Evidence map›Paper›PMID 16158045›Full record

ArticleOncogene2006

ERalpha and ERbeta expression and transcriptional activity are differentially regulated by HDAC inhibitors.

V Duong, A Licznar, R Margueron, N Boulle, M Busson, M Lacroix, B S Katzenellenbogen, V Cavaillès, G Lazennec

Open access · bronzeAbstract read
In one paragraph

Article in Oncogene, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

32 citing papers in PubMed, 75 citations in OpenAlex.

  1. Article
  2. N-Myc and STAT Interactor is an Endometriosis Suppressor.International journal of molecular sciences · 2024
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  19. Article
  20. Functional genomic methods to study estrogen receptor activity.Journal of mammary gland biology and neoplasia · 2012
    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 3 institutions in 2 countries.

V DuongINSERM U540 'Molecular and Cellular Endocrinology of Cancers', 34090 Montpellier, France.
A Licznar
R Margueron
N Boulle
M Busson
M Lacroix
B S Katzenellenbogen
V Cavaillès
G Lazennec
Inserm · FRHôpital Arnaud de Villeneuve · FRUniversity of Illinois Urbana-Champaign · US

Funding

ANTIESTROGENS: MECHANISM OF ANTAGONIST ACTIONR01CA018119 · NCI · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI KATZENELLENBOGEN, BENITA S · 1985 to 2008
$2.8M
ANTIESTROGENS: MECHANISM OF ANTAGONIST ACTIONR37CA018119 · NCI · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI KATZENELLENBOGEN, BENITA S · 1991 to 1998
–
NCI NIH HHS CA18119NCI NIH HHS R01 CA018119
6 · The paper itself

Abstract

The proliferative action of ERalpha largely accounts for the carcinogenic activity of estrogens. By contrast, recent data show that ERbeta displays tumor-suppressor properties, thus supporting the interest to identify compounds that could increase its activity. Here, we show that histone deacetylase inhibitors (HDI) upregulated ERbeta protein levels, whereas it decreased ERalpha expression. Part of this regulation took place at the mRNA level through a mechanism independent of de novo protein synthesis. In addition, we found that, in various cancer cells, the treatment with different HDI enhanced the ligand-dependent activity of ERbeta more strongly than that of ERalpha. On the other hand, in MDA-MB231 and HeLa cells, the expression of ERs modified the transcriptional response to HDI. The use of deletion mutants of both receptors demonstrated that AF1 domain of the receptors was required. Finally, we show that ERbeta expression led to a dramatic increased in the antiproliferative activity of HDI, which correlated with a modification of the transcription of genes involved in cell cycle control by HDI. Altogether, these data demonstrate that the interference of ERbeta and HDAC on the control of transcription and cell proliferation constitute a promising approach for cancer therapy.

Indexed as

ApoptosisBlotting, WesternCell ProliferationEnzyme InhibitorsEstrogen Receptor alphaEstrogen Receptor betaHeLa CellsHistone DeacetylasesHumansPolymerase Chain ReactionRNA, MessengerTranscription, GeneticEnzyme InhibitorsEstrogen Receptor alphaEstrogen Receptor betaHistone DeacetylasesRNA, Messenger

Identifiers

PMID16158045
PMCPMC2034758
OpenAlexW1590835357

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.