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Positioning SUMO as an immunological facilitator of oncolytic viruses for high-grade glioma
Oncolytic viral (OV) therapies are promising novel treatment modalities for cancers refractory to conventional treatment, such as glioblastoma, within the central nervous system (CNS). Although OVs have received regulatory approval for use in the CNS, efficacy is hampered by obstacles related to del...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10582965/ https://www.ncbi.nlm.nih.gov/pubmed/37860820 http://dx.doi.org/10.3389/fcell.2023.1271575 |
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author | Karandikar, Paramesh V. Suh, Lyle Gerstl, Jakob V. E. Blitz, Sarah E. Qu, Qing Rui Won, Sae-Yeon Gessler, Florian A. Arnaout, Omar Smith, Timothy R. Peruzzi, Pier Paolo Yang, Wei Friedman, Gregory K. Bernstock, Joshua D. |
author_facet | Karandikar, Paramesh V. Suh, Lyle Gerstl, Jakob V. E. Blitz, Sarah E. Qu, Qing Rui Won, Sae-Yeon Gessler, Florian A. Arnaout, Omar Smith, Timothy R. Peruzzi, Pier Paolo Yang, Wei Friedman, Gregory K. Bernstock, Joshua D. |
author_sort | Karandikar, Paramesh V. |
collection | PubMed |
description | Oncolytic viral (OV) therapies are promising novel treatment modalities for cancers refractory to conventional treatment, such as glioblastoma, within the central nervous system (CNS). Although OVs have received regulatory approval for use in the CNS, efficacy is hampered by obstacles related to delivery, under-/over-active immune responses, and the “immune-cold” nature of most CNS malignancies. SUMO, the Small Ubiquitin-like Modifier, is a family of proteins that serve as a high-level regulator of a large variety of key physiologic processes including the host immune response. The SUMO pathway has also been implicated in the pathogenesis of both wild-type viruses and CNS malignancies. As such, the intersection of OV biology with the SUMO pathway makes SUMOtherapeutics particularly interesting as adjuvant therapies for the enhancement of OV efficacy alone and in concert with other immunotherapeutic agents. Accordingly, the authors herein provide: 1) an overview of the SUMO pathway and its role in CNS malignancies; 2) describe the current state of CNS-targeted OVs; and 3) describe the interplay between the SUMO pathway and the viral lifecycle and host immune response. |
format | Online Article Text |
id | pubmed-10582965 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-105829652023-10-19 Positioning SUMO as an immunological facilitator of oncolytic viruses for high-grade glioma Karandikar, Paramesh V. Suh, Lyle Gerstl, Jakob V. E. Blitz, Sarah E. Qu, Qing Rui Won, Sae-Yeon Gessler, Florian A. Arnaout, Omar Smith, Timothy R. Peruzzi, Pier Paolo Yang, Wei Friedman, Gregory K. Bernstock, Joshua D. Front Cell Dev Biol Cell and Developmental Biology Oncolytic viral (OV) therapies are promising novel treatment modalities for cancers refractory to conventional treatment, such as glioblastoma, within the central nervous system (CNS). Although OVs have received regulatory approval for use in the CNS, efficacy is hampered by obstacles related to delivery, under-/over-active immune responses, and the “immune-cold” nature of most CNS malignancies. SUMO, the Small Ubiquitin-like Modifier, is a family of proteins that serve as a high-level regulator of a large variety of key physiologic processes including the host immune response. The SUMO pathway has also been implicated in the pathogenesis of both wild-type viruses and CNS malignancies. As such, the intersection of OV biology with the SUMO pathway makes SUMOtherapeutics particularly interesting as adjuvant therapies for the enhancement of OV efficacy alone and in concert with other immunotherapeutic agents. Accordingly, the authors herein provide: 1) an overview of the SUMO pathway and its role in CNS malignancies; 2) describe the current state of CNS-targeted OVs; and 3) describe the interplay between the SUMO pathway and the viral lifecycle and host immune response. Frontiers Media S.A. 2023-10-04 /pmc/articles/PMC10582965/ /pubmed/37860820 http://dx.doi.org/10.3389/fcell.2023.1271575 Text en Copyright © 2023 Karandikar, Suh, Gerstl, Blitz, Qu, Won, Gessler, Arnaout, Smith, Peruzzi, Yang, Friedman and Bernstock. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Karandikar, Paramesh V. Suh, Lyle Gerstl, Jakob V. E. Blitz, Sarah E. Qu, Qing Rui Won, Sae-Yeon Gessler, Florian A. Arnaout, Omar Smith, Timothy R. Peruzzi, Pier Paolo Yang, Wei Friedman, Gregory K. Bernstock, Joshua D. Positioning SUMO as an immunological facilitator of oncolytic viruses for high-grade glioma |
title | Positioning SUMO as an immunological facilitator of oncolytic viruses for high-grade glioma |
title_full | Positioning SUMO as an immunological facilitator of oncolytic viruses for high-grade glioma |
title_fullStr | Positioning SUMO as an immunological facilitator of oncolytic viruses for high-grade glioma |
title_full_unstemmed | Positioning SUMO as an immunological facilitator of oncolytic viruses for high-grade glioma |
title_short | Positioning SUMO as an immunological facilitator of oncolytic viruses for high-grade glioma |
title_sort | positioning sumo as an immunological facilitator of oncolytic viruses for high-grade glioma |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10582965/ https://www.ncbi.nlm.nih.gov/pubmed/37860820 http://dx.doi.org/10.3389/fcell.2023.1271575 |
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