Evidence map›Paper›PMID 20870566›Full record

ArticleEnvironmental health perspectives2011

Combinations of physiologic estrogens with xenoestrogens alter ERK phosphorylation profiles in rat pituitary cells.

Yow-Jiun Jeng, Cheryl S Watson

Open access · diamondAbstract read
In one paragraph

Article in Environmental health perspectives, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

24 citing papers in PubMed, 60 citations in OpenAlex.

  1. Estrogenic activity in tampon products.Journal of the Endocrine Society · 2026
    Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Role of ER-α36 in breast cancer by typical xenoestrogens.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2015
    Review
  11. Effects of oral exposure to bisphenol A on gene expression and global genomic DNA methylation in the prostate, female mammary gland, and uterus of NCTR Sprague-Dawley rats.Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association · 2015
    Article
  12. Review
  13. Neurological Effects of Bisphenol A and its Analogues.International journal of medical sciences · 2015
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Designing Endocrine Disruption Out of the Next Generation of Chemicals.Green chemistry : an international journal and green chemistry resource : GC · 2013
    Article
  19. Non-genomic effects of xenoestrogen mixtures.International journal of environmental research and public health · 2012
    Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Yow-Jiun JengDepartment of Biochemistry and Molecular Biology, University of Texas Medical Branch, Galveston, Texas 77555-0645, USA.
Cheryl S Watson
The University of Texas Medical Branch at Galveston · US

Funding

Nongenomic Signaling Mechanisms of Environmental EstrogensR01ES015292 · NIEHS · UNIVERSITY OF TEXAS MED BR GALVESTON · PI WATSON, CHERYL S · 2007 to 2011
$1.2M
NIEHS NIH HHS R01 ES015292
6 · The paper itself

Abstract

backgroundEstrogens are potent nongenomic phospho-activators of extracellular-signal-regulated kinases (ERKs). A major concern about the toxicity of xenoestrogens (XEs) is potential alteration of responses to physiologic estrogens when XEs are present simultaneously.

objectivesWe examined estrogen-induced ERK activation, comparing the abilities of structurally related XEs (alkylphenols and bisphenol A) to alter ERK responses induced by physiologic concentrations (1 nM) of estradiol (E2), estrone (E1), and estriol (E3).

methodsWe quantified hormone/mimetic-induced ERK phosphorylations in the GH3/B6/F10 rat pituitary cell line using a plate immunoassay, comparing effects with those on cell proliferation and by estrogen receptor subtype-selective ligands.

resultsAlone, these structurally related XEs activate ERKs in an oscillating temporal pattern similar (but not identical) to that with physiologic estrogens. The potency of all estrogens was similar (active between femtomolar and nanomolar concentrations). XEs potently disrupted physiologic estrogen signaling at low, environmentally relevant concentrations. Generally, XEs potentiated (at the lowest, subpicomolar concentrations) and attenuated (at the highest, picomolar to 100 nM concentrations) the actions of the physiologic estrogens. Some XEs showed pronounced nonmonotonic responses/inhibitions. The phosphorylated ERK and proliferative responses to receptor-selective ligands were only partially correlated.

conclusionsXEs are both imperfect potent estrogens and endocrine disruptors; the more efficacious an XE, the more it disrupts actions of physiologic estrogens. This ability to disrupt physiologic estrogen signaling suggests that XEs may disturb normal functioning at life stages where actions of particular estrogens are important (e.g., development, reproductive cycling, pregnancy, menopause).

Indexed as

AnimalsCell Line, TumorCell ProliferationEndocrine DisruptorsEnvironmental PollutantsEstrogensExtracellular Signal-Regulated MAP KinasesPhenolsPhosphorylationPituitary GlandRatsReceptors, EstrogenSignal TransductionEndocrine DisruptorsEnvironmental PollutantsEstrogensExtracellular Signal-Regulated MAP KinasesPhenolsReceptors, Estrogen

Identifiers

PMID20870566
PMCPMC3018487
OpenAlexW2040965131

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Read underepoch 390

Registered trials

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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.