Evidence map›Paper›PMID 28436949›Full record

ArticleOncogene2017

p14ARF interacts with the focal adhesion kinase and protects cells from anoikis.

M Vivo, R Fontana, M Ranieri, G Capasso, T Angrisano, A Pollice, V Calabrò, G La Mantia

Open access · hybridAbstract read
In one paragraph

Article in Oncogene, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

27 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
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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 1 institution in 1 country.

M VivoDipartimento di Biologia, Università Degli Studi di Napoli 'Federico II', Napoli, Italy.ORCID 0000-0003-2458-4226
R FontanaDipartimento di Biologia, Università Degli Studi di Napoli 'Federico II', Napoli, Italy.
M RanieriDipartimento di Biologia, Università Degli Studi di Napoli 'Federico II', Napoli, Italy.
G CapassoDipartimento di Biologia, Università Degli Studi di Napoli 'Federico II', Napoli, Italy.
T AngrisanoDipartimento di Biologia, Università Degli Studi di Napoli 'Federico II', Napoli, Italy.
A PolliceDipartimento di Biologia, Università Degli Studi di Napoli 'Federico II', Napoli, Italy.
V CalabròDipartimento di Biologia, Università Degli Studi di Napoli 'Federico II', Napoli, Italy.
G La MantiaDipartimento di Biologia, Università Degli Studi di Napoli 'Federico II', Napoli, Italy.
University of Naples Federico II · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ARF protein functions as an important sensor of hyper-proliferative stimuli restricting cell proliferation through both p53-dependent and -independent pathways. Although to date the majority of studies on ARF have focused on its anti-proliferative role, few studies have addressed whether ARF may also have pro-survival functions. Here we show for the first time that during the process of adhesion and spreading ARF re-localizes to sites of active actin polymerization and to focal adhesion points where it interacts with the phosphorylated focal adhesion kinase. In line with its recruitment to focal adhesions, we observe that hampering ARF function in cancer cells leads to gross defects in cytoskeleton organization resulting in apoptosis through a mechanism dependent on the Death-Associated Protein Kinase. Our data uncover a novel function for p14ARF in protecting cells from anoikis that may reflect its role in anchorage independence, a hallmark of malignant tumor cells.

Indexed as

AnoikisApoptosisCell AdhesionCell Line, TumorCell ProliferationCell SurvivalCytoskeletonDeath-Associated Protein KinasesFocal Adhesion Protein-Tyrosine KinasesFocal AdhesionsHeLa CellsHumansMCF-7 CellsPhosphorylationSignal TransductionTumor Suppressor Protein p14ARFDeath-Associated Protein KinasesFocal Adhesion Protein-Tyrosine KinasesTumor Suppressor Protein p14ARF

Identifiers

PMID28436949
PMCPMC5582215
OpenAlexW2608424556

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.