Evidence map›Paper›PMID 21685891›Full record

ArticleNature cell biology2011

RasGRF suppresses Cdc42-mediated tumour cell movement, cytoskeletal dynamics and transformation.

Fernando Calvo, Victoria Sanz-Moreno, Lorena Agudo-Ibáñez, Fredrik Wallberg, Erik Sahai, Christopher J Marshall, Piero Crespo

Erratum issuedAbstract readVideo-Audio Media
PubMed Publisher
In one paragraph

Article in Nature cell biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

51 citing papers in PubMed, 80 citations in OpenAlex.

  1. Article
  2. Article
  3. Pan-cancer drivers of metastasis.Molecular cancer · 2025
    Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Molecular subversion of Cdc42 signalling in cancer.Biochemical Society transactions · 2021
    Review
  9. Article
  10. Article
  11. Article
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  13. Article
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4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

7 authors at 4 institutions in 2 countries.

Fernando CalvoInstituto de Biomedicina y Biotecnología de Cantabria (IBBTEC), Consejo Superior de Investigaciones Científicas-IDICAN-Universidad de Cantabria, Departamento de Biología Molecular, Facultad de Medicina, Santander, 39011, Cantabria, Spain.
Victoria Sanz-Moreno
Lorena Agudo-Ibáñez
Fredrik Wallberg
Erik Sahai
Christopher J Marshall
Piero Crespo
Universidad de Cantabria · ESCancer Research UK · GBInstitute of Cancer Research · GBKing's College London · GB

Funding

Cancer Research UK 12065
6 · The paper itself

Abstract

Individual tumour cells move in three-dimensional environments with either a rounded or an elongated 'mesenchymal' morphology. These two modes of movement are tightly regulated by Rho family GTPases: elongated movement requires activation of Rac1, whereas rounded/amoeboid movement engages specific Cdc42 and Rho signalling pathways. In siRNA screens targeting the genes encoding guanine nucleotide exchange factors (GEFs), we found that the Ras GEF RasGRF2 regulates conversion between elongated- and rounded-type movement. RasGRF2 suppresses rounded movement by inhibiting the activation of Cdc42 independently of its capacity to activate Ras. RasGRF2 and RasGRF1 directly bind to Cdc42, outcompeting Cdc42 GEFs, thereby preventing Cdc42 activation. By this mechanism, RasGRFs regulate other Cdc42-mediated cellular processes such as the formation of actin spikes, transformation and invasion in vitro and in vivo. These results demonstrate a role for RasGRF GEFs as negative regulators of Cdc42 activation.

Indexed as

Cell MovementCell ShapeAnimalscdc42 GTP-Binding ProteinCell Transformation, NeoplasticChlorocebus aethiopsCOS CellsCytoskeletonDown-RegulationEnzyme ActivationHeLa CellsHumansJurkat CellsMelanomaMiceMicroscopy, Videocdc42 GTP-Binding ProteinProto-Oncogene Proteins c-vavras-GRF1RASGRF1 protein, humanRasgrf1 protein, mouseRASGRF2 protein, humanRasgrf2 protein, mouseras Guanine Nucleotide Exchange FactorsRecombinant Fusion Proteins

Identifiers

PMID21685891
OpenAlexW1986074141

What OpenQuestion holds

Textmetadata
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.