Evidence map›Paper›PMID 28545587›Full record

ArticleGenome medicine2017

Type 2 diabetes and obesity induce similar transcriptional reprogramming in human myocytes.

Leif Väremo, Tora Ida Henriksen, Camilla Scheele, Christa Broholm, Maria Pedersen, Mathias Uhlén, Bente Klarlund Pedersen, Jens Nielsen

Open access · goldAbstract read
In one paragraph

Article in Genome medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.0field-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

25 citing papers in PubMed, 45 citations in OpenAlex.

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  11. Biophysics reviews · 2022
    Review
  12. Article
  13. Article
  14. The Potential Role of Gut Microbiota in the Pathogenesis of Type 2 Diabetes MellitusEndocrine, metabolic & immune disorders drug targets · 2022
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Mitochondrial Function in Muscle Stem Cell Fates.Frontiers in cell and developmental biology · 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

8 authors at 3 institutions in 2 countries.

Leif VäremoDepartment of Biology and Biological Engineering, Chalmers University of Technology, 41296, Gothenburg, Sweden.
Tora Ida HenriksenCentre of Inflammation and Metabolism and Centre for Physical Activity Research, Rigshospitalet, University of Copenhagen, 2100, Copenhagen Ø, Denmark.
Camilla ScheeleCentre of Inflammation and Metabolism and Centre for Physical Activity Research, Rigshospitalet, University of Copenhagen, 2100, Copenhagen Ø, Denmark.
Christa BroholmCentre of Inflammation and Metabolism and Centre for Physical Activity Research, Rigshospitalet, University of Copenhagen, 2100, Copenhagen Ø, Denmark.
Maria PedersenCentre of Inflammation and Metabolism and Centre for Physical Activity Research, Rigshospitalet, University of Copenhagen, 2100, Copenhagen Ø, Denmark.
Mathias UhlénDepartment of Proteomics, School of Biotechnology, AlbaNova University Center, Royal Institute of Technology (KTH), 10691, Stockholm, Sweden.
Bente Klarlund PedersenCentre of Inflammation and Metabolism and Centre for Physical Activity Research, Rigshospitalet, University of Copenhagen, 2100, Copenhagen Ø, Denmark.
Jens NielsenDepartment of Biology and Biological Engineering, Chalmers University of Technology, 41296, Gothenburg, Sweden. nielsenj@chalmers.se.ORCID 0000-0002-9955-6003
University of Copenhagen · DKScience for Life Laboratory · SEChalmers University of Technology · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSkeletal muscle is one of the primary tissues involved in the development of type 2 diabetes (T2D). The close association between obesity and T2D makes it difficult to isolate specific effects attributed to the disease alone. Therefore, here we set out to identify and characterize intrinsic properties of myocytes, associated independently with T2D or obesity.

methodsWe generated and analyzed RNA-seq data from primary differentiated myotubes from 24 human subjects, using a factorial design (healthy/T2D and non-obese/obese), to determine the influence of each specific factor on genome-wide transcription. This setup enabled us to identify intrinsic properties, originating from muscle precursor cells and retained in the corresponding myocytes. Bioinformatic and statistical methods, including differential expression analysis, gene-set analysis, and metabolic network analysis, were used to characterize the different myocytes.

resultsWe found that the transcriptional program associated with obesity alone was strikingly similar to that induced specifically by T2D. We identified a candidate epigenetic mechanism, H3K27me3 histone methylation, mediating these transcriptional signatures. T2D and obesity were independently associated with dysregulated myogenesis, down-regulated muscle function, and up-regulation of inflammation and extracellular matrix components. Metabolic network analysis identified that in T2D but not obesity a specific metabolite subnetwork involved in sphingolipid metabolism was transcriptionally regulated.

conclusionsOur findings identify inherent characteristics in myocytes, as a memory of the in vivo phenotype, without the influence from a diabetic or obese extracellular environment, highlighting their importance in the development of T2D.

Indexed as

Epigenesis, GeneticAdultComputational BiologyDiabetes Mellitus, Type 2FemaleHistonesHumansInflammationMaleMethylationMiddle AgedMuscle DevelopmentMuscle Fibers, SkeletalObesitySequence Analysis, RNASphingolipidsHistonesSphingolipidsGene expressionGene-set analysisMetabolic networkObesityRNA-seqSkeletal myocytesType 2 diabetes

Identifiers

PMID28545587
PMCPMC5444103
OpenAlexW2618293190

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Registered trials

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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.