Evidence map›Paper›PMID 22649559›Full record

ArticlePloS one2012

Rgnef (p190RhoGEF) knockout inhibits RhoA activity, focal adhesion establishment, and cell motility downstream of integrins.

Nichol L G Miller, Christine Lawson, Xiao Lei Chen, Ssang-Taek Lim, David D Schlaepfer

Abstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–field-weighted citation impact
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

25 citing papers in PubMed.

  1. Intracellular protein GBF1 displays significant associations with amyloid pathology in Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Article
  2. Article
  3. Functions of RhoA in the female reproductive system.Reproductive and developmental medicine · 2025
    Review
  4. Review
  5. Guanine nucleotide exchange factors and colon neoplasia.Frontiers in cell and developmental biology · 2024
    Review
  6. The Role of NQO1 in Ovarian Cancer.International journal of molecular sciences · 2023
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. 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

5 authors.

Nichol L G MillerMoores Cancer Center, University of California San Diego, La Jolla, California, United States of America.
Christine Lawson
Xiao Lei Chen
Ssang-Taek Lim
David D Schlaepfer

Funding

Genetic Analysis of FAK ActivityR01GM087400 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SCHLAEPFER, DAVID D · 2009 to 2012
$1.2M
Role of p190RhoGEF (Rgnef) in cell motility and tumor progressionF32CA159558 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI MILLER, NICHOL L G · 2011 to 2013
$154k
CIHR 200810MFE-193594-139144NCI NIH HHS 1F32CA159558NCI NIH HHS F32 CA159558NIGMS NIH HHS GM087400NIGMS NIH HHS R01 GM087400
6 · The paper itself

Abstract

backgroundCell migration is a highly regulated process that involves the formation and turnover of cell-matrix contact sites termed focal adhesions. Rho-family GTPases are molecular switches that regulate actin and focal adhesion dynamics in cells. Guanine nucleotide exchange factors (GEFs) activate Rho-family GTPases. Rgnef (p190RhoGEF) is a ubiquitous 190 kDa GEF implicated in the control of colon carcinoma and fibroblast cell motility. PRINCIPAL

findingsRgnef exon 24 floxed mice (Rgnef(flox)) were created and crossed with cytomegalovirus (CMV)-driven Cre recombinase transgenic mice to inactivate Rgnef expression in all tissues during early development. Heterozygous Rgnef(WT/flox) (Cre+) crosses yielded normal Mendelian ratios at embryonic day 13.5, but Rgnef(flox/flox) (Cre+) mice numbers at 3 weeks of age were significantly less than expected. Rgnef(flox/flox) (Cre+) (Rgnef-/-) embryos and primary mouse embryo fibroblasts (MEFs) were isolated and verified to lack Rgnef protein expression. When compared to wildtype (WT) littermate MEFs, loss of Rgnef significantly inhibited haptotaxis migration, wound closure motility, focal adhesion number, and RhoA GTPase activation after fibronectin-integrin stimulation. In WT MEFs, Rgnef activation occurs within 60 minutes upon fibronectin plating of cells associated with RhoA activation. Rgnef-/- MEF phenotypes were rescued by epitope-tagged Rgnef re-expression.

conclusionsRgnef-/- MEF phenotypes were due to Rgnef loss and support an essential role for Rgnef in RhoA regulation downstream of integrins in control of cell migration.

Indexed as

Analysis of VarianceAnimalsCell MovementDNA PrimersEmbryo, MammalianFibroblastsFibronectinsFluorescent Antibody TechniqueFocal AdhesionsGenotypeGuanine Nucleotide Exchange FactorsImmunohistochemistryIntegrinsMiceMice, Knockoutras-GRF1DNA PrimersFibronectinsGuanine Nucleotide Exchange FactorsIntegrinsras-GRF1Rasgrf1 protein, mouserhoA GTP-Binding Protein

Identifiers

PMID22649559
PMCPMC3359313

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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.