Evidence map›Paper›PMID 31591823›Full record

ArticleThe journal of pathology. Clinical research2020

∆Np63/p40 correlates with the location and phenotype of basal/mesenchymal cancer stem-like cells in human ER

Yajing Liu, Marta Nekulova, Rudolf Nenutil, Iva Horakova, M Virginia Appleyard, Karen Murray, Jitka Holcakova, Michaela Galoczova, Philip Quinlan, Lee B Jordan and 4 more

Open access · goldAbstract read
In one paragraph

Article in The journal of pathology. Clinical research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.4field-weighted citation impact, top 16% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. The metabolic profiles of cancer stem cells.Stem cell research & therapy · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. The dual role of p63 in cancer.Frontiers in oncology · 2023
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. 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

14 authors at 6 institutions in 3 countries.

Yajing LiuNCRC, University of Michigan, Ann Arbor, MI, USA.
Marta NekulovaRegional Centre for Applied Molecular Oncology, Masaryk Memorial Cancer Institute, Brno, Czech Republic.
Rudolf NenutilRegional Centre for Applied Molecular Oncology, Masaryk Memorial Cancer Institute, Brno, Czech Republic.
Iva HorakovaRegional Centre for Applied Molecular Oncology, Masaryk Memorial Cancer Institute, Brno, Czech Republic.
M Virginia AppleyardDundee Cancer Centre, University of Dundee, Ninewells Hospital and Medical School, Dundee, UK.
Karen MurrayDundee Cancer Centre, University of Dundee, Ninewells Hospital and Medical School, Dundee, UK.
Jitka HolcakovaRegional Centre for Applied Molecular Oncology, Masaryk Memorial Cancer Institute, Brno, Czech Republic.
Michaela GaloczovaRegional Centre for Applied Molecular Oncology, Masaryk Memorial Cancer Institute, Brno, Czech Republic.
Philip QuinlanAdvanced Data Analysis Centre, University of Nottingham, Nottingham, UK.
Lee B JordanDepartment of Pathology, Ninewells Hospital and Medical School, Dundee, UK.
Colin A PurdieDepartment of Pathology, Ninewells Hospital and Medical School, Dundee, UK.
Borivoj VojtesekRegional Centre for Applied Molecular Oncology, Masaryk Memorial Cancer Institute, Brno, Czech Republic.
Alastair M ThompsonDivision of Surgical Oncology, Dan L Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX, USA.
Philip J CoatesRegional Centre for Applied Molecular Oncology, Masaryk Memorial Cancer Institute, Brno, Czech Republic.ORCID 0000-0003-1518-6306
Masaryk Memorial Cancer Institute · CZNinewells Hospital · GBUniversity of Dundee · GBBaylor College of Medicine · USUniversity of Michigan · USUniversity of Nottingham · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ΔNp63, also known as p40, regulates stemness of normal mammary gland epithelium and provides stem cell characteristics in basal and HER2-driven murine breast cancer models. Whilst ΔNp63/p40 is a characteristic feature of normal basal cells and basal-type triple-negative breast cancer, some receptor-positive breast cancers express ΔNp63/p40 and its overexpression imparts cancer stem cell-like properties in ER

Indexed as

AnimalsBiomarkers, TumorBreast NeoplasmsErb-b2 Receptor Tyrosine KinasesFemaleHeterograftsHumansMiceNeoplastic Stem CellsPhenotypeReceptors, EstrogenTranscription FactorsTumor Suppressor ProteinsBiomarkers, TumorERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesReceptors, EstrogenTP63 protein, humanTranscription FactorsTumor Suppressor Proteinsaldehyde dehydrogenasebreastcancer stem cellsCD44HER2oestrogen receptorp40p63ΔNp63

Identifiers

PMID31591823
PMCPMC6966710
OpenAlexW2980297352

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.