Evidence map›Paper›PMID 28361970›Full record

ArticleScientific reports2017

PCTK3/CDK18 regulates cell migration and adhesion by negatively modulating FAK activity.

Shinya Matsuda, Kohei Kawamoto, Kenji Miyamoto, Akihiko Tsuji, Keizo Yuasa

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

15 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
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  7. Molecular cancer therapeutics · 2020
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  15. Characterization of the role of RILP in cell migration.European journal of histochemistry : EJH · 2017
    Article
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

5 authors at 1 institution in 1 country.

Shinya MatsudaDepartment of Biological Science and Technology, Tokushima University Graduate School, Minamijosanjima, Tokushima 770-8506, Japan.
Kohei KawamotoDepartment of Biological Science and Technology, Tokushima University Graduate School, Minamijosanjima, Tokushima 770-8506, Japan.
Kenji MiyamotoDepartment of Biological Science and Technology, Tokushima University Graduate School, Minamijosanjima, Tokushima 770-8506, Japan.
Akihiko TsujiDepartment of Biological Science and Technology, Tokushima University Graduate School, Minamijosanjima, Tokushima 770-8506, Japan.
Keizo YuasaDepartment of Biological Science and Technology, Tokushima University Graduate School, Minamijosanjima, Tokushima 770-8506, Japan.
Tokushima University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PCTAIRE kinase 3 (PCTK3) is a member of the cyclin dependent kinase family, but its physiological function remains unknown. We previously reported that PCTK3-knockdown HEK293T cells showed actin accumulation at the leading edge, suggesting that PCTK3 is involved in the regulation of actin reorganization. In this study, we investigated the physiological function and downstream signal transduction molecules of PCTK3. PCTK3 knockdown in HEK293T cells increased cell motility and RhoA/Rho-associated kinase activity as compared with control cells. We also found that phosphorylation at residue Tyr-397 in focal adhesion kinase (FAK) was increased in PCTK3-knockdown cells. FAK phosphorylation at Tyr-397 was increased in response to fibronectin stimulation, whereas its phosphorylation was suppressed by PCTK3. In addition, excessive expression of PCTK3 led to the formation of filopodia during the early stages of cell adhesion in HeLa cells. These results indicate that PCTK3 controls actin cytoskeleton dynamics by negatively regulating the FAK/Rho signaling pathway.

Indexed as

Actin CytoskeletonActinsCell AdhesionCell LineCell Line, TumorCell MovementCyclin-Dependent KinasesFocal Adhesion Kinase 1Focal Adhesion Protein-Tyrosine KinasesHEK293 CellsHeLa CellsHumansPhosphorylationProtein-Tyrosine KinasesPseudopodiarhoA GTP-Binding ProteinActinsCyclin-Dependent KinasesFocal Adhesion Kinase 1Focal Adhesion Protein-Tyrosine KinasesPCTAIRE-3 protein kinaseProtein-Tyrosine KinasesPTK2 protein, humanrhoA GTP-Binding Proteinrho-Associated Kinases

Identifiers

PMID28361970
PMCPMC5374530
OpenAlexW2599709405

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.