Evidence map›Paper›PMID 25476896›Full record

ArticleCell death & disease2014

Role of non-genomic androgen signalling in suppressing proliferation of fibroblasts and fibrosarcoma cells.

G Castoria, P Giovannelli, M Di Donato, A Ciociola, R Hayashi, F Bernal, E Appella, F Auricchio, A Migliaccio

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

34 citing papers in PubMed, 48 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

9 authors at 2 institutions in 2 countries.

G CastoriaDepartment of Biochemistry, Biophysics and General Pathology-II University of Naples, Via L. De Crecchio 7, 80138 Naples, Italy.
P GiovannelliDepartment of Biochemistry, Biophysics and General Pathology-II University of Naples, Via L. De Crecchio 7, 80138 Naples, Italy.
M Di DonatoDepartment of Biochemistry, Biophysics and General Pathology-II University of Naples, Via L. De Crecchio 7, 80138 Naples, Italy.
A CiociolaDepartment of Biochemistry, Biophysics and General Pathology-II University of Naples, Via L. De Crecchio 7, 80138 Naples, Italy.
R HayashiLaboratory of Cell Biology, National Cancer Institute, Bethesda, MD 20892-4256, USA.
F BernalMetabolism Branch, National Cancer Institute, Bethesda, MD 20892-4256, USA.
E AppellaLaboratory of Cell Biology, National Cancer Institute, Bethesda, MD 20892-4256, USA.
F AuricchioDepartment of Biochemistry, Biophysics and General Pathology-II University of Naples, Via L. De Crecchio 7, 80138 Naples, Italy.
A MigliaccioDepartment of Biochemistry, Biophysics and General Pathology-II University of Naples, Via L. De Crecchio 7, 80138 Naples, Italy.ORCID 0000000241972055
Institute of Genetics and Biophysics · ITNational Cancer Institute · US

Funding

Molecule-Guided Investigations into p53 BiologyZIABC011261 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI BERNAL, FEDERICO · 2010 to 2014
$1.5M
Intramural NIH HHS ZIA BC011261
6 · The paper itself

Abstract

The functions of androgen receptor (AR) in stromal cells are still debated in spite of the demonstrated importance of these cells in organ development and diseases. Here, we show that physiological androgen concentration (10 nM R1881 or DHT) fails to induce DNA synthesis, while it consistently stimulates cell migration in mesenchymal and transformed mesenchymal cells. Ten nanomolar R1881 triggers p27 Ser10 phosphorylation and its stabilization in NIH3T3 fibroblasts. Activation of Rac and its downstream effector DYRK 1B is responsible for p27 Ser10 phosphorylation and cell quiescence. Ten nanomolar androgen also inhibits transformation induced by oncogenic Ras in NIH3T3 fibroblasts. Overexpression of an AR mutant unable to interact with filamin A, use of a small peptide displacing AR/filamin A interaction, and filamin A knockdown indicate that the androgen-triggered AR/filamin A complex regulates the pathway leading to p27 Ser10 phosphorylation and cell cycle arrest. As the AR/filamin A complex is also responsible for migration stimulated by 10 nM androgen, our report shows that the androgen-triggered AR/filamin A complex controls, through Rac 1, the decision of cells to halt cell cycle and migration. This study reveals a new and unexpected role of androgen/AR signalling in coordinating stromal cell functions.

Indexed as

Signal TransductionAnimalsCell Cycle CheckpointsCell MovementCell ProliferationCyclin-Dependent Kinase Inhibitor p27DihydrotestosteroneDyrk KinasesFibroblastsFibrosarcomaFilaminsGene Expression RegulationHumansMaleMesenchymal Stem CellsMetriboloneAR protein, humanCDKN1B protein, humanCyclin-Dependent Kinase Inhibitor p27DihydrotestosteroneDyrk KinasesFilaminsMetriboloneProtein Serine-Threonine KinasesProtein-Tyrosine Kinasesrac1 GTP-Binding ProteinRAC1 protein, humanras ProteinsReceptors, AndrogenSerineTestosterone Congeners

Identifiers

PMID25476896
PMCPMC4649827
OpenAlexW2077156803

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.