Evidence map›Paper›PMID 24465770›Full record

ArticlePloS one2014

Bisphenol A exposure alters developmental gene expression in the fetal rhesus macaque uterus.

Kathryn C Calhoun, Elizabeth Padilla-Banks, Wendy N Jefferson, Liwen Liu, Kevin E Gerrish, Steven L Young, Charles E Wood, Patricia A Hunt, Catherine A Vandevoort, Carmen J Williams

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
7.0field-weighted citation impact, top 3% 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

27 citing papers in PubMed, 56 citations in OpenAlex.

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  8. Prenatal Bisphenol A Exposure Alters Epithelial Cell Composition in the Rhesus Macaque Fetal Oviduct.Toxicological sciences : an official journal of the Society of Toxicology · 2019
    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

10 authors at 5 institutions in 1 country.

Kathryn C CalhounReproductive Medicine Group, Laboratory of Reproductive & Developmental Toxicology, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina, United States of America ; Department of Obstetrics and Gynecology, Division of Reproductive Endocrinology and Infertility, University of North Carolina-Chapel Hill, Chapel Hill, North Carolina, United States of America.
Elizabeth Padilla-BanksReproductive Medicine Group, Laboratory of Reproductive & Developmental Toxicology, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina, United States of America.
Wendy N JeffersonReproductive Medicine Group, Laboratory of Reproductive & Developmental Toxicology, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina, United States of America.
Liwen LiuMicroarray Group, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina, United States of America.
Kevin E GerrishMicroarray Group, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina, United States of America.
Steven L YoungDepartment of Obstetrics and Gynecology, Division of Reproductive Endocrinology and Infertility, University of North Carolina-Chapel Hill, Chapel Hill, North Carolina, United States of America.
Charles E WoodNational Health and Environmental Effects Research Laboratory, Office of Research and Development, US Environmental Protection Agency, Research Triangle Park, North Carolina, United States of America.
Patricia A HuntSchool of Molecular Biosciences, Washington State University, Pullman, Washington, United States of America.
Catherine A VandevoortDepartment of Obstetrics and Gynecology and California National Primate Research Center, University of California Davis, Davis, California, United States of America.
Carmen J WilliamsReproductive Medicine Group, Laboratory of Reproductive & Developmental Toxicology, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina, United States of America.
National Institute of Environmental Health Sciences · USUniversity of North Carolina at Chapel Hill · USResearch Triangle Park Foundation · USUniversity of California, Davis · USWashington State University · US

Funding

National Institute on Aging (NIA) ColonyP51OD011107 · OD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Simon J. Atkinson · 2012 to 2026
$191.5M
ZONA PELLUCIDA PEPTIDES AS IMMUNOCONTRACEPTIVE ANTIGENSP51RR000169 · NCRR · UNIVERSITY OF CALIFORNIA DAVIS · PI HYDE, DALLAS MELVIN · 1985 to 2011
$126.2M
Gene Expression and MicroarraysZICES102445 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI GERRISH, KEVIN · 2009 to 2025
$31.6M
Environmental influence on reproductive tract functionZIAES102405 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI WILLIAMS, CARMEN · 2009 to 2025
$20.6M
Meiotic Studies of Chemicals With Estrogenic ActivityR01ES013527 · NIEHS · WASHINGTON STATE UNIVERSITY · PI HUNT, PATRICIA · 2005 to 2014
$4.5M
Progesterone Action in the Endometrium of Women with EndometriosisR01HD067721 · NICHD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI YOUNG, STEVEN L · 2011 to 2015
$3.1M
Effects of Fetal Bisphenol A Exposure on Oogenesis in PrimatesR01ES016770 · NIEHS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI HUNT, PATRICIA, VANDEVOORT, CATHERINE A · 2008 to 2010
$1.8M
Meiotic Studies of Chemicals with Estrogenic ActivityR56ES013527 · NIEHS · WASHINGTON STATE UNIVERSITY · PI GERONA, ROY ROBERTO R, HUNT, PATRICIA · 2017 to 2017
$250k
Intramural NIH HHSNCRR NIH HHS P51 RR000169NIEHS NIH HHS ES013527NIEHS NIH HHS ES016770NIEHS NIH HHS ES102405NIEHS NIH HHS R01 ES013527NIEHS NIH HHS R01 ES016770NIEHS NIH HHS R56 ES013527NIH HHS P51 OD011107
6 · The paper itself

Abstract

Bisphenol A (BPA) exposure results in numerous developmental and functional abnormalities in reproductive organs in rodent models, but limited data are available regarding BPA effects in the primate uterus. To determine if maternal oral BPA exposure affects fetal uterine development in a non-human primate model, pregnant rhesus macaques carrying female fetuses were exposed orally to 400 µg/kg BPA or vehicle control daily from gestation day (GD) 50-100 or GD100-165. Fetal uteri were collected at the completion of treatment (GD100 or GD165); tissue histology, cell proliferation, and expression of estrogen receptor alpha (ERα) and progesterone receptor (PR) were compared to that of controls. Gene expression analysis was conducted using rhesus macaque microarrays. There were no significant differences in histology or in the percentage of cells expressing the proliferation marker Ki-67, ERα, or PR in BPA-exposed uteri compared to controls at GD100 or GD165. Minimal differences in gene expression were observed between BPA-exposed and control GD100 uteri. However, at GD165, BPA-exposed uteri had significant differences in gene expression compared to controls. Several of the altered genes, including HOXA13, WNT4, and WNT5A, are critical for reproductive organ development and/or adult function. We conclude that second or third trimester BPA exposure does not significantly affect fetal uterus development based on morphological, proliferation, and steroid hormone receptor assessments. However, differences in expression of key developmental genes after third trimester exposure suggest that BPA could alter transcriptional signals influencing uterine function later in life.

Indexed as

AnimalsBenzhydryl Compoundsbeta CateninBisphenol A CompoundsEndocrine DisruptorsEnvironmental ExposureEstrogen Receptor alphaFemaleFetal DevelopmentGene Expression Regulation, DevelopmentalGene Regulatory NetworksMacaca mulattaMaternal ExposureMaternal-Fetal ExchangeOligonucleotide Array Sequence AnalysisPhenolsBenzhydryl Compoundsbeta Cateninbisphenol ABisphenol A CompoundsEndocrine DisruptorsEstrogen Receptor alphaPhenolsReceptors, Progesterone

Identifiers

PMID24465770
PMCPMC3900442
OpenAlexW2038472343

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.