Evidence map›Paper›PMID 24190884›Full record

ArticleJournal of cell science2014

Paracrine-rescued lobulogenesis in chimeric outgrowths comprising progesterone-receptor-null mammary epithelium and redirected wild-type testicular cells.

Robert D Bruno, Corinne A Boulanger, Sonia M Rosenfield, Lisa H Anderson, John P Lydon, Gilbert H Smith

Open access · bronzeAbstract read
In one paragraph

Article in Journal of cell science, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.2field-weighted citation impact, top 35% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
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  3. Article
  4. Article
  5. Journal of cell science · 2017
    Article
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  7. Review
  8. Review
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

6 authors at 2 institutions in 1 country.

Robert D BrunoMammary Stem Cell Biology Section, CCBB, CCR, NCI, Bethesda, MD 20892, USA.
Corinne A Boulanger
Sonia M Rosenfield
Lisa H Anderson
John P Lydon
Gilbert H Smith
Baylor College of Medicine · USOld Dominion University · US

Funding

Biology of Mammary Gland Development and TumorigenesisZIABC010021 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI SMITH, GILBERT · 2009 to 2020
$11.6M
PROGESTERONE RECEPTOR IN BREAST DEVELOPMENT AND CANCERR01CA077530 · NCI · BAYLOR COLLEGE OF MEDICINE · PI LYDON, JOHN P · 2005 to 2008
$1.2M
PROGESTERONE RECEPTOR AND BREAST CANCERR29CA077530 · NCI · BAYLOR COLLEGE OF MEDICINE · PI LYDON, JOHN P · 1998 to 2004
$398k
Effectiveness and Patient Selection in Post-Hospital Brain Injury RehabilitationR03HD077495 · NICHD · INDIANA UNIVERSITY INDIANAPOLIS · PI MALEC, JAMES F. · 2014 to 2015
$154k
NCI NIH HHS CA-77530NCI NIH HHS R01 CA077530NCI NIH HHS R29 CA077530NICHD NIH HHS R03 HD077495NICHD NIH HHS U54 HD-0077495
6 · The paper itself

Abstract

We have previously shown that non-mammary and tumorigenic cells can respond to the signals of the mammary niche and alter their cell fate to that of mammary epithelial progenitor cells. Here we tested the hypothesis that paracrine signals from mammary epithelial cells expressing progesterone receptor (PR) are dispensable for redirection of testicular cells, and that re-directed wild-type testicular-derived mammary cells can rescue lobulogenesis of PR-null mammary epithelium by paracrine signaling during pregnancy. We injected PR-null epithelial cells mixed with testicular cells from wild-type adult male mice into cleared fat-pads of recipient mice. The testicular cells were redirected in vivo to mammary epithelial cell fate during regeneration of the mammary epithelium, and persisted in second-generation outgrowths. In the process, the redirected testicular cells rescued the developmentally deficient PR-null cells, signaling them through the paracrine factor RANKL to produce alveolar secretory structures during pregnancy. This is the first demonstration that paracrine signaling required for alveolar development is not required for cellular reprogramming in the mammary gland, and that reprogrammed testicular cells can provide paracrine signals to the surrounding mammary epithelium.

Indexed as

Adipose TissueAnimalsCell DifferentiationCellular ReprogrammingEpithelial CellsFemaleGene ExpressionInjectionsMaleMammary Glands, AnimalMiceParacrine CommunicationPregnancyProgesteroneRANK LigandReceptors, ProgesteroneProgesteroneRANK LigandReceptors, ProgesteroneTnfsf11 protein, mouseCellular reprogrammingMammaryProgesterone receptorRANKL

Identifiers

PMID24190884
PMCPMC3874781
OpenAlexW2131622950

What OpenQuestion holds

Textmetadata
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.