Evidence map›Paper›PMID 24967897›Full record

ArticlePloS one2014

Arp2/3 inhibition induces amoeboid-like protrusions in MCF10A epithelial cells by reduced cytoskeletal-membrane coupling and focal adhesion assembly.

Yvonne Beckham, Robert J Vasquez, Jonathan Stricker, Kareem Sayegh, Clement Campillo, Margaret L Gardel

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.7field-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

32 citing papers in PubMed, 47 citations in OpenAlex.

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  8. βCells · 2024
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  14. Review
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  18. Actin cytoskeleton in mesenchymal-to-amoeboid transition of cancer cells.International review of cell and molecular biology · 2020
    Review
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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 3 institutions in 2 countries.

Yvonne BeckhamInstitute for Biophysical Dynamics, University of Chicago Medical Center, Chicago, Illinois, United States of America.
Robert J VasquezSection of Hematology, Oncology and Stem Cell Transplantation, Department of Pediatrics, University of Chicago Medical Center, Chicago, Illinois, United States of America.
Jonathan StrickerJames Franck Institute, University of Chicago, Chicago, Illinois, United States of America; Department of Physics, University of Chicago, Chicago, Illinois, United States of America.
Kareem SayeghJames Franck Institute, University of Chicago, Chicago, Illinois, United States of America; Department of Physics, University of Chicago, Chicago, Illinois, United States of America.
Clement CampilloLaboratoire Physico-Chimie, Institut Curie, Centre de Recherche, Paris, France; Laboratoire Analyse et Modélisation pour la Biologie et l' Environnement, Université d'Evry Val d'Essonne, Evry, France.
Margaret L GardelInstitute for Biophysical Dynamics, University of Chicago Medical Center, Chicago, Illinois, United States of America; James Franck Institute, University of Chicago, Chicago, Illinois, United States of America; Department of Physics, University of Chicago, Chicago, Illinois, United States of America.
University of Chicago · USUniversity of Chicago Medical Center · USInstitut Curie · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Here we demonstrate that Arp2/3 regulates a transition between mesenchymal and amoeboid protrusions in MCF10A epithelial cells. Using genetic and pharmacological means, we first show Arp2/3 inhibition impairs directed cell migration. Arp2/3 inhibition results in a dramatically impaired cell adhesion, causing deficient cell attachment and spreading to ECM as well as an 8-fold decrease in nascent adhesion assembly at the leading edge. While Arp2/3 does not play a significant role in myosin-dependent adhesion growth, mature focal adhesions undergo large scale movements against the ECM suggesting reduced coupling to the ECM. Cell edge protrusions occur at similar rates when Arp2/3 is inhibited but their morphology is dramatically altered. Persistent lamellipodia are abrogated and we observe a markedly increased incidence of blebbing and unstable pseuodopods. Micropipette-aspiration assays indicate that Arp2/3-inhibited cells have a weak coupling between the cell cortex and the plasma membrane, and suggest a potential mechanism for increased pseudopod and bleb formation. Pseudopods are not sensitive to reduced in formin or myosin II activity. Collectively, these results indicate that Arp2/3 is not necessary for rapid protrusion of the cell edge but plays a crucial role in assembling focal adhesions required for its stabilization.

Indexed as

Actin-Related Protein 2-3 ComplexActinsCell Line, TumorCell MembraneCell MovementCell Surface ExtensionsCytoskeletonEpithelial CellsExtracellular MatrixFocal AdhesionsHumansMyosin Type IIOrganoselenium CompoundsOrganosilicon CompoundsRNA InterferenceRNA, Small InterferingActin-Related Protein 2-3 ComplexActinsCK-869Myosin Type IIOrganoselenium CompoundsOrganosilicon CompoundsRNA, Small Interfering

Identifiers

PMID24967897
PMCPMC4072770
OpenAlexW2088875426

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.