Evidence map›Paper›PMID 25101116›Full record

ArticleFrontiers in genetics2014

ARF: a versatile DNA damage response ally at the crossroads of development and tumorigenesis.

Athanassios Kotsinas, Panagiota Papanagnou, Konstantinos Evangelou, George C Trigas, Vassiliki Kostourou, Paul Townsend, Vassilis G Gorgoulis

Open access · goldAbstract read
In one paragraph

Article in Frontiers in genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

11 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Insights into the regulation of neuronal viability by nucleophosmin/B23.Experimental biology and medicine (Maywood, N.J.) · 2015
    Review
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 2 countries.

Athanassios KotsinasMolecular Carcinogenesis Group, Department of Histology and Embryology, School of Medicine, University of Athens Athens, Greece.
Panagiota PapanagnouMolecular Carcinogenesis Group, Department of Histology and Embryology, School of Medicine, University of Athens Athens, Greece.
Konstantinos EvangelouMolecular Carcinogenesis Group, Department of Histology and Embryology, School of Medicine, University of Athens Athens, Greece.
George C TrigasMolecular Carcinogenesis Group, Department of Histology and Embryology, School of Medicine, University of Athens Athens, Greece.
Vassiliki KostourouVascular Adhesion Lab, Biomedical Sciences Research Center Alexander Fleming Athens, Greece.
Paul TownsendFaculty Institute of Cancer Sciences, University of Manchester, Manchester Academic Health Science Centre Manchester, UK ; Manchester Centre for Cellular Metabolism, University of Manchester, Manchester Academic Health Science Centre Manchester, UK.
Vassilis G GorgoulisMolecular Carcinogenesis Group, Department of Histology and Embryology, School of Medicine, University of Athens Athens, Greece ; Faculty Institute of Cancer Sciences, University of Manchester, Manchester Academic Health Science Centre Manchester, UK ; Manchester Centre for Cellular Metabolism, University of Manchester, Manchester Academic Health Science Centre Manchester, UK ; Biomedical Research Foundation, Academy of Athens Athens, Greece.
National and Kapodistrian University of Athens · GRAcademy of Athens · GRAlexander Fleming Biomedical Sciences Research Center · GRUniversity of Manchester · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alternative reading frame (ARF) is a tumor suppressor protein that senses oncogenic and other stressogenic signals. It can trigger p53-dependent and -independent responses with cell cycle arrest and apoptosis induction being the most prominent ones. Other ARF activities, particularly p53-independent ones, that could help in understanding cancer development and provide potential therapeutic exploitation are underrated. Although ARF is generally not expressed in normal tissues, it is essential for ocular and male germ cells development. The underlying mechanism(s) in these processes, while not clearly defined, point toward a functional link between ARF, DNA damage and angiogenesis. Based on a recent study from our group demonstrating a functional interplay between ataxia-telangiectasia mutated (ATM) and ARF during carcinogenesis, we discuss the role of ARF at the crossroads of cancer and developmental processes.

Indexed as

angiogenesisARFATMinvolutionmeiosisocular developmentspermatogenesisvascular network

Identifiers

PMID25101116
PMCPMC4106421
OpenAlexW2068219524

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.