Evidence map›Paper›PMID 32705984›Full record

ArticleeLife2020

Periodic propagating waves coordinate RhoGTPase network dynamics at the leading and trailing edges during cell migration.

Alfonso Bolado-Carrancio, Oleksii S Rukhlenko, Elena Nikonova, Mikhail A Tsyganov, Anne Wheeler, Amaya Garcia-Munoz, Walter Kolch, Alex von Kriegsheim, Boris N Kholodenko

Open access · goldAbstract read
In one paragraph

Article in eLife, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
4.4field-weighted citation impact, top 4% 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

38 citing papers in PubMed, 59 citations in OpenAlex.

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  10. Substrate stress relaxation regulates neural stem cell fate commitment.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  11. Article
  12. Patterning of the cell cortex by Rho GTPases.Nature reviews. Molecular cell biology · 2024
    Review
  13. Mesenchymal cell migration on one-dimensional micropatterns.Frontiers in cell and developmental biology · 2024
    Review
  14. Article
  15. Article
  16. Competition and Synergy of Arp2/3 and Formins in Nucleating Actin Waves.bioRxiv : the preprint server for biology · 2023
    Article
  17. Article
  18. Article
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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 2 institutions in 4 countries.

Alfonso Bolado-Carrancio *Edinburgh Cancer Research Centre, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, United Kingdom.
Oleksii S Rukhlenko *Systems Biology Ireland, School of Medicine and Medical Science, University College Dublin, Belfield, Ireland.ORCID 0000-0003-1863-4987
Elena NikonovaSystems Biology Ireland, School of Medicine and Medical Science, University College Dublin, Belfield, Ireland.
Mikhail A TsyganovSystems Biology Ireland, School of Medicine and Medical Science, University College Dublin, Belfield, Ireland.
Anne WheelerEdinburgh Cancer Research Centre, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, United Kingdom.
Amaya Garcia-MunozSystems Biology Ireland, School of Medicine and Medical Science, University College Dublin, Belfield, Ireland.
Walter KolchSystems Biology Ireland, School of Medicine and Medical Science, University College Dublin, Belfield, Ireland.
Alex von KriegsheimEdinburgh Cancer Research Centre, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, United Kingdom.ORCID 0000-0002-4952-8573
Boris N KholodenkoSystems Biology Ireland, School of Medicine and Medical Science, University College Dublin, Belfield, Ireland.ORCID 0000-0002-9483-4975
University College Dublin · IEEdinburgh Cancer Research · GB

Funding

Multiscale Modeling to Optimize Inhibition of Oncogenic ERK Pathway SignalingR01CA244660 · NCI · YALE UNIVERSITY · PI HLAVACEK, WILLIAM S, KHOLODENKO, BORIS N · 2020 to 2024
$3.4M
Breast Cancer Now PR183Cancer Research UK C157/A25140Horizon 2020 Framework Programme 686098Horizon 2020 Framework Programme 731032NCI NIH HHS R01 CA244660Science Foundation Ireland 14/IA/2395Science Foundation Ireland 18/SPP/3522
6 · The paper itself

Abstract

Migrating cells need to coordinate distinct leading and trailing edge dynamics but the underlying mechanisms are unclear. Here, we combine experiments and mathematical modeling to elaborate the minimal autonomous biochemical machinery necessary and sufficient for this dynamic coordination and cell movement. RhoA activates Rac1 via DIA and inhibits Rac1 via ROCK, while Rac1 inhibits RhoA through PAK. Our data suggest that in motile, polarized cells, RhoA-ROCK interactions prevail at the rear, whereas RhoA-DIA interactions dominate at the front where Rac1/Rho oscillations drive protrusions and retractions. At the rear, high RhoA and low Rac1 activities are maintained until a wave of oscillatory GTPase activities from the cell front reaches the rear, inducing transient GTPase oscillations and RhoA activity spikes. After the rear retracts, the initial GTPase pattern resumes. Our findings show how periodic, propagating GTPase waves coordinate distinct GTPase patterns at the leading and trailing edge dynamics in moving cells.

Indexed as

Cell MovementCell PolarityCell Line, TumorHumansrac1 GTP-Binding ProteinrhoA GTP-Binding Proteinrho-Associated Kinasesrac1 GTP-Binding ProteinRAC1 protein, humanrhoA GTP-Binding ProteinRHOA protein, humanrho-Associated KinasesROCK1 protein, humancell biologycell migrationcomputational biologyhumanmathematical modelingnonlinear dynamicsoscillations and wavesrho gtpasessystems biology

Identifiers

PMID32705984
PMCPMC7380942
OpenAlexW3044725762

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.