Evidence map›Paper›PMID 27362806›Full record

ArticleCell death & disease2016

MDM2 facilitates adipocyte differentiation through CRTC-mediated activation of STAT3.

P Hallenborg, M Siersbæk, I Barrio-Hernandez, R Nielsen, K Kristiansen, S Mandrup, L Grøntved, B Blagoev

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.6field-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

20 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
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  17. Function and Transcriptional Regulation of BovineInternational journal of molecular sciences · 2019
    Article
  18. Review
  19. p53 Functions in Adipose Tissue Metabolism and Homeostasis.International journal of molecular sciences · 2018
    Review
  20. 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

8 authors at 2 institutions in 1 country.

P HallenborgDepartment of Biochemistry and Molecular Biology, University of Southern Denmark, Odense M, Denmark.
M SiersbækDepartment of Biochemistry and Molecular Biology, University of Southern Denmark, Odense M, Denmark.
I Barrio-HernandezDepartment of Biochemistry and Molecular Biology, University of Southern Denmark, Odense M, Denmark.
R NielsenDepartment of Biochemistry and Molecular Biology, University of Southern Denmark, Odense M, Denmark.
K KristiansenDepartment of Biology, University of Copenhagen, Copenhagen N, Denmark.
S MandrupDepartment of Biochemistry and Molecular Biology, University of Southern Denmark, Odense M, Denmark.ORCID 0000-0002-0961-5787
L GrøntvedDepartment of Biochemistry and Molecular Biology, University of Southern Denmark, Odense M, Denmark.
B BlagoevDepartment of Biochemistry and Molecular Biology, University of Southern Denmark, Odense M, Denmark.
University of Southern Denmark · DKUniversity of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ubiquitin ligase MDM2 is best known for balancing the activity of the tumor suppressor p53. We have previously shown that MDM2 is vital for adipocyte conversion through controlling Cebpd expression in a p53-independent manner. Here, we show that the proadipogenic effect of MDM2 relies on activation of the STAT family of transcription factors. Their activation was required for the cAMP-mediated induction of target genes. Interestingly, rather than influencing all cAMP-stimulated genes, inhibition of the kinases directly responsible for STAT activation, namely JAKs, or ablation of MDM2, each resulted in abolished induction of a subset of cAMP-stimulated genes, with Cebpd being among the most affected. Moreover, STATs were able to interact with the transcriptional cofactors CRTC2 and CRTC3, hitherto only reported to associate with the cAMP-responsive transcription factor CREB. Last but not least, the binding of CRTC2 to a transcriptional enhancer that interacts with the Cebpd promoter was dramatically decreased upon JAK inhibition. Our data reveal the existence of an unusual functional interplay between STATs and CREB at the onset of adipogenesis through shared CRTC cofactors.

Indexed as

Cell DifferentiationAdipocytesAnimalsCCAAT-Enhancer-Binding Protein-deltaChromatinCyclic AMPGene Knockdown TechniquesImidazolesJanus KinasesMiceModels, BiologicalPiperazinesProtein BindingProto-Oncogene Proteins c-mdm2STAT3 Transcription FactorTranscription FactorsCCAAT-Enhancer-Binding Protein-deltaCebpd protein, mouseChromatinCrtc2 protein, mouseCRTC3 protein, mouseCyclic AMPImidazolesJanus Kinasesnutlin 3PiperazinesProto-Oncogene Proteins c-mdm2STAT3 Transcription FactorTranscription FactorsTumor Suppressor Protein p53

Identifiers

PMID27362806
PMCPMC5108339
OpenAlexW2460374461

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.