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Pevonedistat, a Neuronal Precursor Cell-Expressed Developmentally Down-Regulated Protein 8-Activating Enzyme Inhibitor, Is a Potent Inhibitor of Hepatitis B Virus.

Authors :
Sekiba K
Otsuka M
Ohno M
Yamagami M
Kishikawa T
Seimiya T
Suzuki T
Tanaka E
Ishibashi R
Funato K
Koike K
Source :
Hepatology (Baltimore, Md.) [Hepatology] 2019 May; Vol. 69 (5), pp. 1903-1915. Date of Electronic Publication: 2019 Mar 13.
Publication Year :
2019

Abstract

Hepatitis B virus (HBV) infection is a major health concern worldwide. To prevent HBV-related mortality, elimination of viral proteins is considered the ultimate goal of HBV treatment; however, currently available nucleos(t)ide analogs rarely achieve this goal, as viral transcription from episomal viral covalently closed circular DNA (cccDNA) is not prevented. HBV regulatory protein X was recently found to target the protein structural maintenance of chromosomes 5/6 (Smc5/6) for ubiquitination and degradation by DDB1-CUL4-ROC1 E3 ligase, resulting in enhanced viral transcription from cccDNA. This ubiquitin-dependent proteasomal pathway requires an additional ubiquitin-like protein for activation, neuronal precursor cell-expressed developmentally down-regulated protein 8 (NEDD8). Here, we show that pevonedistat, a NEDD8-activating enzyme inhibitor, works efficiently as an antiviral agent. Pevonedistat significantly restored Smc5/6 protein levels and suppressed viral transcription and protein production in the HBV minicircle system in in vitro HBV replication models and in human primary hepatocytes infected naturally with HBV. Conclusion: These results indicate that pevonedistat is a promising compound to treat chronic HBV infection.<br /> (© 2018 by the American Association for the Study of Liver Diseases.)

Details

Language :
English
ISSN :
1527-3350
Volume :
69
Issue :
5
Database :
MEDLINE
Journal :
Hepatology (Baltimore, Md.)
Publication Type :
Academic Journal
Accession number :
30586159
Full Text :
https://doi.org/10.1002/hep.30491