Evidence map›Paper›PMID 24127607›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2013

ASPP2 suppresses squamous cell carcinoma via RelA/p65-mediated repression of p63.

Luca Tordella, Sofia Koch, Victoria Salter, Anna Pagotto, Jessica B Doondeea, Stephan M Feller, Indrika Ratnayaka, Shan Zhong, Robert D Goldin, Guillermina Lozano and 7 more

Open access · hybridAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

37 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. FIH-1 engages novel binding partners to positively influence epithelial proliferation via p63.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2020
    Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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 6 institutions in 3 countries.

Luca TordellaLudwig Institute for Cancer Research, Nuffield Department of Clinical Medicine, and Weatherall Institute of Molecular Medicine, University of Oxford, Oxford OX3 7DQ, United Kingdom.
Sofia Koch
Victoria Salter
Anna Pagotto
Jessica B Doondeea
Stephan M Feller
Indrika Ratnayaka
Shan Zhong
Robert D Goldin
Guillermina Lozano
Frank D McKeon
Mahvash Tavassoli
Florian Fritzsche
Gerhard F Huber
Matthias Rössle
Holger Moch
Xin Lu
University of Oxford · GBHarvard University · USImperial College London · GBKing's College London · GBThe University of Texas MD Anderson Cancer Center · USUniversity Hospital of Zurich · CH

Funding

Cancer Research UKMedical Research Council MR/J000930/1
6 · The paper itself

Abstract

Squamous cell carcinoma (SCC) is highly malignant and refractory to therapy. The majority of existing mouse SCC models involve multiple gene mutations. Very few mouse models of spontaneous SCC have been generated by a single gene deletion. Here we report a haploinsufficient SCC mouse model in which exon 3 of the Tp53BP2 gene (a p53 binding protein) was deleted in one allele in a BALB/c genetic background. Tp53BP2 encodes ASPP2 (ankyrin repeats, SH3 domain and protein rich region containing protein 2). Keratinocyte differentiation induces ASPP2 and its expression is inversely correlated with p63 protein in vitro and in vivo. Up-regulation of p63 expression is required for ASPP2(Δexon3/+) BALB/c mice to develop SCC, as heterozygosity of p63 but not p53 prevents them from developing it. Mechanistically, ASPP2 inhibits ΔNp63 expression through its ability to bind IκB and enhance nuclear Rel/A p65, a component of the NF-κB transcription complex, which mediates the repression of p63. Reduced ASPP2 expression associates with tumor metastasis and increased p63 expression in human head and neck SCCs. This study identifies ASPP2 as a tumor suppressor that suppresses SCC via inflammatory signaling through NF-κB-mediated repression of p63.

Indexed as

Disease Models, AnimalAnimalsCarcinoma, Squamous CellCell LineCrosses, GeneticDNA PrimersHaploinsufficiencyHumansImmunoblottingImmunoprecipitationMiceMice, Inbred BALB CMicroarray AnalysisPhosphoproteinsReal-Time Polymerase Chain ReactionRNA, Small InterferingDNA PrimersPhosphoproteinsRela protein, mouseRNA, Small InterferingTrans-ActivatorsTranscription Factor RelATrp53bp2 protein, mouseTrp63 protein, mouseTumor Suppressor Proteinsinflammationstratified epithelial cell tumorT53BP2

Identifiers

PMID24127607
PMCPMC3816480
OpenAlexW2170979457

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.