Evidence map›Paper›PMID 15805579›Full record

ArticleEndocrine2005

Androgen-receptor coregulators mediate the suppressive effect of androgen signals on vitamin D receptor activity.

Huei-Ju Ting, Bo-Ying Bao, Cheng-Lung Hsu, Yi-Fen Lee

Abstract read
PubMed Publisher
In one paragraph

Article in Endocrine, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

24 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
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  4. The Role of NCOA4-Mediated Ferritinophagy in Health and Disease.Pharmaceuticals (Basel, Switzerland) · 2018
    Review
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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

4 authors at 1 institution in 1 country.

Huei-Ju TingDepartment of Urology, University of Rochester, 601 Elmwood Ave., Rochester, NY 14642, USA.
Bo-Ying Bao
Cheng-Lung Hsu
Yi-Fen Lee
University of Rochester · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Overexpression of androgen receptors (AR) in PC-3 cell, and treatment of 5alpha-dihydrotestosterone in LNCaP cells lead to the suppression of VDR transactivation. Competition for shared coregulators between AR and VDR is one possible mechanism to explain the suppressive effect of androgen-AR signals on VDR activity. Among the AR coregulators we tested, ARA54, ARA70, supervillin, and gelsolin were found to enhance VDR transactivation. Further characterization of the interaction between ARA54 or ARA70 and VDR demonstrated a direct interaction between VDR and ARA70, but no association between ARA54 and VDR. The LXXLL motif of ARA70 is essential for interaction with VDR and partially responsible for its function as a coactivator of VDR. The suppression of VDR transactivation by AR signal was restored by overexpression of ARA70, but not ARA54. Together, ARA70 and ARA54 modulate VDR transactivation, and the competition for ARA70 mediates the suppressive effect of androgen-AR on VDR transactivation.

Indexed as

Amino Acid MotifsAnimalsCalcitriolCell Line, TumorChlorocebus aethiopsCOS CellsDNA-Binding ProteinsGelsolinGlutathione TransferaseHistone AcetyltransferasesHormone AntagonistsHumansIntracellular Signaling Peptides and ProteinsMaleMembrane ProteinsMicrofilament ProteinsCalcitriolDNA-Binding ProteinsGelsolinGlutathione TransferaseHistone AcetyltransferasesHormone AntagonistsIntracellular Signaling Peptides and ProteinsMembrane ProteinsMicrofilament ProteinsNCOA1 protein, humanNCOA4 protein, humanNCOR2 protein, humanNuclear Receptor Coactivator 1Nuclear Receptor CoactivatorsNuclear Receptor Co-Repressor 2Oncogene ProteinsReceptors, AndrogenReceptors, CalcitriolRepressor ProteinsRNF14 protein, humanSVIL protein, humanTranscription Factors

Identifiers

PMID15805579
OpenAlexW2008312359

What OpenQuestion holds

Textmetadata
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.