Evidence map›Paper›PMID 29233040›Full record

ArticleCell cycle (Georgetown, Tex.)2018

Integrin-β4 is a novel transcriptional target of TAp73.

Ningxia Xie, Polina Vikhreva, Margherita Annicchiarico-Petruzzelli, Ivano Amelio, Nicolai Barlev, Richard A Knight, Gerry Melino

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.1field-weighted citation impact, top 20% 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

16 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. p73 as a Tissue Architect.Frontiers in cell and developmental biology · 2021
    Review
  8. Review
  9. Review
  10. Skin immunity and its dysregulation in psoriasis.Cell cycle (Georgetown, Tex.) · 2019
    Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. 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

7 authors at 4 institutions in 3 countries.

Ningxia Xiea MRC Toxicology Unit , Hodgkin Building , Lancaster Road, Leicester LE1 9HN , United Kingdom.
Polina Vikhrevaa MRC Toxicology Unit , Hodgkin Building , Lancaster Road, Leicester LE1 9HN , United Kingdom.
Margherita Annicchiarico-Petruzzellic Biochemistry Laboratory , IDI-IRCCS , Rome 00133 , Italy.
Ivano Amelioa MRC Toxicology Unit , Hodgkin Building , Lancaster Road, Leicester LE1 9HN , United Kingdom.
Nicolai Barlevd Institute of Cytology Russian Academy of Sciences , Saint-Petersburg , 194064 , Russia.
Richard A Knighta MRC Toxicology Unit , Hodgkin Building , Lancaster Road, Leicester LE1 9HN , United Kingdom.ORCID 0000-0003-2985-7764
Gerry Melinoa MRC Toxicology Unit , Hodgkin Building , Lancaster Road, Leicester LE1 9HN , United Kingdom.
MRC Toxicology Unit · GBUniversity of Rome Tor Vergata · ITInstitute of Cytology · RUIstituti di Ricovero e Cura a Carattere Scientifico · IT

Funding

Medical Research Council MC_U132670600
6 · The paper itself

Abstract

As a member of p53 family, p73 has attracted intense investigations due to its structural and functional similarities to p53. Among more than ten p73 variants, the transactivation (TA) domain-containing isoform TAp73 is the one that imitates the p53's behavior most. TAp73 induces apoptosis and cell cycle arrest, which endows it the capacity of tumour suppression. Also, it can exert diverse biological influences on cells through activating a complex and context dependent transcriptional programme. The transcriptional activities further broaden its roles in more intricate biological processes. In this article, we report that p73 is a positive regulator of a cell adhesion related gene named integrin β4 (ITGB4). This finding may have implications for the dissection of the biological mechanisms underlining p73 functions.

Indexed as

Transcription, GeneticCell Cycle CheckpointsCell Line, TumorCyclin-Dependent Kinase Inhibitor p21HEK293 CellsHumansIntegrin beta4Promoter Regions, GeneticProtein BindingTransfectionTumor Protein p73Cyclin-Dependent Kinase Inhibitor p21Integrin beta4Tumor Protein p73adhesion and migrationcancer cellscell interactionIntegrinsoncogenes and tumor suppressorsoncosupressionp53 familyp73transcription factors

Identifiers

PMID29233040
PMCPMC5969564
OpenAlexW2774015416

What Socratic 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 Socratic graph.