Evidence map›Paper›PMID 15598610›Full record

ArticleEnvironmental health perspectives2004

Phenotypic anchoring of gene expression changes during estrogen-induced uterine growth.

Jonathan G Moggs, Helen Tinwell, Tracey Spurway, Hur-Song Chang, Ian Pate, Fei Ling Lim, David J Moore, Anthony Soames, Ruth Stuckey, Richard Currie and 4 more

Open access · diamondAbstract read
In one paragraph

Article in Environmental health perspectives, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
7.2field-weighted citation impact, top 2% 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

36 citing papers in PubMed, 1 synthesis or guideline pooled it, 113 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
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  5. Article
  6. Article
  7. CCR3 antagonist impairs estradiol-induced eosinophil migration to the uterus in ovariectomized mice.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2020
    Article
  8. Article
  9. Estrogens regulate life and death in mitochondria.Journal of bioenergetics and biomembranes · 2017
    Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
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  19. Research resource: The estrogen receptor α cistrome defined by DamIP.Molecular endocrinology (Baltimore, Md.) · 2012
    Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 2 institutions in 2 countries.

Jonathan G MoggsSyngenta Central Toxicology Laboratory, Alderley Park, Cheshire SK10 4TJ, UK.
Helen Tinwell
Tracey Spurway
Hur-Song Chang
Ian Pate
Fei Ling Lim
David J Moore
Anthony Soames
Ruth Stuckey
Richard Currie
Tong Zhu
Ian Kimber
John Ashby
George Orphanides
Syngenta (United Kingdom) · GBSyngenta (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A major challenge in the emerging field of toxicogenomics is to define the relationships between chemically induced changes in gene expression and alterations in conventional toxicologic parameters such as clinical chemistry and histopathology. We have explored these relationships in detail using the rodent uterotrophic assay as a model system. Gene expression levels, uterine weights, and histologic parameters were analyzed 1, 2, 4, 8, 24, 48, and 72 hr after exposure to the reference physiologic estrogen 17 beta-estradiol (E2). A multistep analysis method, involving unsupervised hierarchical clustering followed by supervised gene ontology-driven clustering, was used to define the transcriptional program associated with E2-induced uterine growth and to identify groups of genes that may drive specific histologic changes in the uterus. This revealed that uterine growth and maturation are preceded and accompanied by a complex, multistage molecular program. The program begins with the induction of genes involved in transcriptional regulation and signal transduction and is followed, sequentially, by the regulation of genes involved in protein biosynthesis, cell proliferation, and epithelial cell differentiation. Furthermore, we have identified genes with common molecular functions that may drive fluid uptake, coordinated cell division, and remodeling of luminal epithelial cells. These data define the mechanism by which an estrogen induces organ growth and tissue maturation, and demonstrate that comparison of temporal changes in gene expression and conventional toxicology end points can facilitate the phenotypic anchoring of toxicogenomic data.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsDNA PrimersEstradiolFemaleInjections, SubcutaneousMiceMice, Inbred StrainsOrgan SizePhenotypeReverse Transcriptase Polymerase Chain ReactionRNA, MessengerUterusDNA PrimersEstradiolRNA, Messenger

Identifiers

PMID15598610
PMCPMC1247656
OpenAlexW2052701545

What OpenQuestion holds

Textmetadata
LicenceCC0
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.