Evidence map›Paper›PMID 32630118›Full record

ReviewInternational journal of molecular sciences2020

Emerging Strategies Targeting Catabolic Muscle Stress Relief.

Mattia Scalabrin, Volker Adams, Siegfried Labeit, T Scott Bowen

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 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

11 citing papers in PubMed, 17 citations in OpenAlex.

  1. Puerarin-RichPreventive nutrition and food science · 2026
    Article
  2. Review
  3. Frontiers in pharmacology · 2024
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Molecular Mechanisms Underlying Muscle Wasting in Huntington's Disease.International journal of molecular sciences · 2020
    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

4 authors at 3 institutions in 2 countries.

Mattia ScalabrinSchool of Biomedical Sciences, University of Leeds, LS2 9JT Leeds, UK.
Volker AdamsDepartment of Experimental and Molecular Cardiology, TU Dresden, Heart Center Dresden, 01307 Dresden, Germany.
Siegfried LabeitMedical Faculty Mannheim, University of Heidelberg, 68167 Mannheim, Germany.
T Scott BowenSchool of Biomedical Sciences, University of Leeds, LS2 9JT Leeds, UK.
University of Leeds · GBHeidelberg University · DETechnische Universität Dresden · DE

Funding

Heart Research UK TRP 16/19Medical Research Council MR/S025472/1
6 · The paper itself

Abstract

Skeletal muscle wasting represents a common trait in many conditions, including aging, cancer, heart failure, immobilization, and critical illness. Loss of muscle mass leads to impaired functional mobility and severely impedes the quality of life. At present, exercise training remains the only proven treatment for muscle atrophy, yet many patients are too ill, frail, bedridden, or neurologically impaired to perform physical exertion. The development of novel therapeutic strategies that can be applied to an in vivo context and attenuate secondary myopathies represents an unmet medical need. This review discusses recent progress in understanding the molecular pathways involved in regulating skeletal muscle wasting with a focus on pro-catabolic factors, in particular, the ubiquitin-proteasome system and its activating muscle-specific E3 ligase RING-finger protein 1 (MuRF1). Mechanistic progress has provided the opportunity to design experimental therapeutic concepts that may affect the ubiquitin-proteasome system and prevent subsequent muscle wasting, with novel advances made in regards to nutritional supplements, nuclear factor kappa-light-chain-enhancer of activated B cells (NFB) inhibitors, myostatin antibodies, β

Indexed as

Molecular Targeted TherapyAnimalsHumansMuscle ProteinsMuscular AtrophyProteasome Endopeptidase ComplexTripartite Motif ProteinsUbiquitinUbiquitin-Protein LigasesMuscle ProteinsProteasome Endopeptidase ComplexTRIM63 protein, humanTripartite Motif ProteinsUbiquitinUbiquitin-Protein LigasesatrophydiaphragmdisusemitochondriaMuRF1MuRF2skeletal muscleubiquitinwasting

Identifiers

PMID32630118
PMCPMC7369951
OpenAlexW3040126216

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.