Publication:
Re-analysis of SARS-CoV-2-infected host cell proteomics time-course data by impact pathway analysis and network analysis: a potential link with inflammatory response.

dc.contributor.authorBock, Jens-Ole
dc.contributor.authorOrtea, Ignacio
dc.contributor.funderMiguel Servet Programme
dc.contributor.funderInstituto de Salud Carlos III
dc.contributor.funderEuropean Social Fund
dc.date.accessioned2023-02-09T09:35:59Z
dc.date.available2023-02-09T09:35:59Z
dc.date.issued2020-05-30
dc.description.abstractCoronavirus disease 2019 (COVID-19), caused by an outbreak of the severe acute respiratory syndrome-coronavirus 2 (SARS-CoV-2) in Wuhan, China, has led to an unprecedented health and economic crisis worldwide. To develop treatments that can stop or lessen the symptoms and severity of SARS-CoV-2 infection, it is critical to understand how the virus behaves inside human cells, and so far studies in this area remain scarce. A recent study investigated translatome and proteome host cell changes induced in vitro by SARS-CoV-2. Here, we use the publicly available proteomics data from this study to re-analyze the in vitro cellular consequences of SARS-CoV-2 infection by impact pathways analysis and network analysis. Notably, proteins linked to the inflammatory response, but also proteins related to chromosome segregation during mitosis, were found to be altered in response to viral infection. Upregulation of inflammatory response proteins is in line with the propagation of inflammatory reaction and lung injury that is observed in advanced stages of COVID-19 patients and which worsens with age.
dc.description.versionSi
dc.identifier.citationBock JO, Ortea I. Re-analysis of SARS-CoV-2-infected host cell proteomics time-course data by impact pathway analysis and network analysis: a potential link with inflammatory response. Aging (Albany NY). 2020 Jun 23;12(12):11277-11286
dc.identifier.doi10.18632/aging.103524
dc.identifier.essn1945-4589
dc.identifier.pmcPMC7343490
dc.identifier.pmid32575076
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7343490/pdf
dc.identifier.unpaywallURLhttps://www.aging-us.com/article/103524/pdf
dc.identifier.urihttp://hdl.handle.net/10668/15804
dc.issue.number12
dc.journal.titleAging
dc.journal.titleabbreviationAging (Albany NY)
dc.language.isoen
dc.organizationInstituto de Investigación e Innovación en Ciencias Biomédicas
dc.page.number11277-11286
dc.provenanceRealizada la curación de contenido 28/08/2024
dc.publisherImpact Journals LLC
dc.pubmedtypeJournal Article
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.relation.projectIDCP19/00164
dc.relation.publisherversionhttps://www.aging-us.com/article/103524/text
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectCOVID-19
dc.subjectSARS-CoV-2
dc.subjectInflammatory response
dc.subjectProteomics
dc.subject.decsEnvejecimiento
dc.subject.decsEnzima convertidora de angiotensina 2
dc.subject.decsInfecciones por Coronavirus
dc.subject.decsInflamación
dc.subject.decsNeumonía viral
dc.subject.decsPandemias
dc.subject.decsRedes reguladoras de genes
dc.subject.decsReplicación viral
dc.subject.meshAging
dc.subject.meshAngiotensin-converting enzyme 2
dc.subject.meshBetacoronavirus
dc.subject.meshCOVID-19
dc.subject.meshCoronavirus infections
dc.subject.meshGene expression regulation
dc.subject.meshGene regulatory networks
dc.subject.meshHumans
dc.subject.meshInflammation
dc.subject.meshPandemics
dc.subject.meshPeptidyl-dipeptidase A
dc.subject.meshPneumonia, viral
dc.subject.meshProteomics
dc.subject.meshSARS-CoV-2
dc.subject.meshVirus replication
dc.titleRe-analysis of SARS-CoV-2-infected host cell proteomics time-course data by impact pathway analysis and network analysis: a potential link with inflammatory response.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number12
dspace.entity.typePublication

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