Evidence map›Paper›PMID 25405629›Full record

ArticlePloS one2014

Differential roles of ERα and ERβ in normal and neoplastic development in the mouse mammary gland.

Rajendra G Mehta, Michael Hawthorne, Rajeshwari R Mehta, Karen E O Torres, Xinjian Peng, David L McCormick, Levy Kopelovich

Open access · goldAbstract readComparative Study
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 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

12 citing papers in PubMed, 23 citations in OpenAlex.

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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

7 authors at 2 institutions in 1 country.

Rajendra G MehtaIIT Research Institute, Chicago, Illinois, United States of America.
Michael HawthorneIIT Research Institute, Chicago, Illinois, United States of America.
Rajeshwari R MehtaIIT Research Institute, Chicago, Illinois, United States of America.
Karen E O TorresGenUs Biosystems, Northbrook, Illinois, United States of America.
Xinjian PengIIT Research Institute, Chicago, Illinois, United States of America.
David L McCormickIIT Research Institute, Chicago, Illinois, United States of America.
Levy KopelovichDivision of Cancer Prevention, National Cancer Institute, Rockville, Maryland, United States of America.
IIT Research Institute · USNational Cancer Institute · US

Funding

NCI NIH HHS N01 CN043301
6 · The paper itself

Abstract

The present experiments were performed to determine the roles of estrogen receptors α and β (ERα and ERβ) in normal and neoplastic development in the mouse mammary gland. In wild-type mice, in vivo administration of estradiol (E) + progesterone (P) stimulated mammary ductal growth and alveolar differentiation. Mammary glands from mice in which the ERβ gene has been deleted (βERKO mice) demonstrated normal ductal growth and differentiation in response to E + P. By contrast, mammary glands from mice in which the ERα gene has been deleted (αERKO mice) demonstrated only rudimentary ductal structures that did not differentiate in response to E + P. EGF demonstrates estrogen-like activity in the mammary glands of αERKO mice: treatment of αERKO mice with EGF + P (without E) supported normal mammary gland development, induced expression of progesterone receptor (PR), and increased levels of G-protein-coupled receptor (GPR30) protein. Mammary gland development in βERKO mice treated with EGF + P was comparable to that of wild-type mice receiving EGF + P; EGF had no statistically significant effects on the induction of PR or expression of GPR30 in mammary glands harvested from either wild-type mice or βERKO mice. In vitro exposure of mammary glands to 7,12-dimethylbenz[a]anthracene (DMBA) induced preneoplastic mammary alveolar lesions (MAL) in glands from wild-type mice and βERKO mice, but failed to induce MAL in mammary glands from αERKO mice. Microarray analysis of DMBA-treated mammary glands identified 28 functional pathways whose expression was significantly different in αERKO mice versus both βERKO and wild-type mice; key functions that were differentially expressed in αERKO mice included cell division, cell proliferation, and apoptosis. The data demonstrate distinct roles for ERα and ERβ in normal and neoplastic development in the mouse mammary gland, and suggest that EGF can mimic the ERα-mediated effects of E in this organ.

Indexed as

9,10-Dimethyl-1,2-benzanthraceneAnimalsBreast NeoplasmsDNA PrimersEstradiolEstrogen Receptor alphaEstrogen Receptor betaFemaleHumansImmunohistochemistryMammary Glands, HumanMiceMice, KnockoutMicroarray AnalysisProgesteroneReal-Time Polymerase Chain Reaction9,10-Dimethyl-1,2-benzanthraceneDNA PrimersEstradiolEstrogen Receptor alphaEstrogen Receptor betaGPER1 protein, mouseProgesteroneReceptors, EstrogenReceptors, G-Protein-Coupled

Identifiers

PMID25405629
PMCPMC4236140
OpenAlexW2076542036

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.