.nlm.nih.gov/pubmed/28785061 http://dx.doi.org/10.1038/s41598-017-07631-9 |
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author | Bernstock, Joshua D. Ye, Daniel Gessler, Florian A. Lee, Yang-ja Peruzzotti-Jametti, Luca Baumgarten, Peter Johnson, Kory R. Maric, Dragan Yang, Wei Kögel, Donat Pluchino, Stefano Hallenbeck, John M. |
author_facet | Bernstock, Joshua D. Ye, Daniel Gessler, Florian A. Lee, Yang-ja Peruzzotti-Jametti, Luca Baumgarten, Peter Johnson, Kory R. Maric, Dragan Yang, Wei Kögel, Donat Pluchino, Stefano Hallenbeck, John M. |
author_sort | Bernstock, Joshua D. |
collection | PubMed |
description | Protein SUMOylation is a dynamic post-translational modification shown to be involved in a diverse set of physiologic processes throughout the cell. SUMOylation has also been shown to play a role in the pathobiology of myriad cancers, one of which is glioblastoma multiforme (GBM). As such, the clinical significance and therapeutic utility offered via the selective control of global SUMOylation is readily apparent. There are, however, relatively few known/effective inhibitors of global SUMO-conjugation. Herein we describe the identification of topotecan as a novel inhibitor of global SUMOylation. We also provide evidence that inhibition of SUMOylation by topotecan is associated with reduced levels of CDK6 and HIF-1α, as well as pronounced changes in cell cycle progression and cellular metabolism, thereby highlighting its putative role as an adjuvant therapy in defined GBM patient populations. |
format | Online Article Text |
id | pubmed-5547153 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55471532017-08-09 Topotecan is a potent inhibitor of SUMOylation in glioblastoma multiforme and alters both cellular replication and metabolic programming Bernstock, Joshua D. Ye, Daniel Gessler, Florian A. Lee, Yang-ja Peruzzotti-Jametti, Luca Baumgarten, Peter Johnson, Kory R. Maric, Dragan Yang, Wei Kögel, Donat Pluchino, Stefano Hallenbeck, John M. Sci Rep Article Protein SUMOylation is a dynamic post-translational modification shown to be involved in a diverse set of physiologic processes throughout the cell. SUMOylation has also been shown to play a role in the pathobiology of myriad cancers, one of which is glioblastoma multiforme (GBM). As such, the clinical significance and therapeutic utility offered via the selective control of global SUMOylation is readily apparent. There are, however, relatively few known/effective inhibitors of global SUMO-conjugation. Herein we describe the identification of topotecan as a novel inhibitor of global SUMOylation. We also provide evidence that inhibition of SUMOylation by topotecan is associated with reduced levels of CDK6 and HIF-1α, as well as pronounced changes in cell cycle progression and cellular metabolism, thereby highlighting its putative role as an adjuvant therapy in defined GBM patient populations. Nature Publishing Group UK 2017-08-07 /pmc/articles/PMC5547153/ /pubmed/28785061 http://dx.doi.org/10.1038/s41598-017-07631-9 Text en © The Author(s) 2017 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 Bernstock, Joshua D. Ye, Daniel Gessler, Florian A. Lee, Yang-ja Peruzzotti-Jametti, Luca Baumgarten, Peter Johnson, Kory R. Maric, Dragan Yang, Wei Kögel, Donat Pluchino, Stefano Hallenbeck, John M. Topotecan is a potent inhibitor of SUMOylation in glioblastoma multiforme and alters both cellular replication and metabolic programming |
title | Topotecan is a potent inhibitor of SUMOylation in glioblastoma multiforme and alters both cellular replication and metabolic programming |
title_full | Topotecan is a potent inhibitor of SUMOylation in glioblastoma multiforme and alters both cellular replication and metabolic programming |
title_fullStr | Topotecan is a potent inhibitor of SUMOylation in glioblastoma multiforme and alters both cellular replication and metabolic programming |
title_full_unstemmed | Topotecan is a potent inhibitor of SUMOylation in glioblastoma multiforme and alters both cellular replication and metabolic programming |
title_short | Topotecan is a potent inhibitor of SUMOylation in glioblastoma multiforme and alters both cellular replication and metabolic programming |
title_sort | topotecan is a potent inhibitor of sumoylation in glioblastoma multiforme and alters both cellular replication and metabolic programming |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5547153/ https://www.ncbi.nlm.nih.gov/pubmed/28785061 http://dx.doi.org/10.1038/s41598-017-07631-9 |
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