Evidence map›Paper›PMID 31789593›Full record

ArticleeLife2019

Modulating FOXO3 transcriptional activity by small, DBD-binding molecules.

Judith Hagenbuchner, Veronika Obsilova, Teresa Kaserer, Nora Kaiser, Bettina Rass, Katarina Psenakova, Vojtech Docekal, Miroslava Alblova, Klara Kohoutova, Daniela Schuster and 5 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

10 citing papers in PubMed, 17 citations in OpenAlex.

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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

15 authors at 4 institutions in 2 countries.

Judith Hagenbuchner *Department of Pediatrics II, Medical University Innsbruck, Innsbruck, Austria.ORCID 0000-0003-1396-3407
Veronika Obsilova *Department of Structural Biology of Signaling Proteins, Institute of Physiology, Division BIOCEV, The Czech Academy of Sciences, Prague, Czech Republic.ORCID 0000-0003-4887-0323
Teresa Kaserer *Pharmaceutical Chemistry, Institute of Pharmacy, University of Innsbruck, Innsbruck, Austria.ORCID 0000-0003-0372-1885
Nora KaiserDepartment of Pediatrics I, Medical University Innsbruck, Innsbruck, Austria.
Bettina RassDepartment of Pediatrics I, Medical University Innsbruck, Innsbruck, Austria.
Katarina PsenakovaDepartment of Structural Biology of Signaling Proteins, Institute of Physiology, Division BIOCEV, The Czech Academy of Sciences, Prague, Czech Republic.ORCID 0000-0001-8877-6599
Vojtech DocekalDepartment of Organic Chemistry, Faculty of Science, Charles University, Prague, Czech Republic.
Miroslava AlblovaDepartment of Structural Biology of Signaling Proteins, Institute of Physiology, Division BIOCEV, The Czech Academy of Sciences, Prague, Czech Republic.
Klara KohoutovaDepartment of Structural Biology of Signaling Proteins, Institute of Physiology, Division BIOCEV, The Czech Academy of Sciences, Prague, Czech Republic.
Daniela SchusterPharmaceutical Chemistry, Institute of Pharmacy, University of Innsbruck, Innsbruck, Austria.
Tatsiana AneichykDivision of Molecular Pathophysiology, Biocenter, Medical University Innsbruck, Innsbruck, Austria.
Jan VeselyDepartment of Organic Chemistry, Faculty of Science, Charles University, Prague, Czech Republic.
Petra ObexerDepartment of Pediatrics II, Medical University Innsbruck, Innsbruck, Austria.
Tomas ObsilDepartment of Structural Biology of Signaling Proteins, Institute of Physiology, Division BIOCEV, The Czech Academy of Sciences, Prague, Czech Republic.ORCID 0000-0003-4602-1272
Michael J AusserlechnerDepartment of Pediatrics I, Medical University Innsbruck, Innsbruck, Austria.ORCID 0000-0002-1015-2302
Innsbruck Medical University · ATCzech Academy of Sciences · CZCharles University · CZUniversität Innsbruck · AT

Funding

Austrian Science Fund I3089-B28Austrian Science Fund FWF I 3089Grantová Agentura České Republiky 17-33854L
6 · The paper itself

Abstract

FOXO transcription factors are critical regulators of cell homeostasis and steer cell death, differentiation and longevity in mammalian cells. By combined pharmacophore-modeling-based in silico and fluorescence polarization-based screening we identified small molecules that physically interact with the DNA-binding domain (DBD) of FOXO3 and modulate the FOXO3 transcriptional program in human cells. The mode of interaction between compounds and the FOXO3-DBD was assessed

Indexed as

Binding SitesCell Line, TumorDNAForkhead Box Protein O3Gene Expression ProfilingGene Knockdown TechniquesHEK293 CellsHumansMagnetic Resonance SpectroscopyModels, MolecularMolecular Docking SimulationNucleic Acid ConformationPromoter Regions, GeneticProtein BindingProtein DomainsSmall Molecule LibrariesDNAForkhead Box Protein O3FOXO3 protein, humanSmall Molecule Librariesbiochemistrycancer biologychemical biologydockingdrug targetingFOXO transcription factorshumanmolecular biophysicspharmacophore modellingsmall compoundsstructural biology

Identifiers

PMID31789593
PMCPMC6919977
OpenAlexW2989961232

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.