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dc.creatorLundstrom, Kenneth
dc.creatorHromić-Jahjefendić, Altijana
dc.creatorBilajac, Esma
dc.creatorAljabali, Alaa
dc.creatorBaralić, Katarina
dc.creatorSabri, Nagwa
dc.creatorShehata, Eslam
dc.creatorRaslan, Mohamed
dc.creatorRaslan, Sara
dc.creatorFerreira, Ana Cl ́audia
dc.creatorOrlandi, Lidiane
dc.creatorSerrano-Aroca, Angel
dc.creatorUversky, Vladimir
dc.creatorHassan, Sk. Sarif
dc.creatorRedwan, Elrashdy
dc.creatorAzevedo, Vasco
dc.creatorAlzahrani, Khalid
dc.creatorAlsharif, Khalaf
dc.creatorHalawani, Ibrahim
dc.creatorAlzahrani, Fuad
dc.creatorTambuwala, Murtaza
dc.creatorBarh, Debmalya
dc.date.accessioned2023-01-09T09:23:16Z
dc.date.available2023-01-09T09:23:16Z
dc.date.issued2023
dc.identifier.issn0898-6568
dc.identifier.urihttps://farfar.pharmacy.bg.ac.rs/handle/123456789/4365
dc.description.abstractThe COVID-19 pandemic has triggered intensive research and development of drugs and vaccines against SARS-CoV-2 during the last two years. The major success was especially observed with development of vaccines based on viral vectors, nucleic acids and whole viral particles, which have received emergent authorization leading to global mass vaccinations. Although the vaccine programs have made a big impact on COVID-19 spread and severity, emerging novel variants have raised serious concerns about vaccine efficacy. Due to the urgent demand, drug development had originally to rely on repurposing of antiviral drugs developed against other infectious diseases. For both drug and vaccine development the focus has been mainly on SARS-CoV-2 surface proteins and host cell receptors involved in viral attachment and entry. In this review, we expand the spectrum of SARS-CoV-2 targets by investigating the COVID-19 signalome. In addition to the SARS-CoV-2 Spike protein, the envelope, membrane, and nucleoprotein targets have been subjected to research. Moreover, viral proteases have presented the possibility to develop different strategies for the inhibition of SARS-CoV-2 replication and spread. Several signaling pathways involving the renin-angiotensin system, angiotensin-converting enzymes, immune pathways, hypoxia, and calcium signaling have provided attractive alternative targets for more efficient drug development.
dc.publisherElsevier Inc.
dc.rightsrestrictedAccess
dc.sourceCellular Signalling
dc.subjectCOVID-19
dc.subjectSARS-CoV-2
dc.subjectAntiviral drugs
dc.subjectSignaling pathways
dc.subjectSignalome
dc.subjectVaccines
dc.titleCOVID-19 signalome: Potential therapeutic interventions
dc.typearticle
dc.rights.licenseARR
dc.citation.volume103
dc.citation.rankM22~
dc.identifier.wos000917070200001
dc.identifier.doi10.1016/j.cellsig.2022.110559
dc.identifier.pmid36521656
dc.identifier.scopus2-s2.0-85144807510
dc.type.versionpublishedVersion


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