Evidence map›Paper›PMID 36992362›Full record

ArticleViruses2023

Inhibitors of the Ubiquitin-Mediated Signaling Pathway Exhibit Broad-Spectrum Antiviral Activities against New World Alphaviruses.

Niloufar A Boghdeh, Brittany McGraw, Michael D Barrera, Carol Anderson, Haseebullah Baha, Kenneth H Risner, Ifedayo V Ogungbe, Farhang Alem, Aarthi Narayanan

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.9field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 10 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Niloufar A BoghdehBiomedical Research Laboratory, George Mason University, Manassas, VA 20110, USA.ORCID 0000-0002-2678-6481
Brittany McGrawSchool of Systems Biology, College of Science, George Mason University, Manassas, VA 20110, USA.
Michael D BarreraBiomedical Research Laboratory, George Mason University, Manassas, VA 20110, USA.
Carol AndersonBiomedical Research Laboratory, George Mason University, Manassas, VA 20110, USA.
Haseebullah BahaBiomedical Research Laboratory, George Mason University, Manassas, VA 20110, USA.
Kenneth H RisnerBiomedical Research Laboratory, George Mason University, Manassas, VA 20110, USA.
Ifedayo V OgungbeDepartment of Chemistry, Physics and Atmospheric Sciences, Jackson State University, Jackson, MS 39217, USA.ORCID 0000-0002-8048-5137
Farhang AlemBiomedical Research Laboratory, George Mason University, Manassas, VA 20110, USA.ORCID 0000-0002-4288-2502
Aarthi NarayananBiomedical Research Laboratory, George Mason University, Manassas, VA 20110, USA.
George Mason University · USJackson State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

New World alphaviruses including Venezuelan Equine Encephalitis Virus (VEEV) and Eastern Equine Encephalitis Virus (EEEV) are mosquito-transmitted viruses that cause disease in humans and equines. There are currently no FDA-approved therapeutics or vaccines to treat or prevent exposure-associated encephalitic disease. The ubiquitin proteasome system (UPS)-associated signaling events are known to play an important role in the establishment of a productive infection for several acutely infectious viruses. The critical engagement of the UPS-associated signaling mechanisms by many viruses as host-pathogen interaction hubs led us to hypothesize that small molecule inhibitors that interfere with these signaling pathways will exert broad-spectrum inhibitory activity against alphaviruses. We queried eight inhibitors of the UPS signaling pathway for antiviral outcomes against VEEV. Three of the tested inhibitors, namely NSC697923 (NSC), bardoxolone methyl (BARM) and omaveloxolone (OMA) demonstrated broad-spectrum antiviral activity against VEEV and EEEV. Dose dependency and time of addition studies suggest that BARM and OMA exhibit intracellular and post-entry viral inhibition. Cumulatively, our studies indicate that inhibitors of the UPS-associated signaling pathways exert broad-spectrum antiviral outcomes in the context of VEEV and EEEV infection, supporting their translational application as therapeutic candidates to treat alphavirus infections.

Indexed as

AlphavirusEncephalitis Virus, Venezuelan EquineAnimalsAntiviral AgentsHorsesHumansSignal TransductionUbiquitinAntiviral AgentsUbiquitinalphavirusantiinflammatoryantiviralbardoxolone methylEastern Equine Encephalitis Virusomaveloxolonetherapeuticsubiquitin proteasome systemubiquitin signaling pathwaysVenezuelan Equine Encephalitis Virus

Identifiers

PMID36992362
PMCPMC10059822
OpenAlexW4322742215

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.