Evidence map›Paper›PMID 32825102›Full record

ReviewInternational journal of molecular sciences2020

eATP/P2X7R Axis: An Orchestrated Pathway Triggering Inflammasome Activation in Muscle Diseases.

Chiara Panicucci, Lizzia Raffaghello, Santina Bruzzone, Serena Baratto, Elisa Principi, Carlo Minetti, Elisabetta Gazzerro, Claudio Bruno

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

18 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Exercise as a modulator of purinergic signaling and inflammation in cancer-associated sarcopenia: a narrative review.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Review
  3. Article
  4. Review
  5. Genetic Deletion of the Purinergic ReceptorACS pharmacology & translational science · 2025
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Special Issue ofInternational journal of molecular sciences · 2020
    Article
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

8 authors at 3 institutions in 2 countries.

Chiara PanicucciCenter of Translational and Experimental Myology, IRCCS Istituto Giannina Gaslini, 16147 Genova, Italy.
Lizzia RaffaghelloCenter of Translational and Experimental Myology, IRCCS Istituto Giannina Gaslini, 16147 Genova, Italy.
Santina BruzzoneDepartment of Experimental Medicine, University of Genova, 16126 Genova, Italy.
Serena BarattoCenter of Translational and Experimental Myology, IRCCS Istituto Giannina Gaslini, 16147 Genova, Italy.
Elisa PrincipiCenter of Translational and Experimental Myology, IRCCS Istituto Giannina Gaslini, 16147 Genova, Italy.
Carlo MinettiPediatric Neurology Unit, IRCCS Istituto Giannina Gaslini, and University of Genova, 16147 Genova, Italy.
Elisabetta GazzerroUnit of Muscle Research, Experimental and Clinical Research Center Charité Universitätsmedizin and Max Delbrück Research Center, 13125 Berlin, Germany.
Claudio BrunoCenter of Translational and Experimental Myology, IRCCS Istituto Giannina Gaslini, 16147 Genova, Italy.
Istituto Giannina Gaslini · ITMax Delbrück Center · DEUniversity of Genoa · IT

Funding

Fondazione Telethon GGP17192Italian Ministry of Health RF 2016-02364503
6 · The paper itself

Abstract

In muscle ATP is primarily known for its function as an energy source and as a mediator of the "excitation-transcription" process, which guarantees muscle plasticity in response to environmental stimuli. When quickly released in massive concentrations in the extracellular space as in presence of muscle membrane damage, ATP acts as a damage-associated molecular pattern molecule (DAMP). In experimental murine models of muscular dystrophies characterized by membrane instability, blockade of eATP/P2X7 receptor (R) purinergic signaling delayed the progression of the dystrophic phenotype dampening the local inflammatory response and inducing Foxp3

Indexed as

Adenosine TriphosphateAnimalsHumansInflammasomesMuscle, SkeletalMuscular DystrophiesReceptors, Purinergic P2X7Signal TransductionAdenosine TriphosphateInflammasomesReceptors, Purinergic P2X7Duchenne Muscular DystrophyeATPinflammasomemuscular dystrophiesP2X7RSarcoglycanopathies

Identifiers

PMID32825102
PMCPMC7504480
OpenAlexW3053105202

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.