Evidence map›Paper›PMID 23637875›Full record

ArticlePloS one2013

Genetic, functional and molecular features of glucocorticoid receptor binding.

Francesca Luca, Joseph C Maranville, Allison L Richards, David B Witonsky, Matthew Stephens, Anna Di Rienzo

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.2field-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

13 citing papers in PubMed, 26 citations in OpenAlex.

  1. The Bidirectional Interaction Between NF-Journal of immunology research · 2025
    Review
  2. Review
  3. Social status alters chromatin accessibility and the gene regulatory response to glucocorticoid stimulation in rhesus macaques.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  4. Review
  5. Facilitating Analysis of Publicly Available ChIP-Seq Data for Integrative Studies.AMIA ... Annual Symposium proceedings. AMIA Symposium · 2019
    Article
  6. Rosiglitazone, a Ligand to PPARPPAR research · 2019
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. 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

6 authors at 1 institution in 1 country.

Francesca LucaDepartment of Human Genetics, University of Chicago, Chicago, Illinois, United States of America.
Joseph C Maranville
Allison L Richards
David B Witonsky
Matthew Stephens
Anna Di Rienzo
University of Chicago · US

Funding

POPULATION AND EVOLUTIONARY GENETICS OF NIDDMIR01DK056670 · NIDDK · UNIVERSITY OF CHICAGO · PI DI RIENZO, ANNA · 2001 to 2010
$3.2M
NIDDK NIH HHS NIH R01DK056670NIDDK NIH HHS NIH R01DK056670-S1NIDDK NIH HHS R01 DK056670
6 · The paper itself

Abstract

Glucocorticoids (GCs) are key mediators of stress response and are widely used as pharmacological agents to treat immune diseases, such as asthma and inflammatory bowel disease, and certain types of cancer. GCs act mainly by activating the GC receptor (GR), which interacts with other transcription factors to regulate gene expression. Here, we combined different functional genomics approaches to gain molecular insights into the mechanisms of action of GC. By profiling the transcriptional response to GC over time in 4 Yoruba (YRI) and 4 Tuscans (TSI) lymphoblastoid cell lines (LCLs), we suggest that the transcriptional response to GC is variable not only in time, but also in direction (positive or negative) depending on the presence of specific interacting transcription factors. Accordingly, when we performed ChIP-seq for GR and NF-κB in two YRI LCLs treated with GC or with vehicle control, we observed that features of GR binding sites differ for up- and down-regulated genes. Finally, we show that eQTLs that affect expression patterns only in the presence of GC are 1.9-fold more likely to occur in GR binding sites, compared to eQTLs that affect expression only in its absence. Our results indicate that genetic variation at GR and interacting transcription factors binding sites influences variability in gene expression, and attest to the power of combining different functional genomic approaches.

Indexed as

Anti-Inflammatory AgentsCell LineGene Expression RegulationGlucocorticoidsHumansNF-kappa BProtein BindingQuantitative Trait LociReceptors, GlucocorticoidTranscriptomeAnti-Inflammatory AgentsGlucocorticoidsNF-kappa BReceptors, Glucocorticoid

Identifiers

PMID23637875
PMCPMC3640037
OpenAlexW2053522743

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.