Evidence map›Paper›PMID 29784918›Full record

ArticleNature cell biology2018

Early lineage segregation of multipotent embryonic mammary gland progenitors.

Aline Wuidart, Alejandro Sifrim, Marco Fioramonti, Shigeru Matsumura, Audrey Brisebarre, Daniel Brown, Alessia Centonze, Anne Dannau, Christine Dubois, Alexandra Van Keymeulen and 2 more

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Nature cell biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 100 papers.

0numbers the graph read from it
0cells of the map it votes in
100citing papers in PubMed
8.7field-weighted citation impact, top 1% 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

100 citing papers in PubMed, 163 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. LMO2 Regulates Epithelial-Mesenchymal Plasticity of Mammary Epithelial Cells.Journal of mammary gland biology and neoplasia · 2026
    Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. [Application progress of single-cell RNA sequencing technology in breast development and related diseases].Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2025
    Review
  13. CXCR4Nature communications · 2025
    Article
  14. Article
  15. Article
  16. Article
  17. Mechanisms of Regulation of Cell Fate in Breast Development and Cancer.Advances in experimental medicine and biology · 2025
    Review
  18. Embryonic Mammary Gland Morphogenesis.Advances in experimental medicine and biology · 2025
    Review
  19. Article
  20. Review

40 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 2 countries.

Aline WuidartLaboratory of Stem Cells and Cancer, Université Libre de Bruxelles, Brussels, Belgium.
Alejandro SifrimDepartment of Human Genetics, University of Leuven, KU Leuven, Leuven, Belgium.
Marco FioramontiLaboratory of Stem Cells and Cancer, Université Libre de Bruxelles, Brussels, Belgium.
Shigeru MatsumuraLaboratory of Stem Cells and Cancer, Université Libre de Bruxelles, Brussels, Belgium.
Audrey BrisebarreLaboratory of Stem Cells and Cancer, Université Libre de Bruxelles, Brussels, Belgium.
Daniel BrownDepartment of Human Genetics, University of Leuven, KU Leuven, Leuven, Belgium.
Alessia CentonzeLaboratory of Stem Cells and Cancer, Université Libre de Bruxelles, Brussels, Belgium.
Anne DannauLaboratory of Stem Cells and Cancer, Université Libre de Bruxelles, Brussels, Belgium.
Christine DuboisLaboratory of Stem Cells and Cancer, Université Libre de Bruxelles, Brussels, Belgium.
Alexandra Van KeymeulenLaboratory of Stem Cells and Cancer, Université Libre de Bruxelles, Brussels, Belgium.
Thierry VoetDepartment of Human Genetics, University of Leuven, KU Leuven, Leuven, Belgium.
Cédric BlanpainLaboratory of Stem Cells and Cancer, Université Libre de Bruxelles, Brussels, Belgium. Cedric.Blanpain@ulb.ac.be.ORCID http://orcid.org/0000-0002-4028-4322
Université Libre de Bruxelles · BEWellcome Sanger Institute · GBKU Leuven · BE

Funding

European Research Council 616333
6 · The paper itself

Abstract

The mammary gland is composed of basal cells and luminal cells. It is generally believed that the mammary gland arises from embryonic multipotent progenitors, but it remains unclear when lineage restriction occurs and what mechanisms are responsible for the switch from multipotency to unipotency during its morphogenesis. Here, we perform multicolour lineage tracing and assess the fate of single progenitors, and demonstrate the existence of a developmental switch from multipotency to unipotency during embryonic mammary gland development. Molecular profiling and single cell RNA-seq revealed that embryonic multipotent progenitors express a unique hybrid basal and luminal signature and the factors associated with the different lineages. Sustained p63 expression in embryonic multipotent progenitors promotes unipotent basal cell fate and was sufficient to reprogram adult luminal cells into basal cells by promoting an intermediate hybrid multipotent-like state. Altogether, this study identifies the timing and the mechanisms mediating early lineage segregation of multipotent progenitors during mammary gland development.

Indexed as

Cell LineageAnimalsEpithelial CellsFemaleGene Expression ProfilingGene Expression Regulation, DevelopmentalGestational AgeMammary Glands, AnimalMiceMice, TransgenicMorphogenesisMouse Embryonic Stem CellsMultipotent Stem CellsPhenotypePhosphoproteinsSequence Analysis, RNAPhosphoproteinsTrans-ActivatorsTrp63 protein, mouse

Identifiers

PMID29784918
PMCPMC5985933
OpenAlexW2804088280

What OpenQuestion holds

Textmetadata
LicenceTDM
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.