Evidence map›Paper›PMID 33740184›Full record

ReviewMolecular and cellular biochemistry2021

Possible role of purinergic signaling in COVID-19.

Maria Luiza Mukai Franciosi, Millena Daher Medeiros Lima, Maria Rosa Chitolina Schetinger, Andréia Machado Cardoso

Open access · bronzeAbstract readReview
In one paragraph

Review in Molecular and cellular biochemistry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
5.5field-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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 37 citations in OpenAlex.

  1. Pooled it
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  7. Article
  8. Article
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  10. Article
  11. CD73: Friend or Foe in Lung Injury.International journal of molecular sciences · 2023
    Review
  12. The ATP-dependent Pathways and Human Diseases.Current medicinal chemistry · 2023
    Article
  13. Review
  14. Review
  15. Review
  16. 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

4 authors at 2 institutions in 1 country.

Maria Luiza Mukai FranciosiMedicine Course, Federal University of Fronteira Sul, Campus Chapecó, Chapecó, SC, Brazil.ORCID http://orcid.org/0000-0002-4675-062X
Millena Daher Medeiros LimaMedicine Course, Federal University of Fronteira Sul, Campus Chapecó, Chapecó, SC, Brazil.ORCID http://orcid.org/0000-0003-4940-8894
Maria Rosa Chitolina SchetingerPost-Graduation Program in Biological Sciences: Toxicological Biochemistry, CCNE, Federal University of Santa Maria, Santa Maria, RS, Brazil.ORCID http://orcid.org/0000-0002-5240-8935
Andréia Machado CardosoGraduate Program in Biomedical Sciences, Medicine Course, Member of the Brazilian Purine Club, Federal University of Fronteira Sul, Fronteira Sul, Campus Chapecó, Rodovia SC 484 - Km 02, Chapecó, SC, 89815-899, Brazil. andreia.cardoso@uffs.edu.br.ORCID http://orcid.org/0000-0003-4243-8855
Universidade Federal da Fronteira Sul · BRUniversidade Federal de Santa Maria · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The coronavirus disease (COVID-19), caused by SARS-CoV-2 infection, accounts for more than 2.4 million deaths worldwide, making it the main public health problem in 2020. Purinergic signaling is involved in the pathophysiology of several viral infections which makes the purinergic system a potential target of investigation in COVID-19. During viral infections, the ATP release initiates a cascade that activates purinergic receptors. This receptor activation enhances the secretion of pro-inflammatory cytokines and performs the chemotaxis of macrophages and neutrophils, generating an association between the immune and the purinergic systems. This review was designed to cover the possible functions of purinergic signaling in COVID-19, focusing on the possible role of purinergic receptors such as P2X7 which contributes to cytokine storm and inflammasome NLRP3 activation and P2Y1 that activates the blood coagulation pathway. The possible role of ectonucleotidases, such as CD39 and CD73, which have the function of dephosphorylating ATP in an immunosuppressive component, adenosine, are also covered in detail. Moreover, therapeutic combination or association possibilities targeting purinergic system components are also suggested as a possible useful tool to be tested in future researches, aiming to unveil a novel option to treat COVID-19 patients.

Indexed as

Signal TransductionAnimalsCOVID-19HumansModels, BiologicalMolecular Targeted TherapyReceptors, PurinergicSARS-CoV-2Receptors, PurinergicAdenosineATPCOVID-19EctonucleotidasesPurinergic Signaling

Identifiers

PMID33740184
PMCPMC7973800
OpenAlexW3139477938

What OpenQuestion holds

Textmetadata
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.