Evidence map›Paper›PMID 28102330›Full record

ArticleScientific reports2017

New insights into fetal mammary gland morphogenesis: differential effects of natural and environmental estrogens.

Lucia Speroni, Maria Voutilainen, Marja L Mikkola, Skylar A Klager, Cheryl M Schaeberle, Carlos Sonnenschein, Ana M Soto

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.8field-weighted citation impact, top 11% 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

18 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
  2. Review
  3. Breast Cancer Exposomics.Life (Basel, Switzerland) · 2024
    Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Embryonic Programs in Cancer and Metastasis-Insights From the Mammary Gland.Frontiers in cell and developmental biology · 2022
    Review
  9. Review
  10. From Wingspread to CLARITY: a personal trajectory.Nature reviews. Endocrinology · 2021
    Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. 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

7 authors at 2 institutions in 2 countries.

Lucia SperoniDept. of Integrated Physiology and Pathobiology, 136 Harrison Avenue, Tufts University School of Medicine, Boston MA 02111 USA.
Maria VoutilainenDevelopmental Biology Program, Institute of Biotechnology, University of Helsinki, Finland.
Marja L MikkolaDevelopmental Biology Program, Institute of Biotechnology, University of Helsinki, Finland.
Skylar A KlagerDept. of Integrated Physiology and Pathobiology, 136 Harrison Avenue, Tufts University School of Medicine, Boston MA 02111 USA.
Cheryl M SchaeberleDept. of Integrated Physiology and Pathobiology, 136 Harrison Avenue, Tufts University School of Medicine, Boston MA 02111 USA.
Carlos SonnenscheinDept. of Integrated Physiology and Pathobiology, 136 Harrison Avenue, Tufts University School of Medicine, Boston MA 02111 USA.
Ana M SotoDept. of Integrated Physiology and Pathobiology, 136 Harrison Avenue, Tufts University School of Medicine, Boston MA 02111 USA.
Tufts University · USUniversity of Helsinki · FI

Funding

Mechanisms of developmental toxicity of Bisphenol-AR01ES008314 · NIEHS · TUFTS UNIVERSITY BOSTON · PI SOTO, ANA · 1996 to 2016
$6.8M
NIEHS NIH HHS R01 ES008314
6 · The paper itself

Abstract

An increased breast cancer risk during adulthood has been linked to estrogen exposure during fetal life. However, the impossibility of removing estrogens from the feto-maternal unit has hindered the testing of estrogen's direct effect on mammary gland organogenesis. To overcome this limitation, we developed an ex vivo culture method of the mammary gland where the direct action of estrogens can be tested during embryonic days (E)14 to 19. Mouse mammary buds dissected at E14 and cultured for 5 days showed that estrogens directly altered fetal mammary gland development. Exposure to 0.1 pM, 10 pM, and 1 nM 17 β-estradiol (E2) resulted in monotonic inhibition of mammary buds ductal growth. In contrast, Bisphenol-A (BPA) elicited a non-monotonic response. At environmentally relevant doses (1 nM), BPA significantly increased ductal growth, as previously observed in vivo, while 1 μM BPA significantly inhibited ductal growth. Ductal branching followed the same pattern. This effect of BPA was blocked by Fulvestrant, a full estrogen antagonist, while the effect of estradiol was not. This method may be used to study the hormonal regulation of mammary gland development, and to test newly synthesized chemicals that are released into the environment without proper assessment of their hormonal action on critical targets like the mammary gland.

Indexed as

AnimalsBenzhydryl CompoundsBisphenol A CompoundsCell ProliferationEstradiolFemaleFetusFulvestrantMammary Glands, AnimalMiceMorphogenesisPhenolsPregnancyReceptors, EstrogenReceptors, G-Protein-CoupledBenzhydryl Compoundsbisphenol ABisphenol A CompoundsEstradiolFulvestrantGPER1 protein, mousePhenolsReceptors, EstrogenReceptors, G-Protein-Coupled

Identifiers

PMID28102330
PMCPMC5244390
OpenAlexW2574339288

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.