Evidence map›Paper›PMID 19969081›Full record

ArticleThe Journal of steroid biochemistry and molecular biology2010

Cell density is a critical determinant of aromatase expression in adipose stromal cells.

Sagar Ghosh, Yanfen Hu, Rong Li

Abstract read
In one paragraph

Article in The Journal of steroid biochemistry and molecular biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 39% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Effect of body mass index on postoperative transfusions and 24-hour chest-tube output.The International journal of angiology : official publication of the International College of Angiology, Inc · 2011
    Article
  5. 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

3 authors at 1 institution in 1 country.

Sagar GhoshDepartment of Molecular Medicine, Institute of Biotechnology, 15335 Lambda Drive, University of Texas, Health Science Center at San Antonio, San Antonio, TX 78245, USA.
Yanfen Hu
Rong Li
The University of Texas Health Science Center at San Antonio · US

Funding

BRCA1 IN GENE REGULATION AND TUMOR SUPPRESSIONR01CA093506 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI LI, RONG · 2002 to 2010
$2.3M
The Mechanism of BRCA1 in Tumor SuppressionR01CA118578 · NCI · UNIVERSITY OF VIRGINIA · PI HU, YANFEN · 2006 to 2010
$1.1M
NCI NIH HHS CA118578NCI NIH HHS CA93506NCI NIH HHS R01 CA093506NCI NIH HHS R01 CA118578
6 · The paper itself

Abstract

Obesity is associated with an increased risk of breast cancer among postmenopausal women. This is at least partly due to excessive estrogen production in adipose tissue of obese women. Aromatase, the key enzyme in estrogen biosynthesis, is an important target in endocrine therapy for estrogen receptor (ER)-positive postmenopausal breast cancer. In this study we show that high confluency of human adipose stromal cells (ASCs) cultured in vitro can significantly stimulate aromatase gene expression and reduce the expression of breast tumor suppressor BRCA1 and members of the NR4A orphan nuclear family. Furthermore, small interfering RNA (siRNA)-mediated knockdown of Nurr1, a member of the NR4A family, substantially increased aromatase expression. Lastly, we found that the cell density-triggered inducibility of aromatase expression varies in ASCs isolated from different disease-free individuals. Our finding highlights the impact of increased cell number on estrogen biosynthesis as in the case of excessive adiposity.

Indexed as

Cell CountGene Expression Regulation, EnzymologicAdipose TissueAromataseBRCA1 ProteinCell Line, TumorCells, CulturedCohort StudiesFemaleGene Expression Regulation, NeoplasticHumansNuclear Receptor Subfamily 4, Group A, Member 1Nuclear Receptor Subfamily 4, Group A, Member 2Stromal CellsAromataseBRCA1 ProteinNR4A2 protein, humanNuclear Receptor Subfamily 4, Group A, Member 1Nuclear Receptor Subfamily 4, Group A, Member 2

Identifiers

PMID19969081
PMCPMC2826521
OpenAlexW1983639420

What OpenQuestion holds

Textmetadata
LicenceTDM
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.