Evidence map›Paper›PMID 28868790›Full record

ReviewAnnals of the New York Academy of Sciences2018

Insulin regulation of gluconeogenesis.

Maximilian Hatting, Clint D J Tavares, Kfir Sharabi, Amy K Rines, Pere Puigserver

Registry-linked trialOpen access · bronzeAbstract readReview
In one paragraph

Review in Annals of the New York Academy of Sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04810572 (Evaluation of the Effects of a Nutraceutical Composition Containing Derivatives From Natural Products on the Modulation of the Endocrine Neuroimmune Axis - Translational Study.), which is not on this map. Cited by 277 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
277citing papers in PubMed, 3 pooled it
10.5field-weighted citation impact, top 1% 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.

NCT04810572 nacompletednot on this mapstarted 2021, after this paper: background citation

Evaluation of the Effects of a Nutraceutical Composition Containing Derivatives From Natural Products on the Modulation of the Endocrine Neuroimmune Axis - Translational Study.

TypeinterventionalSponsorUniversity of Sao Paulo General HospitalRan2021 to 2022Enrolled162ConditionsInsulin Resistance, Inflammatory Bowel Diseases, Overweight and Obesity, HealthyArmsComposition with Silymarin, Low-mineral composition without Silymarin
3 · Its place in the literature

Who cites it

277 citing papers in PubMed, 3 syntheses or guidelines pooled it, 563 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. A Systematic Review ofMolecules (Basel, Switzerland) · 2022
    Pooled it
  4. Trial
  5. Effects ofGut microbes · 2026
    Article
  6. Article
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  11. Antidiabetic Properties ofLife (Basel, Switzerland) · 2026
    Review
  12. A FOXO1-G6PC transcriptional axis restrains renal cell carcinoma progression: multi-omics, epigenetic, and mechanistic evidence.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Article
  13. Article
  14. Review
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217 more citing papers are in PubMed but not listed here.

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

5 authors at 3 institutions in 1 country.

Maximilian HattingDepartment of Cancer Biology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Clint D J TavaresDepartment of Cancer Biology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Kfir SharabiDepartment of Cancer Biology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Amy K RinesDepartment of Cancer Biology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Pere PuigserverDepartment of Cancer Biology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Dana-Farber Cancer Institute · USHarvard University · USHarvard Stem Cell Institute · US

Funding

Chemical Biology of Mitochondria and DiabetesR24DK080261 · NIDDK · DANA-FARBER CANCER INST · PI SPIEGELMAN, BRUCE M. · 2007 to 2016
$13.9M
NIDDK NIH HHS R24 DK080261
6 · The paper itself

Abstract

The coordinated regulation between cellular glucose uptake and endogenous glucose production is indispensable for the maintenance of constant blood glucose concentrations. The liver contributes significantly to this process by altering the levels of hepatic glucose release, through controlling the processes of de novo glucose production (gluconeogenesis) and glycogen breakdown (glycogenolysis). Various nutritional and hormonal stimuli signal to alter hepatic gluconeogenic flux, and suppression of this metabolic pathway during the postprandial state can, to a significant extent, be attributed to insulin. Here, we review some of the molecular mechanisms through which insulin modulates hepatic gluconeogenesis, thus controlling glucose production by the liver to ultimately maintain normoglycemia. Various signaling pathways governed by insulin converge at the level of transcriptional regulation of the key hepatic gluconeogenic genes PCK1 and G6PC, highlighting this as one of the focal mechanisms through which gluconeogenesis is modulated. In individuals with compromised insulin signaling, such as insulin resistance in type 2 diabetes, insulin fails to suppress hepatic gluconeogenesis, even in the fed state; hence, an insight into these insulin-moderated pathways is critical for therapeutic purposes.

Indexed as

AnimalsBlood GlucoseDiabetes Mellitus, Type 2Gene Expression RegulationGluconeogenesisGlycogenolysisHomeostasisHumansHypoglycemic AgentsInsulinInsulin ResistanceLiverModels, AnimalObesityProtein KinasesSignal TransductionBlood GlucoseHypoglycemic AgentsInsulinProtein Kinasesgluconeogenesisglucoseglycogenolysisinsulinregulation

Identifiers

PMID28868790
PMCPMC5927596
OpenAlexW2753709051

What OpenQuestion holds

Textmetadata
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Read underepoch 390

Registered trials

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.