Evidence map›Paper›PMID 32900951›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

Dynamic changes in DICER levels in adipose tissue control metabolic adaptations to exercise.

Bruna B Brandão, Søren Madsen, Atefeh Rabiee, Matteo Oliverio, Gabriel P Ruiz, Danilo L Ferrucci, Jéssica L Branquinho, Daniela Razolli, Silas Pinto, Thomas S Nielsen and 16 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.6field-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

23 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. DICER-driven regulation of lipid metabolism and macrophage-adipocyte crosstalk in partial lipodystrophy.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2026
    Article
  3. Article
  4. Adipose Dicer-1 modulates systemic insulin signaling and longevity via a miR-8-Aop-Dilp6 axis.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. MicroRNAs in diabetic macroangiopathy.Cardiovascular diabetology · 2024
    Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. FOXO-mediated repression of Dicer1 regulates metabolism, stress resistance, and longevity inProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  17. MicroRNA biogenesis pathway alterations in aging.Extracellular vesicles and circulating nucleic acids · 2023
    Review
  18. Article
  19. Review
  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

26 authors at 9 institutions in 6 countries.

Bruna B BrandãoProgram in Molecular Biology, Federal University of São Paulo, 04044-020 São Paulo, Brazil.ORCID 0000-0001-8762-6310
Søren MadsenIntegrative Metabolism and Environmental Influences, Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health Sciences, University of Copenhagen, DK-2200 Copenhagen, Denmark.ORCID 0000-0002-1585-7862
Atefeh RabieeIntegrative Metabolism and Environmental Influences, Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health Sciences, University of Copenhagen, DK-2200 Copenhagen, Denmark.
Matteo OliverioLaboratory of Non-Coding Principles of Energy Homeostasis, Max Planck Institute for Metabolism Research, 50931 Cologne, Germany.ORCID 0000-0002-7969-2796
Gabriel P RuizProgram in Genetics and Molecular Biology, Institute of Biology, University of Campinas, 13083-862 São Paulo, Brazil.
Danilo L FerrucciDepartment of Biochemistry and Tissue Biology, Institute of Biology, University of Campinas, 13083-862 São Paulo, Brazil.
Jéssica L BranquinhoProgram in Molecular Biology, Federal University of São Paulo, 04044-020 São Paulo, Brazil.
Daniela RazolliObesity and Comorbidities Research Center, University of Campinas, 13083-862 Campinas, Brazil.ORCID 0000-0002-2217-0946
Silas PintoProgram in Genetics and Molecular Biology, Institute of Biology, University of Campinas, 13083-862 São Paulo, Brazil.
Thomas S NielsenIntegrative Metabolism and Environmental Influences, Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health Sciences, University of Copenhagen, DK-2200 Copenhagen, Denmark.ORCID 0000-0002-9457-8000
William T FestucciaDepartment of Physiology, Institute of Biomedical Sciences, University of São Paulo, 05508-000 São Paulo, Brazil.
Adriano S MartinsProgram in Molecular Biology, Federal University of São Paulo, 04044-020 São Paulo, Brazil.ORCID 0000-0001-5747-5945
Beatriz A GuerraProgram in Molecular Biology, Federal University of São Paulo, 04044-020 São Paulo, Brazil.
Thiago L KnittelProgram in Genetics and Molecular Biology, Institute of Biology, University of Campinas, 13083-862 São Paulo, Brazil.
Ditte SøgaardDepartment of Biomedical Sciences, Center of Healthy Aging, University of Copenhagen, DK-2200 Copenhagen, Denmark.
Steen LarsenDepartment of Biomedical Sciences, Center of Healthy Aging, University of Copenhagen, DK-2200 Copenhagen, Denmark.
Jørn W HelgeDepartment of Biomedical Sciences, Center of Healthy Aging, University of Copenhagen, DK-2200 Copenhagen, Denmark.ORCID 0000-0001-9724-5423
Josef BrandauerDepartment of Health Sciences, Gettysburg College, Gettysburg, PA 17325.
Lício A VellosoObesity and Comorbidities Research Center, University of Campinas, 13083-862 Campinas, Brazil.ORCID 0000-0002-4806-7218
Brice EmanuelliIntegrative Metabolism and Environmental Influences, Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health Sciences, University of Copenhagen, DK-2200 Copenhagen, Denmark.ORCID 0000-0001-5795-5666
Jan-Wilhelm KornfeldDepartment for Biochemistry and Molecular Biology, University of Southern Denmark, DK-5230 Odense, Denmark.
C Ronald KahnSection on Integrative Physiology and Metabolism, Joslin Diabetes Center, Harvard Medical School, Boston, MA 02215; c.ronald.kahn@joslin.harvard.edu jttreebak@sund.ku.dk morima@unicamp.br.ORCID 0000-0002-7583-9228
Sara G VienbergIntegrative Metabolism and Environmental Influences, Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health Sciences, University of Copenhagen, DK-2200 Copenhagen, Denmark.
Juleen R ZierathIntegrative Metabolism and Environmental Influences, Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health Sciences, University of Copenhagen, DK-2200 Copenhagen, Denmark.
Jonas T TreebakIntegrative Metabolism and Environmental Influences, Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health Sciences, University of Copenhagen, DK-2200 Copenhagen, Denmark; c.ronald.kahn@joslin.harvard.edu jttreebak@sund.ku.dk morima@unicamp.br.ORCID 0000-0003-1488-7012
Marcelo A MoriProgram in Molecular Biology, Federal University of São Paulo, 04044-020 São Paulo, Brazil; c.ronald.kahn@joslin.harvard.edu jttreebak@sund.ku.dk morima@unicamp.br.ORCID 0000-0001-7112-5263
University of Copenhagen · DKUniversidade Estadual de Campinas (UNICAMP) · BRJoslin Diabetes Center · USGettysburg College · USMaimonides Medical Center · USMax Planck Institute for Metabolism Research · DEUniversidade de São Paulo · BRUniversidade Federal de São Paulo · BRUniversity of Southern Denmark · DK

