Evidence map›Paper›PMID 25924946›Full record

ArticleBMC cancer2015

PKCα promotes the mesenchymal to amoeboid transition and increases cancer cell invasiveness.

Katarína Vaškovičová, Emilia Szabadosová, Vladimír Čermák, Aneta Gandalovičová, Lenka Kasalová, Daniel Rösel, Jan Brábek

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

8 citing papers in PubMed, 13 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

7 authors at 2 institutions in 1 country.

Katarína VaškovičováDepartment of Cell Biology, Laboratory of Cancer Cell Invasion, Charles University in Prague, Prague, Czech Republic. katarina.vaskovicova@gmail.com.
Emilia SzabadosováDepartment of Cell Biology, Laboratory of Cancer Cell Invasion, Charles University in Prague, Prague, Czech Republic. emiluska@gmail.com.
Vladimír ČermákDepartment of Cell Biology, Laboratory of Cancer Cell Invasion, Charles University in Prague, Prague, Czech Republic. cermak@natur.cuni.cz.
Aneta GandalovičováDepartment of Cell Biology, Laboratory of Cancer Cell Invasion, Charles University in Prague, Prague, Czech Republic. gandaloa@natur.cuni.cz.
Lenka KasalováDepartment of Cell Biology, Laboratory of Cancer Cell Invasion, Charles University in Prague, Prague, Czech Republic. kasalova@biotech.cz.
Daniel RöselDepartment of Cell Biology, Laboratory of Cancer Cell Invasion, Charles University in Prague, Prague, Czech Republic. rosel@natur.cuni.cz.
Jan BrábekDepartment of Cell Biology, Laboratory of Cancer Cell Invasion, Charles University in Prague, Prague, Czech Republic. brabek@natur.cuni.cz.
Charles University · CZCzech Academy of Sciences · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe local invasion of tumor cells into the surrounding tissue is the first and most critical step of the metastatic cascade. Cells can invade either collectively, or individually. Individual cancer cell invasion can occur in the mesenchymal or amoeboid mode, which are mutually interchangeable. This plasticity of individual cancer cell invasiveness may represent an escape mechanism for invading cancer cells from anti-metastatic treatment.

methodsTo identify new signaling proteins involved in the plasticity of cancer cell invasiveness, we performed proteomic analysis of the amoeboid to mesenchymal transition with A375m2 melanoma cells in a 3D Matrigel matrix.

resultsIn this screen we identified PKCα as an important protein for the maintenance of amoeboid morphology. We found that the activation of PKCα resulted in the mesenchymal-amoeboid transition of mesenchymal K2 and MDA-MB-231 cell lines. Consistently, PKCα inhibition led to the amoeboid-mesenchymal transition of amoeboid A375m2 cells. Next, we showed that PKCα inhibition resulted in a considerable decrease in the invading abilities of all analyzed cancer cell lines.

conclusionsOur results suggest that PKCα is an important protein for maintenance of the amoeboid morphology of cancer cells, and that downregulation of PKCα results in the amoeboid to mesenchymal transition. Our data also suggest that PKCα is important for both mesenchymal and amoeboid invasiveness, making it an attractive target for anti-metastatic therapies.

Indexed as

Cell Line, TumorCell MovementGene Expression Regulation, NeoplasticHumansMelanomaMesodermNeoplasm InvasivenessProtein Kinase C-alphaProteomicsSignal TransductionPRKCA protein, humanProtein Kinase C-alpha

Identifiers

PMID25924946
PMCPMC4423130
OpenAlexW1975485465

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.