Evidence map›Paper›PMID 33131024›Full record

ReviewJournal of mammary gland biology and neoplasia2020

Characterization of Organoid Cultures to Study the Effects of Pregnancy Hormones on the Epigenome and Transcriptional Output of Mammary Epithelial Cells.

Michael F Ciccone, Marygrace C Trousdell, Camila O Dos Santos

Open access · hybridAbstract readReview
In one paragraph

Review in Journal of mammary gland biology and neoplasia, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.9field-weighted citation impact, top 22% 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

11 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Unraveling the Breast: Advances in Mammary Biology and Cancer Methods.Journal of mammary gland biology and neoplasia · 2020
    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

3 authors at 1 institution in 1 country.

Michael F Ciccone *Cold Spring Harbor Laboratory, Cold Spring Harbor, NY, 11724, USA.
Marygrace C Trousdell *Cold Spring Harbor Laboratory, Cold Spring Harbor, NY, 11724, USA.
Camila O Dos SantosCold Spring Harbor Laboratory, Cold Spring Harbor, NY, 11724, USA. dossanto@cshl.edu.ORCID http://orcid.org/0000-0002-3999-9523
Cold Spring Harbor Laboratory · US

Funding

Single-Cell Biology Shared ResourceP30CA045508 · NCI · COLD SPRING HARBOR LABORATORY · PI David A Tuveson · 1987 to 2026
$118.9M
Probing the role of epigenomics in Brca1-deficient mammary tumors.R01CA248158 · NCI · COLD SPRING HARBOR LABORATORY · PI DOS SANTOS, CAMILA · 2020 to 2024
$2.2M
NCI NIH HHS 5P30CA045508NCI NIH HHS P30 CA045508NCI NIH HHS R01 CA248158NCI NIH HHS R01CA248158-01
6 · The paper itself

Abstract

The use of mouse derived mammary organoids can provide a unique strategy to study mammary gland development across a normal life cycle, as well as offering insights into how malignancies form and progress. Substantial cellular and epigenomic changes are triggered in response to pregnancy hormones, a reaction that engages molecular and cellular changes that transform the mammary epithelial cells into "milk producing machines". Such epigenomic alterations remain stable in post-involution mammary epithelial cells and control the reactivation of gene transcription in response to re-exposure to pregnancy hormones. Thus, a system that tightly controls exposure to pregnancy hormones, epigenomic alterations, and activation of transcription will allow for a better understanding of such molecular switches. Here, we describe the characterization of ex vivo cultures to mimic the response of mammary organoid cultures to pregnancy hormones and to understand gene regulation and epigenomic reprogramming on consecutive hormone exposure. Our findings suggest that this system yields similar epigenetic modifications to those reported in vivo, thus representing a suitable model to closely track epigenomic rearrangement and define unknown players of pregnancy-induced development.

Indexed as

AnimalsCell Culture TechniquesCell DifferentiationEnhancer of Zeste Homolog 2 ProteinEpigenesis, GeneticEpithelial CellsEstradiolFemaleHistone CodeHistonesLactationMammary Glands, AnimalMiceModels, AnimalOrganoidsPregnancyEnhancer of Zeste Homolog 2 ProteinEstradiolEzh2 protein, mouseHistonesProgesteroneProlactinEpigenomicsMammary organoidsPregnancy-induced development

Identifiers

PMID33131024
PMCPMC7960614
OpenAlexW3096362025

What Socratic 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 Socratic graph.