Evidence map›Paper›PMID 19331830›Full record

ArticleExperimental cell research2009

Residues in the alternative reading frame tumor suppressor that influence its stability and p53-independent activities.

Anne di Tommaso, Jussara Hagen, Van Tompkins, Viviane Muniz, Amel Dudakovic, Alain Kitzis, Veronique Ladeveze, Dawn E Quelle

Open access · greenAbstract read
In one paragraph

Article in Experimental cell research, 2009. 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
1.0field-weighted citation impact, top 23% 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, 24 citations in OpenAlex.

  1. NovelCold Spring Harbor molecular case studies · 2019
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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

8 authors at 3 institutions in 2 countries.

Anne di TommasoPole Biologie Sante, UMR 6187 CNRS, Pathologies Moléculaire de l'Adressage et de la Signalisation, Université de Poitiers, Poitiers, France.
Jussara Hagen
Van Tompkins
Viviane Muniz
Amel Dudakovic
Alain Kitzis
Veronique Ladeveze
Dawn E Quelle
University of Iowa · USCentre National de la Recherche Scientifique · FRUniversité de Poitiers · FR

Funding

Growth Inhibition by the ARF Tumor SuppressorR01CA090367 · NCI · UNIVERSITY OF IOWA · PI QUELLE, DAWN E · 2002 to 2011
$2.9M
NCI NIH HHS R01 CA090367
6 · The paper itself

Abstract

The Alternative Reading Frame (ARF) protein suppresses tumorigenesis through p53-dependent and p53-independent pathways. Most of ARF's anti-proliferative activity is conferred by sequences in its first exon. Previous work showed specific amino acid changes occurred in that region during primate evolution, so we programmed those changes into human p14ARF to assay their functional impact. Two human p14ARF residues (Ala(14) and Thr(31)) were found to destabilize the protein while two others (Val(24) and Ala(41)) promoted more efficient p53 stabilization and activation. Despite those effects, all modified p14ARF forms displayed robust p53-dependent anti-proliferative activity demonstrating there are no significant biological differences in p53-mediated growth suppression associated with simian versus human p14ARF residues. In contrast, p53-independent p14ARF function was considerably altered by several residue changes. Val(24) was required for p53-independent growth suppression whereas multiple residues (Val(24), Thr(31), Ala(41) and His(60)) enabled p14ARF to block or reverse the inherent chromosomal instability of p53-null MEFs. Together, these data pinpoint specific residues outside of established p14ARF functional domains that influence its expression and signaling activities. Most intriguingly, this work reveals a novel and direct role for p14ARF in the p53-independent maintenance of genomic stability.

Indexed as

Genomic InstabilityAmino Acid SequenceAnimalsCell LineFibroblastsGenes, ReporterHumansMiceMice, KnockoutMolecular Sequence DataPrimatesTumor Suppressor Protein p14ARFTumor Suppressor Protein p53Tumor Suppressor Protein p14ARFTumor Suppressor Protein p53

Identifiers

PMID19331830
PMCPMC2665200
OpenAlexW2003525320

What OpenQuestion holds

Textmetadata
LicenceTDM
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.