Evidence map›Paper›PMID 25225982›Full record

ArticlePloS one2014

Actinomyosin contraction, phosphorylation of VE-cadherin, and actin remodeling enable melanoma-induced endothelial cell-cell junction disassembly.

Eric Weidert, Steven E Pohler, Esther W Gomez, Cheng Dong

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 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Octreotide Counteracts IFN-γ-Induced Endothelial Inflammation.Journal of biochemical and molecular toxicology · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
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

4 authors at 1 institution in 1 country.

Eric WeidertDepartment of Biomedical Engineering, The Pennsylvania State University, University Park, Pennsylvania, United States of America.
Steven E PohlerDepartment of Chemical Engineering, The Pennsylvania State University, University Park, Pennsylvania, United States of America.
Esther W GomezDepartment of Biomedical Engineering, The Pennsylvania State University, University Park, Pennsylvania, United States of America; Department of Chemical Engineering, The Pennsylvania State University, University Park, Pennsylvania, United States of America.
Cheng DongDepartment of Biomedical Engineering, The Pennsylvania State University, University Park, Pennsylvania, United States of America.
Pennsylvania State University · US

Funding

Multiscale modeling of leukocyte-tumor cell adhesion to endothelium in shear flowR01CA125707 · NCI · PENNSYLVANIA STATE UNIVERSITY, THE · PI DONG, CHENG · 2007 to 2010
$933k
NCI NIH HHS CA-125707NCI NIH HHS R01 CA125707
6 · The paper itself

Abstract

During melanoma cell extravasation through the vascular endothelium, melanoma cells interact with endothelial cells through secretion of cytokines and by adhesion between proteins displayed on opposing cell surfaces. How these tumor cell associated signals together regulate the dynamics of intracellular signaling pathways within endothelial cells leading to endothelial cell-cell junction disruption is not well understood. Here, we used a combination of experimental and computational approaches to examine the individual and combined effects of activation of the vascular cell adhesion molecule (VCAM)-1, interleukin (IL)-8, and IL-1β signaling pathways on the integrity of vascular junctions. Our simulations predict a multifaceted interplay of signaling resulting from individual activation of VCAM-1, IL-8 and IL-1β pathways that is neither synergistic nor additive compared to all inputs turned on simultaneously. Furthermore, we show that the levels of phosphorylated proteins associated with actinomyosin contractility and junction disassembly peak prior to those related to actin remodeling. The results of this work provide insight into the dynamics of tumor-mediated endothelial junction disassembly and suggest that targeting proteins downstream of several interaction pathways may be the most effective therapeutic approach to reduce melanoma extravasation.

Indexed as

ActinsAntigens, CDCadherin 5CadherinsCell Line, TumorCoculture TechniquesCytoskeletonEndothelial CellsGene Knockout TechniquesHumansHuman Umbilical Vein Endothelial CellsIntercellular JunctionsInterleukin-1betaInterleukin-8MelanomaModels, BiologicalActinsAntigens, CDCadherin 5CadherinsInterleukin-1betaInterleukin-8Myosin-Light-Chain KinaseVascular Cell Adhesion Molecule-1

Identifiers

PMID25225982
PMCPMC4167543
OpenAlexW2071395071

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.