Evidence map›Paper›PMID 27613106›Full record

ArticleToxicologic pathology2016

Mammary Gland Evaluation in Juvenile Toxicity Studies: Temporal Developmental Patterns in the Male and Female Harlan Sprague-Dawley Rat.

Adam J Filgo, Julie F Foley, Samantha Puvanesarajah, Aditi R Borde, Bentley R Midkiff, Casey E Reed, Vesna A Chappell, Lydia B Alexander, Pretish R Borde, Melissa A Troester and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Toxicologic pathology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.6field-weighted citation impact, top 12% 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

9 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
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  3. Review
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  9. Sectioning Mammary Gland Whole Mounts for Lesion Identification.Journal of visualized experiments : JoVE · 2017
    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

12 authors at 5 institutions in 1 country.

Adam J FilgoCurriculum in Toxicology, School of Medicine, University of North Carolina, Chapel Hill, North Carolina, USA National Toxicology Program (NTP) Laboratory, Division of the NTP, National Institute of Environmental Health Sciences (NIEHS), National Institute of Health (NIH), Research Triangle Park, North Carolina, USA.
Julie F FoleyCellular and Molecular Pathology Branch, Division of the NTP, NIEHS, NIH, Research Triangle Park, North Carolina, USA.
Samantha PuvanesarajahUNC Lineberger Comprehensive Cancer Center, Chapel Hill, North Carolina, USA.
Aditi R BordeNational Toxicology Program (NTP) Laboratory, Division of the NTP, National Institute of Environmental Health Sciences (NIEHS), National Institute of Health (NIH), Research Triangle Park, North Carolina, USA.
Bentley R MidkiffDepartment of Pathology and Laboratory Medicine, University of North Carolina, Chapel Hill, North Carolina, USA.
Casey E ReedNational Toxicology Program (NTP) Laboratory, Division of the NTP, National Institute of Environmental Health Sciences (NIEHS), National Institute of Health (NIH), Research Triangle Park, North Carolina, USA.
Vesna A ChappellNational Toxicology Program (NTP) Laboratory, Division of the NTP, National Institute of Environmental Health Sciences (NIEHS), National Institute of Health (NIH), Research Triangle Park, North Carolina, USA.
Lydia B AlexanderNational Toxicology Program (NTP) Laboratory, Division of the NTP, National Institute of Environmental Health Sciences (NIEHS), National Institute of Health (NIH), Research Triangle Park, North Carolina, USA.
Pretish R BordeNational Toxicology Program (NTP) Laboratory, Division of the NTP, National Institute of Environmental Health Sciences (NIEHS), National Institute of Health (NIH), Research Triangle Park, North Carolina, USA.
Melissa A TroesterUNC Lineberger Comprehensive Cancer Center, Chapel Hill, North Carolina, USA Department of Epidemiology, University of North Carolina, Chapel Hill, North Carolina, USA.
Schantel A Hayes BouknightPathology Associates, Inc., Charles River Laboratories, Durham, North Carolina, USA.
Suzanne E FentonNational Toxicology Program (NTP) Laboratory, Division of the NTP, National Institute of Environmental Health Sciences (NIEHS), National Institute of Health (NIH), Research Triangle Park, North Carolina, USA fentonse@niehs.nih.gov.
National Institute of Environmental Health Sciences · USUNC Lineberger Comprehensive Cancer CenterCharles River Associates · USResearch Triangle Park Foundation · USUniversity of North Carolina at Chapel Hill · US

Funding

Mammary Gland as a Sensitive End Point to Effects of Endocrine DisruptorsZIAES102785 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI FENTON, SUZANNE · 2010 to 2021
$38.1M
UNC-CH CENTER FOR ENVIRONMENTAL HEALTH &SUSCEPTIBILITYP30ES010126 · NIEHS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Melissa A. Troester · 2001 to 2026
$36.3M
TOXICOLOGYT32ES007126 · NIEHS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ILONA JASPERS, Bernard E. Weissman · 1985 to 2026
$13.0M
Biology of Race and Progression Associated Breast Tumor Gene ExpressionU01CA179715 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI PEROU, CHARLES M, TROESTER, MELISSA A. · 2014 to 2018
$1.6M
Intramural NIH HHS ZIA ES102785NCI NIH HHS U01 CA179715NIEHS NIH HHS P30 ES010126NIEHS NIH HHS T32 ES007126
6 · The paper itself

Abstract

There are currently no reports describing mammary gland development in the Harlan Sprague-Dawley (HSD) rat, the current strain of choice for National Toxicology Program (NTP) testing. Our goals were to empower the NTP, contract labs, and other researchers in understanding and interpreting chemical effects in this rat strain. To delineate similarities/differences between the female and male mammary gland, data were compiled starting on embryonic day 15.5 through postnatal day 70. Mammary gland whole mounts, histology sections, and immunohistochemically stained tissues for estrogen, progesterone, and androgen receptors were evaluated in both sexes; qualitative and quantitative differences are highlighted using a comprehensive visual timeline. Research on endocrine disrupting chemicals in animal models has highlighted chemically induced mammary gland anomalies that may potentially impact human health. In order to investigate these effects within the HSD strain, 2,3,7,8-tetrachlorodibenzo-p-dioxin, diethylstilbestrol, or vehicle control was gavage dosed on gestation day 15 and 18 to demonstrate delayed, accelerated, and control mammary gland growth in offspring, respectively. We provide illustrations of normal and chemically altered mammary gland development in HSD male and female rats to help inform researchers unfamiliar with the tissue and may facilitate enhanced evaluation of both male and female mammary glands in juvenile toxicity studies.

Indexed as

AgingAnimalsDiethylstilbestrolFemaleMaleMammary Glands, AnimalPolychlorinated DibenzodioxinsPregnancyPrenatal Exposure Delayed EffectsRatsRats, Sprague-DawleyToxicity TestsDiethylstilbestrolPolychlorinated Dibenzodioxinsatlasdevelopmental exposurehistologyHSDmammary glandratsteroid receptorwhole mount

Identifiers

PMID27613106
PMCPMC5068132
OpenAlexW2508253919

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.