Funding

Developmental genes, miRNAs and adipose tissueR01DK082659 · NIDDK · JOSLIN DIABETES CENTER · PI C RONALD KAHN · 2009 to 2026
$10.7M
NIDDK NIH HHS R01 DK082659
6 · The paper itself

Abstract

DICER is a key enzyme in microRNA (miRNA) biogenesis. Here we show that aerobic exercise training up-regulates DICER in adipose tissue of mice and humans. This can be mimicked by infusion of serum from exercised mice into sedentary mice and depends on AMPK-mediated signaling in both muscle and adipocytes. Adipocyte DICER is required for whole-body metabolic adaptations to aerobic exercise training, in part, by allowing controlled substrate utilization in adipose tissue, which, in turn, supports skeletal muscle function. Exercise training increases overall miRNA expression in adipose tissue, and up-regulation of miR-203-3p limits glycolysis in adipose under conditions of metabolic stress. We propose that exercise training-induced DICER-miR-203-3p up-regulation in adipocytes is a key adaptive response that coordinates signals from working muscle to promote whole-body metabolic adaptations.

Indexed as

Adaptation, PhysiologicalAdipocytesAdipose TissueAMP-Activated Protein KinasesAnimalsCells, CulturedDEAD-box RNA HelicasesExerciseFemaleGlycolysisHumansMaleMiceMice, KnockoutMicroRNAsPhysical Conditioning, AnimalAMP-Activated Protein KinasesDEAD-box RNA HelicasesDICER1 protein, humanDicer1 protein, mouseMicroRNAsMIRN203 microRNA, humanMIRN203 microRNA, mouseRibonuclease IIIadipose tissuecross-talkexercisemetabolic flexibilitymicroRNA

Identifiers

PMID32900951
PMCPMC7519274
OpenAlexW3084265334

What OpenQuestion holds

Textmetadata
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.