Evidence map›Paper›PMID 32056248›Full record

ArticleAlcoholism, clinical and experimental research2020

Fetal Alcohol Exposure Alters Mammary Epithelial Cell Subpopulations and Promotes Tumorigenesis.

Mariana Saboya, Amanda E Jetzt, Ketaki Datar, Wendie S Cohick

Open access · greenAbstract read
In one paragraph

Article in Alcoholism, clinical and experimental research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

4 authors at 1 institution in 1 country.

Mariana SaboyaFrom the, The Department of Animal Sciences, Rutgers, The State University of New Jersey, New Brunswick, NJ.
Amanda E JetztFrom the, The Department of Animal Sciences, Rutgers, The State University of New Jersey, New Brunswick, NJ.ORCID 0000-0001-9312-0121
Ketaki DatarFrom the, The Department of Animal Sciences, Rutgers, The State University of New Jersey, New Brunswick, NJ.
Wendie S CohickFrom the, The Department of Animal Sciences, Rutgers, The State University of New Jersey, New Brunswick, NJ.ORCID 0000-0002-6747-1558
Rutgers, The State University of New Jersey · US

Funding

TRANSCRIPTIONAL PROFILINGP30CA072720 · NCI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI Chang S Chan · 1997 to 2026
$94.5M
Translational Research Support CoreP30ES005022 · NIEHS · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI ROBERT John LAUMBACH · 1988 to 2026
$47.4M
Beckman Coulter MoFlo Astrios EQ Cell SorterS10OD026876 · OD · RUTGERS, THE STATE UNIV OF N.J. · PI LASKIN, DEBRA L · 2019 to 2019
$504k
Fluorescence Activated Cell SorterS10RR025468 · NCRR · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI LATTIME, EDMUND C. · 2009 to 2009
$500k
NCI NIH HHS P30 CA072720NCRR NIH HHS S10 RR025468NIEHS NIH HHS P30 ES005022NIH HHS S10 OD026876
6 · The paper itself

Abstract

backgroundFetal alcohol exposure (FAE) increases the risk of mammary tumorigenesis in adult offspring; however, the underlying mechanism remains unknown. This study tested the hypothesis that FAE shifts the mammary epithelial cell (MEC) composition toward one that promotes tumorigenesis.

methodsPregnant Friend Virus B NIH Jackson dams bred to MMTV-Wnt1 male mice were given ad libitum access to 5% alcohol in 0.2% saccharin solution from GD9-10 and 10% alcohol in 0.2% saccharin from GD11-GD19 or 0.2% saccharin solution from GD9-GD19. Thoracic and inguinal mammary glands from wild-type (WT) and transgenic (Tg) female offspring were harvested at 5 and 10 weeks of age and dissociated to yield a single cell suspension enriched for MECs for flow cytometry, mammosphere assay, and gene analysis. A subset of Tg offspring was followed for tumor formation.

resultsWT glands of FAE animals exhibited a decreased basal cell population and increased luminal: basal ratio at 10 weeks of age. qRT-PCR analysis of total MECs found that Hey1 mRNA expression was increased in the WT FAE group at 10 weeks of age. In Tg glands, FAE increased the luminal progenitor cell population at 5 weeks of age but did not alter MEC composition at 10 weeks of age. Tertiary mammosphere-forming efficiency was greater in the WT glands of FAE animals at 10 weeks of age. Tumor latency was decreased in the FAE group. Flow cytometry analysis indicated that FAE females developed tumors with an increased basal cell population.

conclusionsThese data indicate that FAE can shift MEC subpopulations, increasing the proportion of cells that are potentially vulnerable to transformation and affecting cancer risk.

Indexed as

Prenatal Exposure Delayed EffectsAnimalsCarcinogenesisCentral Nervous System DepressantsEpithelial CellsEthanolFemaleFlow CytometryMammary Glands, AnimalMammary Neoplasms, AnimalMicePregnancyTranscriptomeCentral Nervous System DepressantsEthanolAlcohol exposure in uteroBreast cancerFetal alcohol exposureMammary epithelial cell lineage

Identifiers

PMID32056248
PMCPMC7166183
OpenAlexW3006190684

What OpenQuestion holds

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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.