Evidence map›Paper›PMID 21643019›Full record

ArticleOncogene2011

TP63 P2 promoter functional analysis identifies β-catenin as a key regulator of ΔNp63 expression.

C Ruptier, A De Gaspéris, S Ansieau, A Granjon, P Tanière, I Lafosse, H Shi, A Petitjean, E Taranchon-Clermont, V Tribollet and 7 more

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

23 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. A simple method to generate human airway epithelial organoids with externally orientated apical membranes.American journal of physiology. Lung cellular and molecular physiology · 2022
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. A 'tad' of hope in the fight against airway disease.Biochemical Society transactions · 2020
    Review
  11. Article
  12. Article
  13. IL-1β Inflammatory Cytokine-InducedInternational journal of molecular sciences · 2019
    Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. ASPP2 suppresses squamous cell carcinoma via RelA/p65-mediated repression of p63.Proceedings of the National Academy of Sciences of the United States of America · 2013
    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

17 authors at 4 institutions in 1 country.

C RuptierUniversité de Lyon, Lyon, France.
A De Gaspéris
S Ansieau
A Granjon
P Tanière
I Lafosse
H Shi
A Petitjean
E Taranchon-Clermont
V Tribollet
T Voeltzel
J-Y Scoazec
V Maguer-Satta
A Puisieux
P Hainaut
C Cavard
C Caron de Fromentel
Université Claude Bernard Lyon 1 · FRCentre International de Recherche sur le Cancer · FRCentre National de la Recherche Scientifique · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ΔNp63 protein, a product of the TP63 gene that lacks the N-terminal domain, has a critical role in the maintenance of self renewal and progenitor capacity in several types of epithelial tissues. ΔNp63 is frequently overexpressed in squamous cell carcinoma (SCC) and in some other epithelial tumours. This overexpression may contribute to tumour progression through dominant-negative effects on the transcriptionally active (TA) isoforms of the p53 family (TAp63, TAp73 and p53), as well as through independent mechanisms. However, the molecular basis of ΔNp63 overexpression is not fully understood. Here, we show that the expression of ΔNp63 is regulated by the Wnt/β-catenin pathway in human hepatocellular carcinoma (HCC) and SCC cell lines. This regulation operates in particular through TCF/LEF sites present in the P2 promoter of TP63. In addition, we show that ΔNp63 and β-catenin are frequently coexpressed and accumulated in oesophageal SCC, but not in HCC. These results suggest that activation of the β-catenin pathway may contribute to overexpression of ΔNp63 during tumour progression, in a cell type-specific manner.

Indexed as

beta CateninCarcinoma, HepatocellularCarcinoma, Squamous CellCell Line, TumorEsophageal NeoplasmsGene Expression Regulation, NeoplasticHumansLiver NeoplasmsPromoter Regions, GeneticProtein IsoformsSignal TransductionTranscription FactorsTumor Suppressor Protein p53Tumor Suppressor Proteinsbeta CateninProtein IsoformsTP63 protein, humanTranscription FactorsTumor Suppressor Protein p53Tumor Suppressor Proteins

Identifiers

PMID21643019
OpenAlexW2083308534

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.