Evidence map›Paper›PMID 30594912›Full record

ArticleAging2018

ΔNp63 promotes IGF1 signalling through IRS1 in squamous cell carcinoma.

Valentina Frezza, Claudia Fierro, Elena Gatti, Angelo Peschiaroli, Anna Maria Lena, Margherita Annicchiarico Petruzzelli, Eleonora Candi, Lucia Anemona, Alessandro Mauriello, Pier Giuseppe Pelicci and 2 more

Open access · greenAbstract read
In one paragraph

Article in Aging, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.8field-weighted citation impact, top 24% 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

10 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. TP63 Is Significantly Upregulated in Diabetic Kidney.International journal of molecular sciences · 2021
    Article
  7. Article
  8. Luteolin-7-International journal of molecular sciences · 2019
    Article
  9. Review
  10. Expression Profiles Reveal Involvement ofTechnology in cancer research & treatment
    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

12 authors at 5 institutions in 2 countries.

Valentina FrezzaDepartment of Experimental Medicine, TOR University of Rome "Tor Vergata", Rome 00133, Italy.
Claudia FierroDepartment of Experimental Medicine, TOR University of Rome "Tor Vergata", Rome 00133, Italy.
Elena GattiDepartment of Experimental Oncology European Institute of Oncology, Milan 20139, Italy.
Angelo PeschiaroliNational Research Council of Italy Institute of Translational Pharmacology (IFT-CNR), Rome 00133, Italy.
Anna Maria LenaDepartment of Experimental Medicine, TOR University of Rome "Tor Vergata", Rome 00133, Italy.
Margherita Annicchiarico PetruzzelliIstituto Dermopatico dell'Immacolata, IRCCS,, Rome 00163, Italy.
Eleonora CandiDepartment of Experimental Medicine, TOR University of Rome "Tor Vergata", Rome 00133, Italy.
Lucia AnemonaDepartment of Experimental Medicine, TOR University of Rome "Tor Vergata", Rome 00133, Italy.
Alessandro MaurielloDepartment of Experimental Medicine, TOR University of Rome "Tor Vergata", Rome 00133, Italy.
Pier Giuseppe PelicciDepartment of Experimental Oncology European Institute of Oncology, Milan 20139, Italy.
Gerry MelinoDepartment of Experimental Medicine, TOR University of Rome "Tor Vergata", Rome 00133, Italy.
Francesca BernassolaDepartment of Experimental Medicine, TOR University of Rome "Tor Vergata", Rome 00133, Italy.
University of Rome Tor Vergata · ITEuropean Institute of Oncology · ITIstituto Dermopatico dell'Immacolata · ITMedical Research Council · GBNational Research Council · IT

Funding

Medical Research Council MC_U132670600Medical Research Council MC_UU_00025/2
6 · The paper itself

Abstract

Accumulating evidence has proved that deregulation of ΔNp63 expression plays an oncogenic role in head and neck squamous cell carcinomas (HNSCCs). Besides p63, the type 1-insulin-like growth factor (IGF) signalling pathway has been implicated in HNSCC development and progression. Most insulin/IGF1 signalling converges intracellularly onto the protein adaptor insulin receptor substrate-1 (IRS-1) that transmits signals from the receptor to downstream effectors, including the PI3K/AKT and the MAPK kinase pathways, which, ultimately, promote proliferation, invasion, and cell survival. Here we report that p63 directly controls IRS1 transcription and cellular abundance and fosters the PI3K/AKT and MAPK downstream signalling pathways. Inactivation of ΔNp63 expression indeed reduces tumour cell responsiveness to IGF1 stimulation, and inhibits the growth potential of HNSCC cells. In addition, a positive correlation was observed between p63 and IRS1 expression in human HNSCC tissue arrays and in publicly available gene expression data. Our findings indicate that aberrant expression of ΔNp63 in HNSSC may act as an oncogenic stimulus by altering the IGF signalling pathway.

Indexed as

Carcinoma, Squamous CellCell Line, TumorGene Expression Regulation, NeoplasticHumansInsulinInsulin-Like Growth Factor IInsulin Receptor Substrate ProteinsMitogen-Activated Protein Kinase KinasesPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktTranscription FactorsTumor Suppressor ProteinsIGF1 protein, humanInsulinInsulin-Like Growth Factor IInsulin Receptor Substrate ProteinsIRS1 protein, humanMitogen-Activated Protein Kinase KinasesPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktTP63 protein, humanTranscription FactorsTumor Suppressor Proteinshead and neck tumoursIGF systemIRS1p53 familyp63

Identifiers

PMID30594912
PMCPMC6326668
OpenAlexW2907551482

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.