Evidence map›Paper›PMID 25092657›Full record

ArticleThe Journal of cell biology2014

PDK1-mediated activation of MRCKα regulates directional cell migration and lamellipodia retraction.

Paolo Armando Gagliardi, Laura di Blasio, Alberto Puliafito, Giorgio Seano, Roberto Sessa, Federica Chianale, Thomas Leung, Federico Bussolino, Luca Primo

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

18 citing papers in PubMed, 43 citations in OpenAlex.

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  18. A novel small-molecule MRCK inhibitor blocks cancer cell invasion.Cell communication and signaling : CCS · 2014
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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

9 authors at 3 institutions in 2 countries.

Paolo Armando GagliardiDepartment of Oncology and Center for Molecular Systems Biology, University of Turin, Turin 10060, Italy Laboratory of Cell Migration, Candiolo Cancer Institute FPO-IRCCS, Candiolo 10060, Italy.
Laura di BlasioDepartment of Oncology and Center for Molecular Systems Biology, University of Turin, Turin 10060, Italy Laboratory of Cell Migration, Candiolo Cancer Institute FPO-IRCCS, Candiolo 10060, Italy.
Alberto PuliafitoDepartment of Oncology and Center for Molecular Systems Biology, University of Turin, Turin 10060, Italy Laboratory of Cell Migration, Candiolo Cancer Institute FPO-IRCCS, Candiolo 10060, Italy.
Giorgio SeanoDepartment of Oncology and Center for Molecular Systems Biology, University of Turin, Turin 10060, Italy Laboratory of Cell Migration, Candiolo Cancer Institute FPO-IRCCS, Candiolo 10060, Italy.
Roberto SessaDepartment of Oncology and Center for Molecular Systems Biology, University of Turin, Turin 10060, Italy Laboratory of Cell Migration, Candiolo Cancer Institute FPO-IRCCS, Candiolo 10060, Italy.
Federica ChianaleDepartment of Oncology and Center for Molecular Systems Biology, University of Turin, Turin 10060, Italy Laboratory of Cell Migration, Candiolo Cancer Institute FPO-IRCCS, Candiolo 10060, Italy.
Thomas LeungInstitute of Molecular and Cell Biology, A-STAR, Singapore 138673, Singapore.
Federico BussolinoDepartment of Oncology and Center for Molecular Systems Biology, University of Turin, Turin 10060, ItalyDepartment of Oncology and Center for Molecular Systems Biology, University of Turin, Turin 10060, Italy Laboratory of Cell Migration, Candiolo Cancer Institute FPO-IRCCS, Candiolo 10060, Italy.
Luca PrimoDepartment of Oncology and Center for Molecular Systems Biology, University of Turin, Turin 10060, ItalyDepartment of Oncology and Center for Molecular Systems Biology, University of Turin, Turin 10060, Italy Laboratory of Cell Migration, Candiolo Cancer Institute FPO-IRCCS, Candiolo 10060, Italy luca.primo@ircc.it.
Candiolo Cancer Institute · ITUniversity of Turin · ITAgency for Science, Technology and Research · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Directional cell migration is of paramount importance in both physiological and pathological processes, such as development, wound healing, immune response, and cancer invasion. Here, we report that 3-phosphoinositide-dependent kinase 1 (PDK1) regulates epithelial directional migration and invasion by binding and activating myotonic dystrophy kinase-related CDC42-binding kinase α (MRCKα). We show that the effect of PDK1 on cell migration does not involve its kinase activity but instead relies on its ability to bind membrane phosphatidylinositol (3,4,5)-trisphosphate. Upon epidermal growth factor (EGF) stimulation, PDK1 and MRCKα colocalize at the cell membrane in lamellipodia. We demonstrate that PDK1 positively modulates MRCKα activity and drives its localization within lamellipodia. Likewise, the retraction phase of lamellipodia is controlled by PDK1 through an MRCKα-dependent mechanism. In summary, we discovered a functional pathway involving PDK1-mediated activation of MRCKα, which links EGF signaling to myosin contraction and directional migration.

Indexed as

Cell MovementProtein Processing, Post-TranslationalCatalytic DomainCell MembraneEnzyme ActivationEpidermal Growth FactorHeLa CellsHumansMyotonin-Protein KinasePhosphorylationProtein BindingProtein Serine-Threonine KinasesProtein TransportPseudopodiaPyruvate Dehydrogenase Acetyl-Transferring KinaseCDC42BPA protein, humanEpidermal Growth FactorMyotonin-Protein KinasePDK1 protein, humanProtein Serine-Threonine KinasesPyruvate Dehydrogenase Acetyl-Transferring Kinase

Identifiers

PMID25092657
PMCPMC4121984
OpenAlexW2159604123

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.