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Bortezomib promotes KHSV and EBV lytic cycle by activating JNK and autophagy
- Source :
- Scientific Reports, Scientific Reports, Vol 7, Iss 1, Pp 1-9 (2017)
- Publication Year :
- 2017
- Publisher :
- Springer Science and Business Media LLC, 2017.
-
Abstract
- 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.
- Subjects :
- Gene Expression Regulation, Viral
0301 basic medicine
Herpesvirus 4, Human
Lymphoma, B-Cell
viruses
lcsh:Medicine
Antineoplastic Agents
Virus Replication
Article
Cell Line
Bortezomib
03 medical and health sciences
Gammaherpesvirinae
hemic and lymphatic diseases
Autophagy
medicine
Humans
Cytotoxic T cell
lcsh:Science
Multidisciplinary
business.industry
lcsh:R
medicine.disease
Lymphoma
030104 developmental biology
Lytic cycle
Viral replication
Herpesvirus 8, Human
Cancer cell
Proteasome inhibitor
Cancer research
lcsh:Q
Virus Activation
business
medicine.drug
Subjects
Details
- ISSN :
- 20452322
- Volume :
- 7
- Database :
- OpenAIRE
- Journal :
- Scientific Reports
- Accession number :
- edsair.doi.dedup.....7e3f3acb521f709397afba794df9e991
- Full Text :
- https://doi.org/10.1038/s41598-017-13533-7