Evidence map›Paper›PMID 24284790›Full record

ArticleToxicological sciences : an official journal of the Society of Toxicology2014

Coexposure to phytoestrogens and bisphenol a mimics estrogenic effects in an additive manner.

Anne Katchy, Caroline Pinto, Philip Jonsson, Trang Nguyen-Vu, Marchela Pandelova, Anne Riu, Karl-Werner Schramm, Daniel Samarov, Jan-Åke Gustafsson, Maria Bondesson and 1 more

Abstract read
In one paragraph

Article in Toxicological sciences : an official journal of the Society of Toxicology, 2014. 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
4.3field-weighted citation impact, top 6% 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, 54 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Expression Profiles of Estrogen-Regulated MicroRNAs in Cancer Cells.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  8. Article
  9. What Does CLARITY-BPA Mean for Canadians?International journal of environmental research and public health · 2021
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
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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

11 authors at 4 institutions in 3 countries.

Anne Katchy* Center for Nuclear Receptors and Cell Signaling, Department of Biology and Biochemistry, University of Houston, Houston, Texas 77204-5056;
Caroline Pinto
Philip Jonsson
Trang Nguyen-Vu
Marchela Pandelova
Anne Riu
Karl-Werner Schramm
Daniel Samarov
Jan-Åke Gustafsson
Maria Bondesson
Cecilia Williams
University of Houston · USHelmholtz Zentrum München · DEKarolinska Institutet · SENational Institute of Standards and Technology · US

Funding

Elucidating the mechanism of ERbeta in colon carcinogenesisR01CA172437 · NCI · UNIVERSITY OF HOUSTON · PI WILLIAMS, CECILIA MARIE · 2013 to 2018
$1.4M
Detection of Obesogens and Diabetogens by Zebrafish Screening ModelsR21ES020036 · NIEHS · UNIVERSITY OF HOUSTON · PI GUSTAFSSON, JAN-AKE · 2012 to 2013
$371k
NCI NIH HHS R01 CA172437NCI NIH HHS R01CA172437NIEHS NIH HHS 1R21ES020036
6 · The paper itself

Abstract

Endocrine-disrupting chemicals (EDC) are abundant in our environment. A number of EDCs, including bisphenol A (BPA) can bind to the estrogen receptors (ER), ERα and ERβ, and may contribute to estrogen-linked diseases such as breast cancer. Early exposure is of particular concern; many EDCs cross the placenta and infants have measurable levels of, eg, BPA. In addition, infants are frequently fed soy-based formula (SF) that contains phytoestrogens. Effects of combined exposure to xeno- and phytoestrogens are poorly studied. Here, we extensively compared to what extent BPA, genistein, and an extract of infant SF mimic estrogen-induced gene transcription and cell proliferation. We investigated ligand-specific effects on ER activation in HeLa-ERα and ERβ reporter cells; on proliferation, genome-wide gene regulation and non-ER-mediated effects in MCF7 breast cancer cells; and how coexposure influenced these effects. The biological relevance was explored using enrichment analyses of differentially regulated genes and clustering with clinical breast cancer profiles. We demonstrate that coexposure to BPA and genistein, or SF, results in increased functional and transcriptional estrogenic effects. Using statistical modeling, we determine that BPA and phytoestrogens act in an additive manner. The proliferative and transcriptional effects of the tested compounds mimic those of 17β-estradiol, and are abolished by cotreatment with an ER antagonist. Gene expression profiles induced by each compound clustered with poor prognosis breast cancer, indicating that exposure may adversely affect breast cancer prognosis. This study accentuates that coexposure to BPA and soy-based phytoestrogens results in additive estrogenic effects, and may contribute to estrogen-linked diseases, including breast cancer.

Indexed as

Benzhydryl CompoundsBisphenol A CompoundsCell ProliferationDose-Response Relationship, DrugDrug SynergismEndocrine DisruptorsEstrogen Receptor alphaEstrogen Receptor betaGenes, ReporterGenisteinHeLa CellsHumansInfantInfant FormulaIsoflavonesMCF-7 CellsBenzhydryl Compoundsbisphenol ABisphenol A CompoundsdaidzinEndocrine DisruptorsESR1 protein, humanEstrogen Receptor alphaEstrogen Receptor betaGenisteinIsoflavonesPhenolsPhytoestrogensbisphenol Aconcentration addition.estrogen receptorphytoestrogensproliferationtranscriptional activation

Identifiers

PMID24284790
PMCPMC3930363
OpenAlexW2140430039

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.