Evidence map›Paper›PMID 25053585›Full record

ArticleDiabetes2015

Deleted in breast cancer 1 limits adipose tissue fat accumulation and plays a key role in the development of metabolic syndrome phenotype.

Carlos Escande, Veronica Nin, Tamar Pirtskhalava, Claudia C S Chini, Tamar Tchkonia, James L Kirkland, Eduardo N Chini

Open access · greenAbstract read
In one paragraph

Article in Diabetes, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

17 citing papers in PubMed, 24 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Genetic variants inFrontiers in genetics · 2024
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Loss of DBC1 (CCAR2) affects TNFα-induced lipolysis andJournal of molecular endocrinology · 2018
    Article
  15. Potential Modulation of Sirtuins by Oxidative Stress.Oxidative medicine and cellular longevity · 2016
    Review
  16. Vascular repair strategies in type 2 diabetes: novel insights.Cardiovascular diagnosis and therapy · 2015
    Review
  17. 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

7 authors at 2 institutions in 2 countries.

Carlos EscandeKogod Aging Center, Mayo Clinic, Rochester, MN Department of Anesthesiology, Mayo Clinic, Rochester, MN Institut Pasteur Montevideo, Montevideo, Uruguay.
Veronica NinKogod Aging Center, Mayo Clinic, Rochester, MN Department of Anesthesiology, Mayo Clinic, Rochester, MN.
Tamar PirtskhalavaKogod Aging Center, Mayo Clinic, Rochester, MN.
Claudia C S ChiniKogod Aging Center, Mayo Clinic, Rochester, MN Department of Anesthesiology, Mayo Clinic, Rochester, MN.
Tamar TchkoniaKogod Aging Center, Mayo Clinic, Rochester, MN.
James L KirklandKogod Aging Center, Mayo Clinic, Rochester, MN.
Eduardo N ChiniKogod Aging Center, Mayo Clinic, Rochester, MN Department of Anesthesiology, Mayo Clinic, Rochester, MN chini.eduardo@mayo.edu.
Mayo Clinic · USWinnMed · US

Funding

Mayo Clinic Center for Translational Science ActivitiesUL1TR000135 · NCATS · MAYO CLINIC ROCHESTER · PI KHOSLA, SUNDEEP · 2012 to 2015
$41.2M
Systems Biology and Bioinformatics CoreP01AG041122 · NIA · MAYO CLINIC ROCHESTER · PI CAMPISI, JUDITH · 2012 to 2016
$9.8M
Effect of Aging on Preadipocyte DifferentiationR37AG013925 · NIA · MAYO CLINIC ROCHESTER · PI KIRKLAND, JAMES L. · 2016 to 2025
$6.6M
The Sir2-p53-IGF Link in Mammalian Life-Span ControlR01AG026094 · NIA · UNIVERSITY OF VIRGINIA · PI CHINI, EDUARDO N · 2006 to 2016
$3.8M
Effect of Aging on Preadipocyte DifferentiationR01AG013925 · NIA · MAYO CLINIC ROCHESTER · PI KIRKLAND, JAMES L. · 1997 to 2012
$3.7M
Molecular mechanisms of fatty liver disease: role of the protein DBC1R01DK084055 · NIDDK · MAYO CLINIC ROCHESTER · PI CHINI, EDUARDO N · 2009 to 2013
$1.5M
NCATS NIH HHS UL1 TR000135NIA NIH HHS AG-13925NIA NIH HHS AG-41122NIA NIH HHS P01 AG041122NIA NIH HHS R01 AG013925NIA NIH HHS R01 AG026094NIDDK NIH HHS DK-084055NIDDK NIH HHS R01 DK084055
6 · The paper itself

Abstract

Obesity is often regarded as the primary cause of metabolic syndrome. However, many lines of evidence suggest that obesity may develop as a protective mechanism against tissue damage during caloric surplus and that it is only when the maximum fat accumulation capacity is reached and fatty acid spillover occurs into to peripheral tissues that metabolic diseases develop. In this regard, identifying the molecular mechanisms that modulate adipocyte fat accumulation and fatty acid spillover is imperative. Here we identify the deleted in breast cancer 1 (DBC1) protein as a key regulator of fat storage capacity of adipocytes. We found that knockout (KO) of DBC1 facilitated fat cell differentiation and lipid accumulation and increased fat storage capacity of adipocytes in vitro and in vivo. This effect resulted in a "healthy obesity" phenotype. DBC1 KO mice fed a high-fat diet, although obese, remained insulin sensitive, had lower free fatty acid in plasma, were protected against atherosclerosis and liver steatosis, and lived longer. We propose that DBC1 is part of the molecular machinery that regulates fat storage capacity in adipocytes and participates in the "turn-off" switch that limits adipocyte fat accumulation and leads to fat spillover into peripheral tissues, leading to the deleterious effects of caloric surplus.

Indexed as

Adaptor Proteins, Signal TransducingAdipocytesAnimalsAortaAtherosclerosisCell DifferentiationCells, CulturedEndothelial CellsFatty Acids, NonesterifiedFatty LiverFemaleGlycerolHumansMetabolic SyndromeMice, KnockoutObesityAdaptor Proteins, Signal TransducingCCAR2 protein, humanFatty Acids, NonesterifiedGlycerolKIAA1967 protein, mouseSIRT1 protein, humanSirt1 protein, mouseSirtuin 1

Identifiers

PMID25053585
PMCPMC4274806
OpenAlexW2125485188

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.