Evidence map›Paper›PMID 23382862›Full record

ArticlePloS one2013

P-Rex1 cooperates with PDGFRβ to drive cellular migration in 3D microenvironments.

Andrew D Campbell, Samuel Lawn, Lynn C McGarry, Heidi C Welch, Bradford W Ozanne, Jim C Norman

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
4.0field-weighted citation impact, top 6% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

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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

6 authors at 2 institutions in 1 country.

Andrew D CampbellBeatson Institute for Cancer Research, Bearsden, Glasgow, United Kingdom.
Samuel Lawn
Lynn C McGarry
Heidi C Welch
Bradford W Ozanne
Jim C Norman
Cancer Research UK Scotland Institute · GBBabraham Institute · GB

Funding

Biotechnology and Biological Sciences Research Council BBS/E/B/000C0411Cancer Research UK
6 · The paper itself

Abstract

Expression of the Rac-guanine nucleotide exchange factor (RacGEF), P-Rex1 is a key determinant of progression to metastasis in a number of human cancers. In accordance with this proposed role in cancer cell invasion and metastasis, we find that ectopic expression of P-Rex1 in an immortalised human fibroblast cell line is sufficient to drive multiple migratory and invasive phenotypes. The invasive phenotype is greatly enhanced by the presence of a gradient of serum or platelet-derived growth factor, and is dependent upon the expression of functional PDGF receptor β. Consistently, the invasiveness of WM852 melanoma cells, which endogenously express P-Rex1 and PDGFRβ, is opposed by siRNA of either of these proteins. Furthermore, the current model of P-Rex1 activation is advanced through demonstration of P-Rex1 and PDGFRβ as components of the same macromolecular complex. These data suggest that P-Rex1 has an influence on physiological migratory processes, such as invasion of cancer cells, both through effects upon classical Rac1-driven motility and a novel association with RTK signalling complexes.

Indexed as

MelanomaCell Line, TumorCell MovementFibroblastsGene Expression Regulation, NeoplasticGuanine Nucleotide Exchange FactorsHumansMacromolecular SubstancesNeoplasm InvasivenessNeoplasm MetastasisReceptor, Platelet-Derived Growth Factor betaRNA, Small InterferingTumor MicroenvironmentGuanine Nucleotide Exchange FactorsMacromolecular SubstancesPREX1 protein, humanReceptor, Platelet-Derived Growth Factor betaRNA, Small Interfering

Identifiers

PMID23382862
PMCPMC3559689
OpenAlexW2028510625

What OpenQuestion holds

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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.