Evidence map›Paper›PMID 33946802›Full record

ArticleMolecules (Basel, Switzerland)2021

Antiviral Properties of the NSAID Drug Naproxen Targeting the Nucleoprotein of SARS-CoV-2 Coronavirus.

Olivier Terrier, Sébastien Dilly, Andrés Pizzorno, Dominika Chalupska, Jana Humpolickova, Evžen Bouřa, Francis Berenbaum, Stéphane Quideau, Bruno Lina, Bruno Fève and 6 more

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 7% 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

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 44 citations in OpenAlex.

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  19. Analgesia and COVID-19.British journal of clinical pharmacology · 2022
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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

16 authors at 5 institutions in 2 countries.

Olivier TerrierCIRI, Centre International de Recherche en Infectiologie, (Team VirPath), Univ Lyon, Inserm, U1111, Université Claude Bernard Lyon 1, CNRS, UMR5308, ENS de Lyon, F-69007 Lyon, France.ORCID 0000-0001-9393-7684
Sébastien DillyCancer Biology and Therapeutics Team, INSERM, UMR_S 938, Centre de Recherche Saint-Antoine, Sorbonne Universitè, F-75012 Paris, France.
Andrés PizzornoCIRI, Centre International de Recherche en Infectiologie, (Team VirPath), Univ Lyon, Inserm, U1111, Université Claude Bernard Lyon 1, CNRS, UMR5308, ENS de Lyon, F-69007 Lyon, France.ORCID 0000-0002-0918-6804
Dominika ChalupskaInstitute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, 11720 Prague, Czech Republic.
Jana HumpolickovaInstitute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, 11720 Prague, Czech Republic.
Evžen BouřaInstitute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, 11720 Prague, Czech Republic.
Francis BerenbaumINSERM, UMR_S 938, Centre de Recherche Saint-Antoine, Sorbonne University, and Department of Rheumatology, AP-HP Saint-Antoine Hospital, F-75012 Paris, France.
Stéphane QuideauISM, UMR-CNRS 5255, Université de Bordeaux, F-33405 Talence, France.
Bruno LinaCIRI, Centre International de Recherche en Infectiologie, (Team VirPath), Univ Lyon, Inserm, U1111, Université Claude Bernard Lyon 1, CNRS, UMR5308, ENS de Lyon, F-69007 Lyon, France.ORCID 0000-0002-8959-2123
Bruno FèveGenetic and acquired lipodystrophies Team, INSERM, UMR_S 938, Centre de Recherche Saint-Antoine, Sorbonne Université, F-75012 Paris, France.ORCID 0000-0001-6577-9009
Frédéric AdnetService d'Urgences-SAMU-SMUR, Hôpital Avicenne, AP-HP, F-93000 Bobigny, France.
Michèle SabbahCancer Biology and Therapeutics Team, INSERM, UMR_S 938, Centre de Recherche Saint-Antoine, Sorbonne Universitè, F-75012 Paris, France.ORCID 0000-0001-5368-9022
Manuel Rosa-CalatravaCIRI, Centre International de Recherche en Infectiologie, (Team VirPath), Univ Lyon, Inserm, U1111, Université Claude Bernard Lyon 1, CNRS, UMR5308, ENS de Lyon, F-69007 Lyon, France.
Vincent MaréchalCancer Biology and Therapeutics Team, INSERM, UMR_S 938, Centre de Recherche Saint-Antoine, Sorbonne Universitè, F-75012 Paris, France.
Julien HenriLaboratoire de Biologie Computationnelle et Quantitative, Institut de Biologie Paris-Seine, UMR-CNRS 7238, Sorbonne Université, F-75005 Paris, France.ORCID 0000-0003-0772-8881
Anny Slama-SchwokCancer Biology and Therapeutics Team, INSERM, UMR_S 938, Centre de Recherche Saint-Antoine, Sorbonne Universitè, F-75012 Paris, France.ORCID 0000-0002-2703-9728
Inserm · FRUniversité Claude Bernard Lyon 1 · FRCzech Academy of Sciences, Institute of Organic Chemistry and Biochemistry · CZCentre National de la Recherche Scientifique · FRAssistance Publique – Hôpitaux de Paris · FR

Funding

AP-HP APHP200387INSERM Reacting and Merieux Foundation FR 20/02351Sorbonne University and Sorbonne Foundation CoVNucleovir
6 · The paper itself

Abstract

There is an urgent need for specific antiviral treatments directed against SARS-CoV-2 to prevent the most severe forms of COVID-19. By drug repurposing, affordable therapeutics could be supplied worldwide in the present pandemic context. Targeting the nucleoprotein N of the SARS-CoV-2 coronavirus could be a strategy to impede viral replication and possibly other essential functions associated with viral N. The antiviral properties of naproxen, a non-steroidal anti-inflammatory drug (NSAID) that was previously demonstrated to be active against Influenza A virus, were evaluated against SARS-CoV-2. Intrinsic fluorescence spectroscopy, fluorescence anisotropy, and dynamic light scattering assays demonstrated naproxen binding to the nucleoprotein of SARS-Cov-2 as predicted by molecular modeling. Naproxen impeded recombinant N oligomerization and inhibited viral replication in infected cells. In VeroE6 cells and reconstituted human primary respiratory epithelium models of SARS-CoV-2 infection, naproxen specifically inhibited viral replication and protected the bronchial epithelia against SARS-CoV-2-induced damage. No inhibition of viral replication was observed with paracetamol or the COX-2 inhibitor celecoxib. Thus, among the NSAID tested, only naproxen combined antiviral and anti-inflammatory properties. Naproxen addition to the standard of care could be beneficial in a clinical setting, as tested in an ongoing clinical study.

Indexed as

COVID-19 Drug TreatmentAnimalsAnti-Inflammatory Agents, Non-SteroidalAntiviral AgentsCell LineChlorocebus aethiopsDrug RepositioningHumansMolecular Docking SimulationNaproxenNucleoproteinsSARS-CoV-2Vero CellsViral ProteinsVirus ReplicationAnti-Inflammatory Agents, Non-SteroidalAntiviral AgentsNaproxenNucleoproteinsViral Proteinsantiviraldrug repurposinginflammationinfluenzanucleoproteinoligomerizationSARS-CoV-2structure-based drug design

Identifiers

PMID33946802
PMCPMC8124269
OpenAlexW3157146184

What OpenQuestion 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 OpenQuestion graph.