Evidence map›Paper›PMID 23511848›Full record

ArticleSmall GTPases

RhoA goes GLOBAL.

Caitlin Collins, Ellie Tzima

Abstract readComment
In one paragraph

Article in Small GTPases. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Biophysical Tools to Study Cellular Mechanotransduction.Bioengineering (Basel, Switzerland) · 2017
    Review
  2. Endothelial Mechanosignaling: Does One Sensor Fit All?Antioxidants & redox signaling · 2016
    Review
  3. Flow shear stress differentially regulates endothelial uptake of nanocarriers targeted to distinct epitopes of PECAM-1.Journal of controlled release : official journal of the Controlled Release Society · 2015
    Article
  4. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Caitlin CollinsDepartment of Cell Biology and Physiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Ellie Tzima

Funding

Endothelial cell junctions in mechanotransductionR01HL088632 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI TZIMA, ELLIE · 2008 to 2012
$2.1M
NHLBI NIH HHS HL088632NHLBI NIH HHS R01 HL088632
6 · The paper itself

Abstract

Mechanical forces influence nearly all aspects of biology. Cells are equipped with numerous mechanosensitive proteins that activate various signaling cascades in response to mechanical cues from their environment. Much interest lies in understanding how cells respond to external stresses. A number of studies have highlighted the coordination of mechanical and chemical signaling cascades downstream of integrins. In recent years, the study of mechanotransduction has expanded to other mechanosensitive adhesion receptors, such as platelet endothelial cell adhesion molecule-1 (PECAM-1). This commentary will highlight our current understanding of integrin and PECAM-1-mediated mechanotransduction and expand on the observation that a localized mechanical stress can elicit a global mechanosignaling response.

Indexed as

AnimalsEndothelial CellsIntegrinsMechanotransduction, CellularPlatelet Endothelial Cell Adhesion Molecule-1rhoA GTP-Binding ProteinIntegrinsPlatelet Endothelial Cell Adhesion Molecule-1rhoA GTP-Binding Proteincytoskeletonfocal adhesionforceintegrinmechanotransductionPECAM-1RhoA

Identifiers

PMID23511848
PMCPMC3747253

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.