Evidence map›Paper›PMID 32441764›Full record

ReviewBritish journal of pharmacology2020

Repositioning PARP inhibitors for SARS-CoV-2 infection(COVID-19); a new multi-pronged therapy for acute respiratory distress syndrome?

Nicola Curtin, Krisztián Bányai, James Thaventhiran, John Le Quesne, Zsuzsanna Helyes, Péter Bai

Open access · bronzeAbstract readReview
In one paragraph

Review in British journal of pharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
4.4field-weighted citation impact, top 4% 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

43 citing papers in PubMed, 66 citations in OpenAlex.

  1. Article
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  10. SARS-CoV-2 and the DNA damage response.The Journal of general virology · 2023
    Review
  11. Article
  12. Article
  13. Involvement of epigenetics in affecting host immunity during SARS-CoV-2 infection.Biochimica et biophysica acta. Molecular basis of disease · 2023
    Review
  14. Review
  15. Article
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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

6 authors at 6 institutions in 2 countries.

Nicola CurtinTranslational and Clinical Research Institute, Newcastle University Centre for Cancer, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK.
Krisztián BányaiInstitute for Veterinary Medical Research, Centre for Agricultural Research, Budapest, Hungary.
James ThaventhiranMRC Toxicology Unit, University of Cambridge, Leicester, UK.
John Le QuesneMRC Toxicology Unit, University of Cambridge, Leicester, UK.
Zsuzsanna HelyesDepartment of Pharmacology and Pharmacotherapy, Medical School; Centre for Neuroscience and János Szentágothai Research Centre, University of Pécs, Pécs, Hungary.
Péter BaiDepartment of Medical Chemistry, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.ORCID 0000-0002-6191-6616
HUN-REN Veterinary Medical Research Institute · HUNewcastle University · GBUniversity of Cambridge · GBUniversity of Debrecen · HUUniversity of Leicester · GBUniversity of Pecs · HU

Funding

Faculty of Medicine at the University of DebrecenHungarian Scientific Research Fund 20765-3/2018/FEKUTSTRATHungarian Scientific Research Fund EFOP-3.6.2-16-2017-00008Hungarian Scientific Research Fund GINOP-2.3.2-15-2016-0000Hungarian Scientific Research Fund GINOP-2.3.2 STAY ALIVEHungarian Scientific Research Fund K123975Hungarian Scientific Research Fund NKFIH-1150-6/2019Medical Research Council MC_UP_1203/1
6 · The paper itself

Abstract

Clinically approved PARP inhibitors (PARPi) have a mild adverse effect profile and are well tolerated as continuous daily oral therapy. We review the evidence that justifies the repurposing of PARPi to block the proliferation of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and combat the life-threatening sequelae of coronavirus disease 2019 (COVID-19) by several mechanisms. PARPi can effectively decrease IL-6, IL-1 and TNF-α levels (key interleukins in SARS-CoV-2-induced cytokine storm) and can alleviate subsequent lung fibrosis, as demonstrated in murine experiments and clinical trials. PARPi can tune macrophages towards a tolerogenic phenotype. PARPi may also counteract SARS-CoV-2-induced and inflammation-induced cell death and support cell survival. PARPi is effective in animal models of acute respiratory distress syndrome (ARDS), asthma and ventilator-induced lung injury. PARPi may potentiate the effectiveness of tocilizumab, anakinra, sarilumab, adalimumab, canakinumab or siltuximab therapy. The evidence suggests that PARPi would benefit COVID-19 patients and trials should be undertaken.

Indexed as

BetacoronavirusCoronavirus InfectionsCOVID-19HumansPandemicsPneumonia, ViralPoly(ADP-ribose) Polymerase InhibitorsSARS-CoV-2Poly(ADP-ribose) Polymerase Inhibitors

Identifiers

PMID32441764
PMCPMC7280733
OpenAlexW3026749139

What OpenQuestion holds

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LicenceCC BY-NC
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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.