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Article: Targeting Polyamine Metabolism for Control of Human Viral Diseases

TitleTargeting Polyamine Metabolism for Control of Human Viral Diseases
Authors
Keywordspolyamine metabolism
virus
infection
diseases
Issue Date2020
PublisherDove Medical Press Ltd. The Journal's web site is located at https://www.dovepress.com/infection-and-drug-resistance-journal
Citation
Infection and Drug Resistance, 2020, v. 2020 n. 13, p. 4335-4346 How to Cite?
AbstractA virus is an infectious particle which generally contains nucleic acid genome (DNA or RNA inside a protein shell), except for human immunodeficiency virus (HIV). Viruses have to reproduce by infecting their host cells. Polyamines are ubiquitous compounds in mammalian cells and play key roles in various cellular processes. The metabolic pathways of polyamines have been well studied. Targeting these metabolic pathways can reduce infections caused by viruses. In the study, we systematically reviewed the association of polyamine metabolic pathways and viruses including coxsackievirus B3 (CVB3), enterovirus 71 (EV71), poliovirus (PV), Zika virus (ZKV), hepatitis C virus (HCV), hepatitis B virus (HBV), dengue virus (DENV), Japanese encephalitis virus (JEV), yellow fever virus (YFV), Ebola virus (EBOV), marburgvirus (MARV), chikungunya virus (CHIKV), sindbis virus (SINV), Semliki Forest virus (SFV), Epstein–Barr virus (EBV), herpes simplex virus 1 (HSV), human cytomegalovirus (HCMV), vesicular stomatitis virus (VSV), Rabies virus (RABV), Rift Valley fever virus (RVFV), La Crosse virus (LACV), human immunodeficiency virus (HIV), Middle East respiratory syndrome virus (MERS-CoV), and coronavirus disease 2019 (SARS-CoV-2). This review revealed that targeting polyamine metabolic pathways may be a potential approach to control human viral infection.
Persistent Identifierhttp://hdl.handle.net/10722/295213
ISSN
2021 Impact Factor: 4.177
2020 SCImago Journal Rankings: 1.033
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorHuang, M-
dc.contributor.authorZhang, W-
dc.contributor.authorChen, H-
dc.contributor.authorZeng, J-
dc.date.accessioned2021-01-11T13:56:56Z-
dc.date.available2021-01-11T13:56:56Z-
dc.date.issued2020-
dc.identifier.citationInfection and Drug Resistance, 2020, v. 2020 n. 13, p. 4335-4346-
dc.identifier.issn1178-6973-
dc.identifier.urihttp://hdl.handle.net/10722/295213-
dc.description.abstractA virus is an infectious particle which generally contains nucleic acid genome (DNA or RNA inside a protein shell), except for human immunodeficiency virus (HIV). Viruses have to reproduce by infecting their host cells. Polyamines are ubiquitous compounds in mammalian cells and play key roles in various cellular processes. The metabolic pathways of polyamines have been well studied. Targeting these metabolic pathways can reduce infections caused by viruses. In the study, we systematically reviewed the association of polyamine metabolic pathways and viruses including coxsackievirus B3 (CVB3), enterovirus 71 (EV71), poliovirus (PV), Zika virus (ZKV), hepatitis C virus (HCV), hepatitis B virus (HBV), dengue virus (DENV), Japanese encephalitis virus (JEV), yellow fever virus (YFV), Ebola virus (EBOV), marburgvirus (MARV), chikungunya virus (CHIKV), sindbis virus (SINV), Semliki Forest virus (SFV), Epstein–Barr virus (EBV), herpes simplex virus 1 (HSV), human cytomegalovirus (HCMV), vesicular stomatitis virus (VSV), Rabies virus (RABV), Rift Valley fever virus (RVFV), La Crosse virus (LACV), human immunodeficiency virus (HIV), Middle East respiratory syndrome virus (MERS-CoV), and coronavirus disease 2019 (SARS-CoV-2). This review revealed that targeting polyamine metabolic pathways may be a potential approach to control human viral infection.-
dc.languageeng-
dc.publisherDove Medical Press Ltd. The Journal's web site is located at https://www.dovepress.com/infection-and-drug-resistance-journal-
dc.relation.ispartofInfection and Drug Resistance-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectpolyamine metabolism-
dc.subjectvirus-
dc.subjectinfection-
dc.subjectdiseases-
dc.titleTargeting Polyamine Metabolism for Control of Human Viral Diseases-
dc.typeArticle-
dc.identifier.emailChen, H: haiyong@hku.hk-
dc.identifier.authorityChen, H=rp01923-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.2147/IDR.S262024-
dc.identifier.pmid33293837-
dc.identifier.pmcidPMC7718961-
dc.identifier.scopuseid_2-s2.0-85097824728-
dc.identifier.hkuros320816-
dc.identifier.volume2020-
dc.identifier.issue13-
dc.identifier.spage4335-
dc.identifier.epage4346-
dc.identifier.isiWOS:000597248500002-
dc.publisher.placeUnited Kingdom-

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