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KIF11 inhibition decreases cytopathogenesis and replication of influenza A virusopen access

Authors
Kim, Dong-InKang, Ji-HunKim, Eui-HoSeo, Young-Jin
Issue Date
Apr-2021
Publisher
KOREAN SOCIETY TOXICOGENOMICS & TOXICOPROTEOMICS-KSTT
Keywords
KIF11; Influenza A virus; Viral cytopathogenesis; Anti-viral drug
Citation
MOLECULAR & CELLULAR TOXICOLOGY, v.17, no.2, pp 201 - 212
Pages
12
Journal Title
MOLECULAR & CELLULAR TOXICOLOGY
Volume
17
Number
2
Start Page
201
End Page
212
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/48079
DOI
10.1007/s13273-021-00126-9
ISSN
1738-642X
2092-8467
Abstract
Background Seasonal flu is an infectious disease of the respiratory tract caused by influenza viruses. The development of anti-influenza drugs has significantly reduced the threat from the influenza virus; however, frequent mutations of this negative RNA virus result in antiviral-resistant strains, and constantly intimidate the human race. Thus, identifying novel therapeutic targets for the prevention and treatment of influenza virus infections is critical. Objective We aimed to determine whether the kinesin superfamily protein 11 (KIF11) inhibitors, monastrol and K858, inhibit viral cytopathogenesis and influenza A virus (IAV) replication. Result When MDCK or HEK293 cells were treated with monastrol and K858 that did not induce significant cytotoxicity, IAV-induced cytopathic effect was attenuated significantly. Furthermore, these inhibitors effectively suppressed the production of viral RNA, proteins, and infectious viral particles. Conclusion Inhibition of KIF11 activity effectively attenuates virus-mediated cytopathic effect and suppresses viral replication. Hence, KIF11 is a potential therapeutic target against the influenza virus.
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Seo, Young Jin
자연과학대학 (생명과학과)
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