Evidence map›Paper›PMID 23851489›Full record

ArticleNature cell biology2013

Functional interplay between the DNA-damage-response kinase ATM and ARF tumour suppressor protein in human cancer.

Georgia Velimezi, Michalis Liontos, Konstantinos Vougas, Theodoros Roumeliotis, Jirina Bartkova, Maria Sideridou, Ayguel Dereli-Oz, Maciej Kocylowski, Ioannis S Pateras, Kostas Evangelou and 13 more

Erratum issuedAbstract read
PubMed Publisher
In one paragraph

Article in Nature cell biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed
10.0field-weighted citation impact, top 1% 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

80 citing papers in PubMed, 129 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. SIRT7 promotes lung cancer progression by destabilizing the tumor suppressor ARF.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
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  6. Review
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  8. Article
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  12. Mesenchymal Stem Cell Senescence and Osteogenesis.Medicina (Kaunas, Lithuania) · 2021
    Review
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  14. Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
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20 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

23 authors at 9 institutions in 7 countries.

Georgia VelimeziMolecular Carcinogenesis Group, Department of Histology and Embryology, School of Medicine, University of Athens, 75 Mikras Asias Str, Athens, GR-11527, Greece.
Michalis Liontos
Konstantinos Vougas
Theodoros Roumeliotis
Jirina Bartkova
Maria Sideridou
Ayguel Dereli-Oz
Maciej Kocylowski
Ioannis S Pateras
Kostas Evangelou
Athanassios Kotsinas
Ines Orsolic
Sladana Bursac
Maja Cokaric-Brdovcak
Vassilis Zoumpourlis
Dimitris Kletsas
George Papafotiou
Apostolos Klinakis
Sinisa Volarevic
Wei Gu
Jiri Bartek
Thanos D Halazonetis
Vassilis G Gorgoulis
National and Kapodistrian University of Athens · GRUniversity of Rijeka · HRBiomedical Research Foundation of the Academy of Athens · GRDanish Cancer Society · DKAcademy of Athens · GRUniversity of Geneva · CHColumbia University · USInstitute of Biosciences & ApplicationsNational Hellenic Research Foundation · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The DNA damage response (DDR) pathway and ARF function as barriers to cancer development. Although commonly regarded as operating independently of each other, some studies proposed that ARF is positively regulated by the DDR. Contrary to either scenario, we found that in human oncogene-transformed and cancer cells, ATM suppressed ARF protein levels and activity in a transcription-independent manner. Mechanistically, ATM activated protein phosphatase 1, which antagonized Nek2-dependent phosphorylation of nucleophosmin (NPM), thereby liberating ARF from NPM and rendering it susceptible to degradation by the ULF E3-ubiquitin ligase. In human clinical samples, loss of ATM expression correlated with increased ARF levels and in xenograft and tissue culture models, inhibition of ATM stimulated the tumour-suppressive effects of ARF. These results provide insights into the functional interplay between the DDR and ARF anti-cancer barriers, with implications for tumorigenesis and treatment of advanced tumours.

Indexed as

ADP-Ribosylation Factor 1AnimalsAtaxia Telangiectasia Mutated ProteinsCarrier ProteinsCell CycleCell Cycle ProteinsCell LineCell Line, TumorDNA-Binding ProteinsGene Expression Regulation, NeoplasticHeLa CellsHumansMaleMiceNeoplasmsNIMA-Related KinasesADP-Ribosylation Factor 1Ataxia Telangiectasia Mutated ProteinsATM protein, humanAtm protein, mouseCarrier ProteinsCell Cycle ProteinsDNA-Binding ProteinsNEK2 protein, humanNIMA-Related KinasesProtein Serine-Threonine KinasesTRIP12 protein, humanTumor Suppressor Protein p14ARFUbiquitin-Protein Ligases

Identifiers

PMID23851489
OpenAlexW2039467788

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.