Evidence map›Paper›PMID 30867438›Full record

ArticleScientific reports2019

The immunosuppressant drug azathioprine restrains adipogenesis of muscle Fibro/Adipogenic Progenitors from dystrophic mice by affecting AKT signaling.

Alessio Reggio, Filomena Spada, Marco Rosina, Giorgia Massacci, Alessandro Zuccotti, Claudia Fuoco, Cesare Gargioli, Luisa Castagnoli, Gianni Cesareni

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

22 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Muscle Health & Fatty Infiltration with Advanced Rotator Cuff Pathology.Current reviews in musculoskeletal medicine · 2025
    Review
  7. PdgfrαGenes & diseases · 2025
    Review
  8. Vascular adhesion molecule 1JVS-vascular science · 2025
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Adipokine Signaling Pathways in Osteoarthritis.Frontiers in bioengineering and biotechnology · 2022
    Review
  15. Review
  16. Review
  17. Review
  18. Article
  19. Article
  20. 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

9 authors at 1 institution in 1 country.

Alessio ReggioDepartment of Biology, University of Rome "Tor Vergata", 00133, Rome, Italy.ORCID 0000-0001-5333-7502
Filomena SpadaDepartment of Biology, University of Rome "Tor Vergata", 00133, Rome, Italy.
Marco RosinaDepartment of Biology, University of Rome "Tor Vergata", 00133, Rome, Italy.ORCID 0000-0003-0952-1710
Giorgia MassacciDepartment of Biology, University of Rome "Tor Vergata", 00133, Rome, Italy.
Alessandro ZuccottiDepartment of Biology, University of Rome "Tor Vergata", 00133, Rome, Italy.
Claudia FuocoDepartment of Biology, University of Rome "Tor Vergata", 00133, Rome, Italy.
Cesare GargioliDepartment of Biology, University of Rome "Tor Vergata", 00133, Rome, Italy.
Luisa CastagnoliDepartment of Biology, University of Rome "Tor Vergata", 00133, Rome, Italy. castagnoli@uniroma2.it.
Gianni CesareniDepartment of Biology, University of Rome "Tor Vergata", 00133, Rome, Italy. cesareni@uniroma2.it.ORCID 0000-0002-9528-6018
University of Rome Tor Vergata · IT

Funding

European Research Council 322749
6 · The paper itself

Abstract

Fibro/Adipogenic Progenitors (FAPs) define a stem cell population playing a pro-regenerative role after muscle damage. When removed from their natural niche, FAPs readily differentiate into adipocytes or fibroblasts. This digressive differentiation potential, which is kept under tight control in the healthy muscle niche, contributes to fat and scar infiltrations in degenerative myopathies, such as in Duchenne Muscular Dystrophy (DMD). Controlling FAP differentiation by means of small molecules may contribute to delay the adverse consequences of the progressive pathological degeneration while offering, at the same time, a wider temporal window for gene therapy and cell-based strategies. In a high content phenotypic screening, we identified the immunosuppressant, azathioprine (AZA) as a negative modulator of FAP adipogenesis. We show here that AZA negatively affects the adipogenic propensity of FAPs purified from wild type and mdx mice by impairing the expression of the master adipogenic regulator, peroxisome proliferator-activated receptor γ (PPARγ). We show that this inhibition correlates with a decline in the activation of the AKT-mTOR axis, the main pathway that transduces the pro-adipogenic stimulus triggered by insulin. In addition, AZA exerts a cytostatic effect that has a negative impact on the mitotic clonal process that is required for the terminal differentiation of the preadipocyte-committed cells.

Indexed as

AdipogenesisAnimalsAzathioprineCell DifferentiationCells, CulturedDisease Models, AnimalFibroblastsImmunosuppressive AgentsMiceMice, Inbred mdxModels, BiologicalMuscular Dystrophy, DuchenneMyoblasts, SkeletalPPAR gammaProto-Oncogene Proteins c-aktSignal TransductionAzathioprineImmunosuppressive AgentsPPAR gammaProto-Oncogene Proteins c-aktTOR Serine-Threonine Kinases

Identifiers

PMID30867438
PMCPMC6416262
OpenAlexW2921269123

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.