Evidence map›Paper›PMID 23885094›Full record

ArticleMolecular endocrinology (Baltimore, Md.)2013

Negative regulation of estrogen signaling by ERβ and RIP140 in ovarian cancer cells.

Aurélie Docquier, Aurélie Garcia, Julien Savatier, Abdel Boulahtouf, Sandrine Bonnet, Virginie Bellet, Muriel Busson, Emmanuel Margeat, Stéphan Jalaguier, Cathy Royer and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular endocrinology (Baltimore, Md.), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

27 citing papers in PubMed, 41 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

12 authors at 4 institutions in 1 country.

Aurélie DocquierInstitut de Recherche en Cancérologie de Montpellier, INSERM, U896, Montpellier F-34298, France.
Aurélie Garcia
Julien Savatier
Abdel Boulahtouf
Sandrine Bonnet
Virginie Bellet
Muriel Busson
Emmanuel Margeat
Stéphan Jalaguier
Cathy Royer
Patrick Balaguer
Vincent Cavaillès
Inserm · FRInstitut de Recherche en Cancérologie de Montpellier · FRUniversité de Montpellier · FRCentre de Biologie Structurale · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In hormone-dependent tissues such as breast and ovary, tumorigenesis is associated with an altered expression ratio between the two estrogen receptor (ER) subtypes. In this study, we investigated the effects of ERβ ectopic expression on 17β-estradiol (E2)-induced transactivation and cell proliferation in ERα-positive BG1 ovarian cancer cells. As expected, ERβ expression strongly decreased the mitogenic effect of E2, significantly reduced E2-dependent transcriptional responses (both on a stably integrated estrogen response element [ERE] reporter gene and on E2-induced mRNAs), and strongly enhanced the formation of ER heterodimers as evidenced by chromatin immunoprecipitation analysis. Inhibition by the ERα-selective ligand propyl pyrazole triol was less marked than with the pan-agonist (E2) or the ERβ-selective (8β-vinyl-estradiol) ligands, indicating that ERβ activation reinforced the inhibitory effects of ERβ. Interestingly, in E2-stimulated BG1 cells, ERβ was more efficient than ERα to regulate the expression of receptor-interacting protein 140 (RIP140), a major ERα transcriptional corepressor. In addition, we found that the RIP140 protein interacted better with ERβ than with ERα (both in vitro and in intact cells by fluorescence cross-correlation spectroscopy). Moreover, RIP140 recruitment on the stably integrated reporter ERE was increased upon ERβ overexpression, and ERβ activity was more sensitive to repression by RIP140. Finally, small interfering RNA-mediated knockdown of RIP140 expression abolished the repressive effect exerted by activated ERβ on the regulation of ERE-controlled transcription by estrogens. Altogether, these data demonstrate the inhibitory effects of ERβ on estrogen signaling in ovarian cancer cells and the key role that RIP140 plays in this phenomenon.

Indexed as

Signal TransductionAdaptor Proteins, Signal TransducingAnimalsCell Line, TumorCell ProliferationChlorocebus aethiopsCOS CellsDNA, NeoplasmEstrogen Receptor alphaEstrogen Receptor betaEstrogensFemaleGene Expression Regulation, NeoplasticGenes, ReporterHumansLigandsAdaptor Proteins, Signal TransducingDNA, NeoplasmESR1 protein, humanEstrogen Receptor alphaEstrogen Receptor betaEstrogensLigandsNRIP1 protein, humanNuclear ProteinsNuclear Receptor Interacting Protein 1

Identifiers

PMID23885094
PMCPMC5415230
OpenAlexW2086709329

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.