Evidence map›Paper›PMID 26581094›Full record

ArticlePLoS genetics2015

Ectodysplasin/NF-κB Promotes Mammary Cell Fate via Wnt/β-catenin Pathway.

Maria Voutilainen, Päivi H Lindfors, Ewelina Trela, Darielle Lönnblad, Vera Shirokova, Teresa Elo, Elisa Rysti, Ruth Schmidt-Ullrich, Pascal Schneider, Marja L Mikkola

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

14 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Embryonic Mammary Gland Morphogenesis.Advances in experimental medicine and biology · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. The Role of Ectodysplasin A on the Ocular Surface Homeostasis.International journal of molecular sciences · 2022
    Review
  9. Cell signaling regulation in salivary gland development.Cellular and molecular life sciences : CMLS · 2021
    Review
  10. Frontiers in physiology · 2020
    Article
  11. Article
  12. Article
  13. Article
  14. 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

10 authors at 3 institutions in 3 countries.

Maria VoutilainenDevelopmental Biology Program, Institute of Biotechnology, University of Helsinki, Helsinki, Finland.
Päivi H LindforsDevelopmental Biology Program, Institute of Biotechnology, University of Helsinki, Helsinki, Finland.
Ewelina TrelaDevelopmental Biology Program, Institute of Biotechnology, University of Helsinki, Helsinki, Finland.
Darielle LönnbladDevelopmental Biology Program, Institute of Biotechnology, University of Helsinki, Helsinki, Finland.
Vera ShirokovaDevelopmental Biology Program, Institute of Biotechnology, University of Helsinki, Helsinki, Finland.
Teresa EloDevelopmental Biology Program, Institute of Biotechnology, University of Helsinki, Helsinki, Finland.
Elisa RystiDevelopmental Biology Program, Institute of Biotechnology, University of Helsinki, Helsinki, Finland.
Ruth Schmidt-UllrichMax-Delbrück-Center for Molecular Medicine, Berlin, Germany.
Pascal SchneiderDepartment of Biochemistry, University of Lausanne, Epalinges, Switzerland.
Marja L MikkolaDevelopmental Biology Program, Institute of Biotechnology, University of Helsinki, Helsinki, Finland.
University of Helsinki · FIMax Delbrück Center · DEUniversity of Lausanne · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mammary gland development commences during embryogenesis with the establishment of a species typical number of mammary primordia on each flank of the embryo. It is thought that mammary cell fate can only be induced along the mammary line, a narrow region of the ventro-lateral skin running from the axilla to the groin. Ectodysplasin (Eda) is a tumor necrosis factor family ligand that regulates morphogenesis of several ectodermal appendages. We have previously shown that transgenic overexpression of Eda (K14-Eda mice) induces formation of supernumerary mammary placodes along the mammary line. Here, we investigate in more detail the role of Eda and its downstream mediator transcription factor NF-κB in mammary cell fate specification. We report that K14-Eda mice harbor accessory mammary glands also in the neck region indicating wider epidermal cell plasticity that previously appreciated. We show that even though NF-κB is not required for formation of endogenous mammary placodes, it is indispensable for the ability of Eda to induce supernumerary placodes. A genome-wide profiling of Eda-induced genes in mammary buds identified several Wnt pathway components as potential transcriptional targets of Eda. Using an ex vivo culture system, we show that suppression of canonical Wnt signalling leads to a dose-dependent inhibition of supernumerary placodes in K14-Eda tissue explants.

Indexed as

AnimalsCell DifferentiationEctodysplasinsEmbryo, MammalianGene Expression Regulation, DevelopmentalHair FollicleHumansMammary Glands, HumanMiceMorphogenesisNF-kappa BWnt Signaling PathwayEctodysplasinsNF-kappa B

Identifiers

PMID26581094
PMCPMC4651331
OpenAlexW2178991492

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.