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Bortezomib promotes KHSV and EBV lytic cycle by activating JNK and autophagy
KSHV and EBV are gammaherpesviruses strictly linked to human cancers. Even if the majority of cancer cells harbor a latent infection, the few cells that undergo viral replication may contribute to the pathogenesis and maintenance of the virus-associated malignancies. Cytotoxic drugs used for the the...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5638868/ https://www.ncbi.nlm.nih.gov/pubmed/29026157 http://dx.doi.org/10.1038/s41598-017-13533-7 |
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author | Granato, Marisa Romeo, Maria Anele Tiano, Mariangela Sara Santarelli, Roberta Gonnella, Roberta Gilardini Montani, Maria Saveria Faggioni, Alberto Cirone, Mara |
author_facet | Granato, Marisa Romeo, Maria Anele Tiano, Mariangela Sara Santarelli, Roberta Gonnella, Roberta Gilardini Montani, Maria Saveria Faggioni, Alberto Cirone, Mara |
author_sort | Granato, Marisa |
collection | PubMed |
description | KSHV and EBV are gammaherpesviruses strictly linked to human cancers. Even if the majority of cancer cells harbor a latent infection, the few cells that undergo viral replication may contribute to the pathogenesis and maintenance of the virus-associated malignancies. Cytotoxic drugs used for the therapies of cancers harboring virus-infection often have, as side effect, the activation of viral lytic cycle. Therefore it is important to investigate whether they affect viral reactivation and understand the underlying mechanisms involved. In this study, we found that proteasome inhibitor bortezomib, a cytotoxic drug that efficiently target gammaherpesvirus-associated B cell lymphomas, triggered KSHV or EBV viral lytic cycle by activating JNK, in the course of ER stress, and inducing autophagy. These results suggest that the manipulation of these pathways could limit viral spread and improve the outcome of bortezomib treatment in patients affected by gammaherpesvirus-associated lymphomas. |
format | Online Article Text |
id | pubmed-5638868 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56388682017-10-18 Bortezomib promotes KHSV and EBV lytic cycle by activating JNK and autophagy Granato, Marisa Romeo, Maria Anele Tiano, Mariangela Sara Santarelli, Roberta Gonnella, Roberta Gilardini Montani, Maria Saveria Faggioni, Alberto Cirone, Mara Sci Rep Article KSHV and EBV are gammaherpesviruses strictly linked to human cancers. Even if the majority of cancer cells harbor a latent infection, the few cells that undergo viral replication may contribute to the pathogenesis and maintenance of the virus-associated malignancies. Cytotoxic drugs used for the therapies of cancers harboring virus-infection often have, as side effect, the activation of viral lytic cycle. Therefore it is important to investigate whether they affect viral reactivation and understand the underlying mechanisms involved. In this study, we found that proteasome inhibitor bortezomib, a cytotoxic drug that efficiently target gammaherpesvirus-associated B cell lymphomas, triggered KSHV or EBV viral lytic cycle by activating JNK, in the course of ER stress, and inducing autophagy. These results suggest that the manipulation of these pathways could limit viral spread and improve the outcome of bortezomib treatment in patients affected by gammaherpesvirus-associated lymphomas. Nature Publishing Group UK 2017-10-12 /pmc/articles/PMC5638868/ /pubmed/29026157 http://dx.doi.org/10.1038/s41598-017-13533-7 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 Granato, Marisa Romeo, Maria Anele Tiano, Mariangela Sara Santarelli, Roberta Gonnella, Roberta Gilardini Montani, Maria Saveria Faggioni, Alberto Cirone, Mara Bortezomib promotes KHSV and EBV lytic cycle by activating JNK and autophagy |
title | Bortezomib promotes KHSV and EBV lytic cycle by activating JNK and autophagy |
title_full | Bortezomib promotes KHSV and EBV lytic cycle by activating JNK and autophagy |
title_fullStr | Bortezomib promotes KHSV and EBV lytic cycle by activating JNK and autophagy |
title_full_unstemmed | Bortezomib promotes KHSV and EBV lytic cycle by activating JNK and autophagy |
title_short | Bortezomib promotes KHSV and EBV lytic cycle by activating JNK and autophagy |
title_sort | bortezomib promotes khsv and ebv lytic cycle by activating jnk and autophagy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5638868/ https://www.ncbi.nlm.nih.gov/pubmed/29026157 http://dx.doi.org/10.1038/s41598-017-13533-7 |
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