Evidence map›Paper›PMID 29895328›Full record

ArticleBMC biology2018

Glucocorticoid-dependent REDD1 expression reduces muscle metabolism to enable adaptation under energetic stress.

Florian A Britto, Fabienne Cortade, Yassine Belloum, Marine Blaquière, Yann S Gallot, Aurélie Docquier, Allan F Pagano, Elodie Jublanc, Nadia Bendridi, Christelle Koechlin-Ramonatxo and 9 more

Open access · goldAbstract read
In one paragraph

Article in BMC biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

30 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Article
  3. Nomilin Rewires mTOR-Driven Immunometabolism via DDIT4 to Restrain Psoriasis.International journal of biological sciences · 2026
    Article
  4. Review
  5. Article
  6. Article
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  8. Article
  9. Article
  10. Review
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  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Nutritional Sensor REDD1 in Cancer and Inflammation: Friend or Foe?International journal of molecular sciences · 2022
    Review
  18. Article
  19. Article
  20. 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

19 authors at 6 institutions in 2 countries.

Florian A BrittoDMEM, Univ. Montpellier, INRA, Montpellier, France.
Fabienne CortadeDMEM, Univ. Montpellier, INRA, Montpellier, France.
Yassine BelloumDMEM, Univ. Montpellier, INRA, Montpellier, France.
Marine BlaquièrePHYMEDEXP, Univ. Montpellier, INSERM, CNRS, CHRU of Montpellier, Montpellier, France.
Yann S GallotLIBM, Univ. Lyon, Saint Etienne, France.
Aurélie DocquierDMEM, Univ. Montpellier, INRA, Montpellier, France.
Allan F PaganoDMEM, Univ. Montpellier, INRA, Montpellier, France.
Elodie JublancDMEM, Univ. Montpellier, INRA, Montpellier, France.
Nadia BendridiINSERM UMR-1060, CarMeN Laboratory, Lyon 1 University, INRA U1397, Oullins, France.
Christelle Koechlin-RamonatxoDMEM, Univ. Montpellier, INRA, Montpellier, France.
Béatrice ChabiDMEM, Univ. Montpellier, INRA, Montpellier, France.
Marc FrancauxInstitute of Neuroscience, Université catholique de Louvain, Louvain-la-Neuve, Belgium.
François CasasDMEM, Univ. Montpellier, INRA, Montpellier, France.
Damien FreyssenetLIBM, Univ. Lyon, Saint Etienne, France.
Jennifer RieussetINSERM UMR-1060, CarMeN Laboratory, Lyon 1 University, INRA U1397, Oullins, France.
Sophie Giorgetti-PeraldiUniversité Cote d'Azur, INSERM, UMR1065, C3M, Nice, France.
Gilles CarnacPHYMEDEXP, Univ. Montpellier, INSERM, CNRS, CHRU of Montpellier, Montpellier, France.
Vincent OllendorffDMEM, Univ. Montpellier, INRA, Montpellier, France. vincent.ollendorff@inra.fr.
François B FavierDMEM, Univ. Montpellier, INRA, Montpellier, France. francois.favier@umontpellier.fr.
Université de Montpellier · FRUniversité Claude Bernard Lyon 1 · FRCentre National de la Recherche Scientifique · FRDynamique Musculaire et MétabolismeUCLouvain · BEUniversité Côte d'Azur · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSkeletal muscle atrophy is a common feature of numerous chronic pathologies and is correlated with patient mortality. The REDD1 protein is currently recognized as a negative regulator of muscle mass through inhibition of the Akt/mTORC1 signaling pathway. REDD1 expression is notably induced following glucocorticoid secretion, which is a component of energy stress responses.

resultsUnexpectedly, we show here that REDD1 instead limits muscle loss during energetic stresses such as hypoxia and fasting by reducing glycogen depletion and AMPK activation. Indeed, we demonstrate that REDD1 is required to decrease O

conclusionsTherefore, REDD1 is a crucial negative regulator of energy expenditure that is necessary for muscle adaptation during energetic stresses. This present study could shed new light on the role of REDD1 in several pathologies associated with energetic metabolism alteration, such as cancer, diabetes, and Parkinson's disease.

Indexed as

Adaptation, PhysiologicalAnimalsCell HypoxiaEnergy MetabolismHumansMechanistic Target of Rapamycin Complex 1MiceMitochondria, MuscleMuscle, SkeletalMuscular AtrophySignal TransductionStress, PhysiologicalTranscription FactorsDdit4 protein, mouseMechanistic Target of Rapamycin Complex 1Transcription FactorsEnergy expenditureExerciseFastingHypoxiaMAMsMetabolismMitochondriamTORSkeletal muscle

Identifiers

PMID29895328
PMCPMC5998563
OpenAlexW2808276527

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.