Evidence map›Paper›PMID 33168840›Full record

ArticleScientific reports2020

Genetic analyses in mouse fibroblast and melanoma cells demonstrate novel roles for PDGF-AB ligand and PDGF receptor alpha.

Julie L Kadrmas, Mary C Beckerle, Masaaki Yoshigi

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

9 citing papers in PubMed, 19 citations in OpenAlex.

  1. EnhancedSkin health and disease · 2026
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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

3 authors at 1 institution in 1 country.

Julie L KadrmasHuntsman Cancer Institute, The University of Utah, Salt Lake City, UT, 84112, USA. julie.kadrmas@hci.utah.edu.
Mary C BeckerleHuntsman Cancer Institute, The University of Utah, Salt Lake City, UT, 84112, USA. mary.beckerle@hci.utah.edu.
Masaaki YoshigiDepartment of Pediatrics, The University of Utah, Salt Lake City, UT, 84112, USA. masaaki.yoshigi@hsc.utah.edu.
University of Utah · US

Funding

UTAH REGIONAL CANCER CENTERP30CA042014 · NCI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI KATHARINE S ULLMAN · 1986 to 2026
$72.6M
Structure and function of stress fibers and cell adhesion sitesR01GM050877 · NIGMS · UNIVERSITY OF UTAH · PI BECKERLE, MARY C. · 1994 to 2020
$7.8M
Mechanisms for regulation of cell adhesion and migrationR01GM084103 · NIGMS · UNIVERSITY OF UTAH · PI KADRMAS, JULIE L · 2009 to 2013
$1.4M
NCI NIH HHS P30 CA042014NIGMS NIH HHS R01 GM050877NIGMS NIH HHS R01 GM084103NIH HHS GM084103NIH HHS GM50867
6 · The paper itself

Abstract

Platelet Derived Growth Factor Receptor (PDGFR) signaling is a central mitogenic pathway in development, as well as tissue repair and homeostasis. The rules governing the binding of PDGF ligand to the receptor to produce activation and downstream signaling have been well defined over the last several decades. In cultured cells after a period of serum deprivation, treatment with PDGF leads to the rapid formation of dramatic, actin-rich Circular Dorsal Ruffles (CDRs). Using CDRs as a robust visual readout of early PDGFR signaling, we have identified several contradictory elements in the widely accepted model of PDGF activity. Employing CRISPR/Cas9 gene editing to disrupt the Pdgfra gene in two different murine cell lines, we show that in addition to the widely accepted function for PDGFR-beta in CDR formation, PDGFR-alpha is also clearly capable of eliciting CDRs. Moreover, we demonstrate activity for heterodimeric PDGF-AB ligand in the vigorous activation of PDGFR-beta homodimers to produce CDRs. These findings are key to a more complete understanding of PDGF ligand-receptor interactions and their downstream signaling consequences. This knowledge will allow for more rigorous experimental design in future studies of PDGFR signaling and its contributions to development and disease.

Indexed as

AnimalsBecaplerminCell Line, TumorCRISPR-Cas SystemsFibroblastsGene Expression Regulation, NeoplasticLigandsMelanomaMicePlatelet-Derived Growth FactorProtein BindingProtein MultimerizationReceptor, Platelet-Derived Growth Factor alphaSignal TransductionBecaplerminLigandsPlatelet-Derived Growth Factorplatelet-derived growth factor Aplatelet-derived growth factor ABReceptor, Platelet-Derived Growth Factor alpha

Identifiers

PMID33168840
PMCPMC7653911
OpenAlexW3098882801

What OpenQuestion holds

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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.