Evidence map›Paper›PMID 33257663›Full record

ArticleNature communications2020

Lkb1 suppresses amino acid-driven gluconeogenesis in the liver.

Pierre-Alexandre Just, Sara Charawi, Raphaël G P Denis, Mathilde Savall, Massiré Traore, Marc Foretz, Sultan Bastu, Salimata Magassa, Nadia Senni, Pierre Sohier and 12 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 24 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 2 pooled it
1.8field-weighted citation impact, top 14% 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

24 citing papers in PubMed, 2 syntheses or guidelines pooled it, 44 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. Article
  6. Review
  7. Hepatic CBP/p300 Orchestrate Amino Acid-Driven Gluconeogenesis through Histone Crotonylation.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. The Power of Drosophila in Modeling Cancer Cachexia.Advances in experimental medicine and biology · 2025
    Review
  14. Study on the Mechanism of the Leaves ofCombinatorial chemistry & high throughput screening · 2025
    Article
  15. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors at 3 institutions in 1 country.

Pierre-Alexandre Just *Université de Paris, Institut Cochin, INSERM, CNRS, F75014, Paris, France.
Sara Charawi *Université de Paris, Institut Cochin, INSERM, CNRS, F75014, Paris, France.
Raphaël G P DenisUnité de Biologie Fonctionnelle et Adaptative, Centre National la Recherche Scientifique, Unité Mixte de Recherche 8251, Université Paris Diderot, Sorbonne Paris Cité, 75205, Paris, France.ORCID http://orcid.org/0000-0002-7677-7460
Mathilde SavallUniversité de Paris, Institut Cochin, INSERM, CNRS, F75014, Paris, France.
Massiré TraoreUniversité de Paris, Institut Cochin, INSERM, CNRS, F75014, Paris, France.
Marc ForetzUniversité de Paris, Institut Cochin, INSERM, CNRS, F75014, Paris, France.ORCID http://orcid.org/0000-0001-7017-9032
Sultan BastuUniversité de Paris, Institut Cochin, INSERM, CNRS, F75014, Paris, France.
Salimata MagassaEA4466, PRETRAM, Université Paris Descartes, Paris, France.
Nadia SenniUniversité de Paris, Institut Cochin, INSERM, CNRS, F75014, Paris, France.
Pierre SohierUniversité de Paris, Institut Cochin, INSERM, CNRS, F75014, Paris, France.
Maud WursmerUniversité de Paris, Institut Cochin, INSERM, CNRS, F75014, Paris, France.
Mireille Vasseur-CognetUMR IRD 242, UPEC, CNRS 7618, UPMC 113, INRA 1392, Sorbonne Universités Paris and Institut d'Ecologie et des Sciences de l'Environnement de Paris, Bondy, France.
Alain SchmittUniversité de Paris, Institut Cochin, INSERM, CNRS, F75014, Paris, France.
Morgane Le GallUniversité de Paris, Institut Cochin, INSERM, CNRS, F75014, Paris, France.
Marjorie LeducUniversité de Paris, Institut Cochin, INSERM, CNRS, F75014, Paris, France.
François GuillonneauUniversité de Paris, Institut Cochin, INSERM, CNRS, F75014, Paris, France.ORCID http://orcid.org/0000-0003-1484-4696
Jean-Pascal De BandtEA4466, PRETRAM, Université Paris Descartes, Paris, France.
Patrick MayeuxUniversité de Paris, Institut Cochin, INSERM, CNRS, F75014, Paris, France.
Béatrice RomagnoloUniversité de Paris, Institut Cochin, INSERM, CNRS, F75014, Paris, France.
Serge LuquetUnité de Biologie Fonctionnelle et Adaptative, Centre National la Recherche Scientifique, Unité Mixte de Recherche 8251, Université Paris Diderot, Sorbonne Paris Cité, 75205, Paris, France.
Pascale BossardUniversité de Paris, Institut Cochin, INSERM, CNRS, F75014, Paris, France.
Christine PerretUniversité de Paris, Institut Cochin, INSERM, CNRS, F75014, Paris, France. christine.perret@inserm.fr.ORCID http://orcid.org/0000-0003-4710-7051
Centre National de la Recherche Scientifique · FRDélégation Paris 5 · FRDélégation Paris 7 · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Excessive glucose production by the liver is a key factor in the hyperglycemia observed in type 2 diabetes mellitus (T2DM). Here, we highlight a novel role of liver kinase B1 (Lkb1) in this regulation. We show that mice with a hepatocyte-specific deletion of Lkb1 have higher levels of hepatic amino acid catabolism, driving gluconeogenesis. This effect is observed during both fasting and the postprandial period, identifying Lkb1 as a critical suppressor of postprandial hepatic gluconeogenesis. Hepatic Lkb1 deletion is associated with major changes in whole-body metabolism, leading to a lower lean body mass and, in the longer term, sarcopenia and cachexia, as a consequence of the diversion of amino acids to liver metabolism at the expense of muscle. Using genetic, proteomic and pharmacological approaches, we identify the aminotransferases and specifically Agxt as effectors of the suppressor function of Lkb1 in amino acid-driven gluconeogenesis.

Indexed as

Amino AcidsAMP-Activated Protein KinasesAnimalsCachexiaDiabetes Mellitus, Type 2FastingFemaleGluconeogenesisGlucoseHepatocytesHyperglycemiaLiverMaleMiceMice, KnockoutProtein Serine-Threonine KinasesAlanine-glyoxylate transaminaseAmino AcidsAMP-Activated Protein KinasesGlucoseProtein Serine-Threonine KinasesStk11 protein, mouseTransaminases

Identifiers

PMID33257663
PMCPMC7705018
OpenAlexW3106871976

What OpenQuestion holds

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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.