Evidence map›Paper›PMID 32560258›Full record

ReviewInternational journal of molecular sciences2020

Multiple Roles of Transforming Growth Factor Beta in Amyotrophic Lateral Sclerosis.

Mariarita Galbiati, Valeria Crippa, Paola Rusmini, Riccardo Cristofani, Elio Messi, Margherita Piccolella, Barbara Tedesco, Veronica Ferrari, Elena Casarotto, Marta Chierichetti and 1 more

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 26 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 3 pooled it
2.3field-weighted citation impact, top 9% 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

26 citing papers in PubMed, 3 syntheses or guidelines pooled it, 46 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Capacitive biophysical stimulation improves the healing of vertebral fragility fractures: a prospective multicentre randomized controlled trial.Journal of orthopaedics and traumatology : official journal of the Italian Society of Orthopaedics and Traumatology · 2024
    Trial
  5. Article
  6. Review
  7. Article
  8. IL-1ra and CCL5, but not IL-10, are promising targets for treating SMA astrocyte-driven pathology.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Knockdown ofFrontiers in cellular neuroscience · 2024
    Article
  15. Article
  16. Review
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  18. Review
  19. Profiling Secreted miRNA Biomarkers of Chemical-Induced Neurodegeneration in Human iPSC-Derived Neurons.Toxicological sciences : an official journal of the Society of Toxicology · 2022
    Article
  20. Immune Dysregulation in Autism Spectrum Disorder: What Do We Know about It?International journal of molecular sciences · 2022
    Review
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

11 authors at 1 institution in 1 country.

Mariarita GalbiatiDipartimento di Scienze Farmacologiche e Biomolecolari, Centro di Eccellenza sulle Malattie Neurodegenerative, Università degli Studi di Milano, 20133 Milano, Italy.ORCID 0000-0003-3250-5591
Valeria CrippaDipartimento di Scienze Farmacologiche e Biomolecolari, Centro di Eccellenza sulle Malattie Neurodegenerative, Università degli Studi di Milano, 20133 Milano, Italy.
Paola RusminiDipartimento di Scienze Farmacologiche e Biomolecolari, Centro di Eccellenza sulle Malattie Neurodegenerative, Università degli Studi di Milano, 20133 Milano, Italy.ORCID 0000-0001-9989-0733
Riccardo CristofaniDipartimento di Scienze Farmacologiche e Biomolecolari, Centro di Eccellenza sulle Malattie Neurodegenerative, Università degli Studi di Milano, 20133 Milano, Italy.ORCID 0000-0003-2719-846X
Elio MessiDipartimento di Scienze Farmacologiche e Biomolecolari, Centro di Eccellenza sulle Malattie Neurodegenerative, Università degli Studi di Milano, 20133 Milano, Italy.
Margherita PiccolellaDipartimento di Scienze Farmacologiche e Biomolecolari, Centro di Eccellenza sulle Malattie Neurodegenerative, Università degli Studi di Milano, 20133 Milano, Italy.
Barbara TedescoDipartimento di Scienze Farmacologiche e Biomolecolari, Centro di Eccellenza sulle Malattie Neurodegenerative, Università degli Studi di Milano, 20133 Milano, Italy.
Veronica FerrariDipartimento di Scienze Farmacologiche e Biomolecolari, Centro di Eccellenza sulle Malattie Neurodegenerative, Università degli Studi di Milano, 20133 Milano, Italy.
Elena CasarottoDipartimento di Scienze Farmacologiche e Biomolecolari, Centro di Eccellenza sulle Malattie Neurodegenerative, Università degli Studi di Milano, 20133 Milano, Italy.
Marta ChierichettiDipartimento di Scienze Farmacologiche e Biomolecolari, Centro di Eccellenza sulle Malattie Neurodegenerative, Università degli Studi di Milano, 20133 Milano, Italy.
Angelo PolettiDipartimento di Scienze Farmacologiche e Biomolecolari, Centro di Eccellenza sulle Malattie Neurodegenerative, Università degli Studi di Milano, 20133 Milano, Italy.ORCID 0000-0002-8883-0468
University of Milan · IT

Funding

Agenzia Italiana del Farmaco, Ministero della Salute Co_ALSAssociation Française contre les Myopathies 16406EU Joint Programme - Neurodegenerative Disease Research 01ED1601A, CureALSFondazione Cariplo 2014-0686Fondazione Cariplo 2017-0747Fondazione Italiana di Ricerca per la Sclerosi Laterale Amiotrofica ALS_GranulopathyFondazione Italiana di Ricerca per la Sclerosi Laterale Amiotrofica ALS_HSPB8Fondazione Italiana di Ricerca per la Sclerosi Laterale Amiotrofica Target_RANFondazione Regionale per la Ricerca Biomedica TRANS_ALSFondazione Telethon GGP14039Fondazione Telethon GGP19128Fondo per il Finanziamento delle Attività Base di Ricerca 2018Kennedy's Disease Association 2018 grantMinistero dell'Istruzione, dell'Università e della Ricerca PRIN 2015LFPNMNMinistero dell'Istruzione, dell'Università e della Ricerca PRIN 2017F2AC5Ministero dell'Istruzione, dell'Università e della Ricerca Progetto Dipartimenti di EccellenzaUniversità degli Studi di Milano Bando SEED 2019: #TDP-43-iPSCUniversità degli Studi di Milano Piano di sviluppo UNIMI - linea B
6 · The paper itself

Abstract

Transforming growth factor beta (TGFB) is a pleiotropic cytokine known to be dysregulated in many neurodegenerative disorders and particularly in amyotrophic lateral sclerosis (ALS). This motor neuronal disease is non-cell autonomous, as it affects not only motor neurons but also the surrounding glial cells, and the target skeletal muscle fibers. Here, we analyze the multiple roles of TGFB in these cell types, and how TGFB signaling is altered in ALS tissues. Data reported support a crucial involvement of TGFB in the etiology and progression of ALS, leading us to hypothesize that an imbalance of TGFB signaling, diminished at the pre-symptomatic stage and then increased with time, could be linked to ALS progression. A reduced stimulation of the TGFB pathway at the beginning of disease blocks its neuroprotective effects and promotes glutamate excitotoxicity. At later disease stages, the persistent activation of the TGFB pathway promotes an excessive microglial activation and strengthens muscular dysfunction. The therapeutic potential of TGFB is discussed, in order to foster new approaches to treat ALS.

Indexed as

Amyotrophic Lateral SclerosisGene Expression RegulationGlutamic AcidHumansMotor NeuronsMuscle Fibers, SkeletalNeurogliaSignal TransductionTransforming Growth Factor betaGlutamic AcidTransforming Growth Factor betaALSglial cellsmotor neuronskeletal muscleTGFB

Identifiers

PMID32560258
PMCPMC7352289
OpenAlexW3034178500

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.