| Literature DB >> 30586159 |
Kazuma Sekiba1, Motoyuki Otsuka1, Motoko Ohno1, Mari Yamagami1, Takahiro Kishikawa1, Takahiro Seimiya1, Tatsunori Suzuki1, Eri Tanaka1, Rei Ishibashi1, Kazuyoshi Funato1, Kazuhiko Koike1.
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.Entities:
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Year: 2019 PMID: 30586159 DOI: 10.1002/hep.30491
Source DB: PubMed Journal: Hepatology ISSN: 0270-9139 Impact factor: 17.425