Evidence map›Paper›PMID 23393188›Full record

ArticleNucleic acids research2013

Genome-wide analysis of LXRα activation reveals new transcriptional networks in human atherosclerotic foam cells.

Radmila Feldmann, Cornelius Fischer, Vitam Kodelja, Sarah Behrens, Stefan Haas, Martin Vingron, Bernd Timmermann, Anne Geikowski, Sascha Sauer

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
4.6field-weighted citation impact, top 5% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Integrative analysis reveals multiple modes of LXR transcriptional regulation in liver.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  6. Nuclear Receptors and Lipid Sensing.Advances in experimental medicine and biology · 2022
    Article
  7. Review
  8. Motif grammar: The basis of the language of gene expression.Computational and structural biotechnology journal · 2020
    Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Transcriptional regulation of hepatic lipogenesis.Nature reviews. Molecular cell biology · 2015
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
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

9 authors at 2 institutions in 1 country.

Radmila FeldmannMax Planck Institute for Molecular Genetics, Ihnestraße 63-73, 14195 Berlin, Germany.
Cornelius Fischer
Vitam Kodelja
Sarah Behrens
Stefan Haas
Martin Vingron
Bernd Timmermann
Anne Geikowski
Sascha Sauer
Freie Universität Berlin · DEMax Planck Institute for Molecular Genetics · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Increased physiological levels of oxysterols are major risk factors for developing atherosclerosis and cardiovascular disease. Lipid-loaded macrophages, termed foam cells, are important during the early development of atherosclerotic plaques. To pursue the hypothesis that ligand-based modulation of the nuclear receptor LXRα is crucial for cell homeostasis during atherosclerotic processes, we analysed genome-wide the action of LXRα in foam cells and macrophages. By integrating chromatin immunoprecipitation-sequencing (ChIP-seq) and gene expression profile analyses, we generated a highly stringent set of 186 LXRα target genes. Treatment with the nanomolar-binding ligand T0901317 and subsequent auto-regulatory LXRα activation resulted in sequence-dependent sharpening of the genome-binding patterns of LXRα. LXRα-binding loci that correlated with differential gene expression revealed 32 novel target genes with potential beneficial effects, which in part explained the implications of disease-associated genetic variation data. These observations identified highly integrated LXRα ligand-dependent transcriptional networks, including the APOE/C1/C4/C2-gene cluster, which contribute to the reversal of cholesterol efflux and the dampening of inflammation processes in foam cells to prevent atherogenesis.

Indexed as

Gene Regulatory NetworksApoptosisAtherosclerosisBenzenesulfonamidesCell LineCells, CulturedCholesterolFluorocarbonsFoam CellsGene Expression RegulationGenetic LociGenetic VariationGenome, HumanHumansHydrocarbons, FluorinatedLigandsBenzenesulfonamidesCholesterolFluorocarbonsHydrocarbons, FluorinatedLigandsLiver X ReceptorsNR1H3 protein, humanOrphan Nuclear ReceptorsPPAR alphaSulfonamidesT0901317

Identifiers

PMID23393188
PMCPMC3616743
OpenAlexW2151659157

What OpenQuestion holds

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LicenceCC BY-NC
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.