Evidence map›Paper›PMID 11746508›Full record

ArticleJournal of cellular biochemistry2001

Trichostatin A inhibits beta-casein expression in mammary epithelial cells.

P Pujuguet, D Radisky, D Levy, C Lacza, M J Bissell

Open access · greenAbstract read
In one paragraph

Article in Journal of cellular biochemistry, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.4field-weighted citation impact, top 37% 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

14 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Effects of Trichostatin A on Cumulus Expansion during Mouse Oocyte Maturation.Asian-Australasian journal of animal sciences · 2013
    Article
  3. Growth of lung cancer cells in three-dimensional microenvironments reveals key features of tumor malignancy.Integrative biology : quantitative biosciences from nano to macro · 2012
    Article
  4. Epigenetic regulation of milk production in dairy cows.Journal of mammary gland biology and neoplasia · 2010
    Review
  5. Article
  6. Adipose-depleted mammary epithelial cells and organoids.Journal of mammary gland biology and neoplasia · 2009
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. Article
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

5 authors at 1 institution in 1 country.

P PujuguetLife Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, USA.
D Radisky
D Levy
C Lacza
M J Bissell
Lawrence Berkeley National Laboratory · US

Funding

Role of Metalloproteinases in Mammary Gland RemodelingR01CA057621 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WERB, ZENA · 1993 to 2017
$9.0M
NCI NIH HHS CA-57621-02NCI NIH HHS R01 CA057621
6 · The paper itself

Abstract

Many aspects of cellular behavior are defined by the content of information provided by association of the extracellular matrix (ECM) and with cell membrane receptors. When cultured in the presence of laminin-containing ECM and prolactin (Prl), normal mammary epithelial cells express the milk protein beta-casein. We have previously found that the minimal ECM- and Prl-responsive enhancer element BCE-1 was only active when stably integrated into chromatin, and that trichostatin A (TSA), a reagent that leads to alterations in chromatin structure, was able to activate the integrated enhancer element. We now show that endogenous beta-casein gene, which is controlled by a genetic assembly that is highly similar to that of BCE-1 and which is also activated by incubation in ECM and Prl, is instead inhibited by TSA. We provide evidence that the differing response of beta-casein and BCE-1 to TSA is neither due to an unusual effect of TSA on mammary epithelial cells, nor to secondary consequences from the expression of a separate gene, nor to a particular property of the BCE-1 construct. As a component of this investigation, we also showed that ECM mediated rapid histone deacetylation in mammary epithelial cells. These results are discussed in combination with previous work showing that TSA mediates the differentiation of many types of cancer cells but inhibits differentiation of some nonmalignant cell types.

Indexed as

Saccharomyces cerevisiae ProteinsAcetylationAcetyltransferasesAnimalsBasement MembraneCaseinsCattleCell LineChromatinEnhancer Elements, GeneticEpithelial CellsGenes, ReporterHistone AcetyltransferasesHistonesHydroxamic AcidsMammary Glands, AnimalAcetyltransferasesCaseinsChromatinHistone AcetyltransferasesHistonesHydroxamic AcidsMembrane ProteinsProtein Synthesis InhibitorsRecombinant ProteinsSaccharomyces cerevisiae Proteinstrichostatin A

Identifiers

PMID11746508
PMCPMC2949289
OpenAlexW1992168084

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.