Evidence map›Paper›PMID 28495406›Full record

ReviewTrends in endocrinology and metabolism: TEM2017

Nuclear Receptor Function through Genomics: Lessons from the Glucocorticoid Receptor.

Daniel M Cohen, David J Steger

Registry-linked trialAbstract readReview
In one paragraph

Review in Trends in endocrinology and metabolism: TEM, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03367663 (The Effect of Prednisone on Atherogenesis as Studied in the Macrophage Foam Cell Formation Model System.), which is not on this map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
4.0field-weighted citation impact, top 6% 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.

NCT03367663 early_phase1completednot on this mapstarted 2018, after this paper: background citation

The Effect of Prednisone on Atherogenesis as Studied in the Macrophage Foam Cell Formation Model System.

TypeinterventionalSponsorProf. Tony hayek MDRan2018 to 2018Enrolled10ConditionsAtherosclerosis, Dyslipidemias, DiabetesArmsPrednisone 20 Mg, Prednisone 40 Mg
3 · Its place in the literature

Who cites it

25 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Modelling the role of glucocorticoid receptor as mediator of endocrine responses to environmental challenge.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2024
    Article
  6. Article
  7. Article
  8. Article
  9. Transcriptional control of energy metabolism by nuclear receptors.Nature reviews. Molecular cell biology · 2022
    Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. 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

2 authors at 1 institution in 1 country.

Daniel M CohenDivision of Endocrinology, Diabetes, and Metabolism, Department of Medicine, and The Institute for Diabetes, Obesity, and Metabolism, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA 19104, USA.
David J StegerDivision of Endocrinology, Diabetes, and Metabolism, Department of Medicine, and The Institute for Diabetes, Obesity, and Metabolism, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA 19104, USA. Electronic address: stegerdj@mail.med.upenn.edu.
University of Pennsylvania · US

Funding

Transcriptional and epigenomic control of adipose tissue development and functionR01DK098542 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI STEGER, DAVID J. · 2013 to 2017
$1.7M
NIDDK NIH HHS R01 DK098542
6 · The paper itself

Abstract

Unlocking the therapeutic potential of the glucocorticoid receptor (GR) has motivated a search for small molecules that selectively modulate its ability to activate or repress gene transcription. Recently, breakthrough studies in the field of genomics have reinvigorated debate over longstanding transcriptional models explaining how GR controls tissue-specific gene expression. Here, we highlight these genomic studies with the dual goals of advancing understanding of nuclear receptor-mediated transcription and stimulating thought on the development of anti-inflammatory and immunosuppressive ligands for GR that have reduced harmful effects on metabolism.

Indexed as

Gene Expression RegulationAnimalsGenomicsHumansReceptors, Cytoplasmic and NuclearReceptors, GlucocorticoidTranscriptional ActivationTranscription FactorsReceptors, Cytoplasmic and NuclearReceptors, GlucocorticoidTranscription Factorscistromicsfunctional genomicsglucocorticoid receptornuclear receptortranscription

Identifiers

PMID28495406
PMCPMC5505657
OpenAlexW2612699908

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.