Evidence map›Paper›PMID 36054466›Full record

ReviewThe Journal of physiology2022

Involvement of the extracellular matrix and integrin signalling proteins in skeletal muscle glucose uptake.

Fulvia Draicchio, Volker Behrends, Neale A Tillin, Nicholas M Hurren, Lykke Sylow, Richard Mackenzie

Open access · hybridAbstract readReview
In one paragraph

Review in The Journal of physiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

14 citing papers in PubMed, 21 citations in OpenAlex.

  1. Trial
  2. Relaxin-2: Shaping the Proteomic Landscape of Skeletal Muscle Physiology, Glucose Trafficking, and Mitochondrial Function in Rat.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  3. Article
  4. Article
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  6. Focal Adhesion Kinase Orchestrates GLUT4 Translocation and Glucose Uptake via Cytoskeletal Turnover in Primary Adipocytes.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. 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

6 authors at 2 institutions in 2 countries.

Fulvia DraicchioSchool of Life and Health Sciences, Whitelands College, University of Roehampton, London, UK.ORCID 0000-0002-5686-3054
Volker BehrendsSchool of Life and Health Sciences, Whitelands College, University of Roehampton, London, UK.
Neale A TillinSchool of Life and Health Sciences, Whitelands College, University of Roehampton, London, UK.ORCID 0000-0003-0000-8670
Nicholas M HurrenSchool of Life and Health Sciences, Whitelands College, University of Roehampton, London, UK.
Lykke SylowMolecular Metabolism in Cancer & Ageing Research Group, Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.ORCID 0000-0003-0905-5932
Richard MackenzieSchool of Life and Health Sciences, Whitelands College, University of Roehampton, London, UK.ORCID 0000-0001-6799-6218
University of Roehampton · GBUniversity of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Whole-body euglycaemia is partly maintained by two cellular processes that encourage glucose uptake in skeletal muscle, the insulin- and contraction-stimulated pathways, with research suggesting convergence between these two processes. The normal structural integrity of the skeletal muscle requires an intact actin cytoskeleton as well as integrin-associated proteins, and thus those structures are likely fundamental for effective glucose uptake in skeletal muscle. In contrast, excessive extracellular matrix (ECM) remodelling and integrin expression in skeletal muscle may contribute to insulin resistance owing to an increased physical barrier causing reduced nutrient and hormonal flux. This review explores the role of the ECM and the actin cytoskeleton in insulin- and contraction-mediated glucose uptake in skeletal muscle. This is a clinically important area of research given that defects in the structural integrity of the ECM and integrin-associated proteins may contribute to loss of muscle function and decreased glucose uptake in type 2 diabetes.

Indexed as

Diabetes Mellitus, Type 2GlucoseExtracellular MatrixHumansInsulinIntegrinsMuscle, SkeletalGlucoseInsulinIntegrinsactin cytoskeletonECMILKinsulininsulin resistanceintegrinmuscle contractionRac1

Identifiers

PMID36054466
PMCPMC9826115
OpenAlexW4294316574

What Socratic 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 Socratic graph.