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Using glycyrrhizic acid to target sumoylation processes during Epstein-Barr virus latency

Cellular sumoylation processes are proposed targets for anti-viral and anti-cancer therapies. We reported that Epstein-Barr virus (EBV) latent membrane protein 1 (LMP1) dysregulates cellular sumoylation processes, contributing to its oncogenic potential in EBV-associated malignancies. Ginkgolic acid...

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Autores principales: Bentz, Gretchen L., Lowrey, Angela J., Horne, Dustin C., Nguyen, Vy, Satterfield, Austin R., Ross, Tabithia D., Harrod, Abigail E., Uchakina, Olga N., McKallip, Robert J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6534330/
https://www.ncbi.nlm.nih.gov/pubmed/31125383
http://dx.doi.org/10.1371/journal.pone.0217578
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author Bentz, Gretchen L.
Lowrey, Angela J.
Horne, Dustin C.
Nguyen, Vy
Satterfield, Austin R.
Ross, Tabithia D.
Harrod, Abigail E.
Uchakina, Olga N.
McKallip, Robert J.
author_facet Bentz, Gretchen L.
Lowrey, Angela J.
Horne, Dustin C.
Nguyen, Vy
Satterfield, Austin R.
Ross, Tabithia D.
Harrod, Abigail E.
Uchakina, Olga N.
McKallip, Robert J.
author_sort Bentz, Gretchen L.
collection PubMed
description Cellular sumoylation processes are proposed targets for anti-viral and anti-cancer therapies. We reported that Epstein-Barr virus (EBV) latent membrane protein 1 (LMP1) dysregulates cellular sumoylation processes, contributing to its oncogenic potential in EBV-associated malignancies. Ginkgolic acid and anacardic acid, known inhibitors of sumoylation, inhibit LMP1-induced protein sumoylation; however, both drugs have adverse effects in hosts. Here we test the effects of glycyrrhizic acid, a medicinal botanical extract with anti-inflammatory, anti-carcinogenic, and anti-viral properties, on cellular sumoylation processes. While glycyrrhizic acid is known to inhibit EBV penetration, its affect on cellular sumoylation processes remains to be documented. We hypothesized that glycyrrhizic acid inhibits cellular sumoylation processes and may be a viable treatment for Epstein-Barr virus-associated malignancies. Results showed that glycyrrhizic acid inhibited sumoylation processes (without affecting ubiquitination processes), limited cell growth, and induced apoptosis in multiple cell lines. Similar to ginkgolic acid; glycyrrhizic acid targeted the first step of the sumoylation process and resulted in low levels of spontaneous EBV reactivation. Glycyrrhizic acid did not affect induced reactivation of the virus, but the presence of the extract did reduce the ability of the produced virus to infect additional cells. Therefore, we propose that glycyrrhizic acid may be a potential therapeutic drug to augment the treatment of EBV-associated lymphoid malignancies.
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spelling pubmed-65343302019-06-05 Using glycyrrhizic acid to target sumoylation processes during Epstein-Barr virus latency Bentz, Gretchen L. Lowrey, Angela J. Horne, Dustin C. Nguyen, Vy Satterfield, Austin R. Ross, Tabithia D. Harrod, Abigail E. Uchakina, Olga N. McKallip, Robert J. PLoS One Research Article Cellular sumoylation processes are proposed targets for anti-viral and anti-cancer therapies. We reported that Epstein-Barr virus (EBV) latent membrane protein 1 (LMP1) dysregulates cellular sumoylation processes, contributing to its oncogenic potential in EBV-associated malignancies. Ginkgolic acid and anacardic acid, known inhibitors of sumoylation, inhibit LMP1-induced protein sumoylation; however, both drugs have adverse effects in hosts. Here we test the effects of glycyrrhizic acid, a medicinal botanical extract with anti-inflammatory, anti-carcinogenic, and anti-viral properties, on cellular sumoylation processes. While glycyrrhizic acid is known to inhibit EBV penetration, its affect on cellular sumoylation processes remains to be documented. We hypothesized that glycyrrhizic acid inhibits cellular sumoylation processes and may be a viable treatment for Epstein-Barr virus-associated malignancies. Results showed that glycyrrhizic acid inhibited sumoylation processes (without affecting ubiquitination processes), limited cell growth, and induced apoptosis in multiple cell lines. Similar to ginkgolic acid; glycyrrhizic acid targeted the first step of the sumoylation process and resulted in low levels of spontaneous EBV reactivation. Glycyrrhizic acid did not affect induced reactivation of the virus, but the presence of the extract did reduce the ability of the produced virus to infect additional cells. Therefore, we propose that glycyrrhizic acid may be a potential therapeutic drug to augment the treatment of EBV-associated lymphoid malignancies. Public Library of Science 2019-05-24 /pmc/articles/PMC6534330/ /pubmed/31125383 http://dx.doi.org/10.1371/journal.pone.0217578 Text en © 2019 Bentz et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Bentz, Gretchen L.
Lowrey, Angela J.
Horne, Dustin C.
Nguyen, Vy
Satterfield, Austin R.
Ross, Tabithia D.
Harrod, Abigail E.
Uchakina, Olga N.
McKallip, Robert J.
Using glycyrrhizic acid to target sumoylation processes during Epstein-Barr virus latency
title Using glycyrrhizic acid to target sumoylation processes during Epstein-Barr virus latency
title_full Using glycyrrhizic acid to target sumoylation processes during Epstein-Barr virus latency
title_fullStr Using glycyrrhizic acid to target sumoylation processes during Epstein-Barr virus latency
title_full_unstemmed Using glycyrrhizic acid to target sumoylation processes during Epstein-Barr virus latency
title_short Using glycyrrhizic acid to target sumoylation processes during Epstein-Barr virus latency
title_sort using glycyrrhizic acid to target sumoylation processes during epstein-barr virus latency
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6534330/
https://www.ncbi.nlm.nih.gov/pubmed/31125383
http://dx.doi.org/10.1371/journal.pone.0217578
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