Evidence map›Paper›PMID 24415752›Full record

ArticleThe Journal of biological chemistry2014

Deleted in breast cancer 1 (DBC1) protein regulates hepatic gluconeogenesis.

Veronica Nin, Claudia C S Chini, Carlos Escande, Verena Capellini, Eduardo N Chini

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

12 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. PROX1-mediated epigenetic silencing ofInternational journal of biological sciences · 2023
    Article
  5. Article
  6. DBC1, p300, HDAC3, and Siah1 coordinately regulate ELL stability and function for expression of its target genes.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  7. Article
  8. Loss of DBC1 (CCAR2) affects TNFα-induced lipolysis andJournal of molecular endocrinology · 2018
    Article
  9. Article
  10. Augmentation of histone deacetylase 3 (Clinical epigenetics · 2016
    Article
  11. Article
  12. 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

5 authors at 2 institutions in 1 country.

Veronica NinFrom the Department of Anesthesiology and Kogod Center on Aging, Mayo Clinic, Rochester, Minnesota 55905.
Claudia C S Chini
Carlos Escande
Verena Capellini
Eduardo N Chini
Mayo Clinic · USWinnMed · US

Funding

Obesity and Energy Metabolism CoreP30DK050456 · NIDDK · UNIVERSITY OF MINNESOTA TWIN CITIES · PI BERNLOHR, DAVID A · 1995 to 2015
$17.0M
Molecular mechanisms of fatty liver disease: role of the protein DBC1R01DK084055 · NIDDK · MAYO CLINIC ROCHESTER · PI CHINI, EDUARDO N · 2009 to 2013
$1.5M
NIDDK NIH HHS DK-084055NIDDK NIH HHS P30 DK050456NIDDK NIH HHS R01 DK084055
6 · The paper itself

Abstract

Liver gluconeogenesis is essential to provide energy to glycolytic tissues during fasting periods. However, aberrant up-regulation of this metabolic pathway contributes to the progression of glucose intolerance in individuals with diabetes. Phosphoenolpyruvate carboxykinase (PEPCK) expression plays a critical role in the modulation of gluconeogenesis. Several pathways contribute to the regulation of PEPCK, including the nuclear receptor Rev-erbα and the histone deacetylase SIRT1. Deleted in breast cancer 1 (DBC1) is a nuclear protein that binds to and regulates both Rev-erbα and SIRT1 and, therefore, is a candidate to participate in the regulation of PEPCK. In this work, we provide evidence that DBC1 regulates glucose metabolism and the expression of PEPCK. We show that DBC1 levels decrease early in the fasting state. Also, DBC1 KO mice display higher gluconeogenesis in a normal and a high-fat diet. DBC1 absence leads to an increase in PEPCK mRNA and protein expression. Conversely, overexpression of DBC1 results in a decrease in PEPCK mRNA and protein levels. DBC1 regulates the levels of Rev-erbα, and manipulation of Rev-erbα activity or levels prevents the effect of DBC1 on PEPCK. In addition, Rev-erbα levels decrease in the first hours of fasting. Finally, knockdown of the deacetylase SIRT1 eliminates the effect of DBC1 knockdown on Rev-erbα levels and PEPCK expression, suggesting that the mechanism of PEPCK regulation is, at least in part, dependent on the activity of this enzyme. Our results point to DBC1 as a novel regulator of gluconeogenesis.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsDietary FatsFastingGene Expression Regulation, EnzymologicGluconeogenesisGlucoseHep G2 CellsHumansLiverMiceMice, KnockoutNuclear Receptor Subfamily 1, Group D, Member 1Phosphoenolpyruvate Carboxykinase (ATP)Sirtuin 1Adaptor Proteins, Signal TransducingCCAR2 protein, humanDietary FatsGlucoseNR1D1 protein, humanNr1d1 protein, mouseNuclear Receptor Subfamily 1, Group D, Member 1Phosphoenolpyruvate Carboxykinase (ATP)SIRT1 protein, humanSirt1 protein, mouseSirtuin 1Deleted In Breast Cancer 1GluconeogenesisMetabolismNuclear ReceptorsRev-erbαSignal TransductionSIRT1

Identifiers

PMID24415752
PMCPMC3937628
OpenAlexW2006756337

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.