Evidence map›Paper›PMID 29222169›Full record

ArticleMolecular cancer research : MCR2018

Nanoscale Tuning of VCAM-1 Determines VLA-4-Dependent Melanoma Cell Plasticity on RGD Motifs.

Katharina Amschler, Eugen Kossmann, Luise Erpenbeck, Sebastian Kruss, Tillmann Schill, Margarete Schön, Sigrid M C Möckel, Joachim P Spatz, Michael P Schön

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cancer research : MCR, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

9 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. The Cancer Microenvironment: Mechanical Challenges of the Metastatic Cascade.Frontiers in bioengineering and biotechnology · 2021
    Review
  5. Article
  6. Article
  7. Review
  8. Extracellular Matrix Alterations in Metastatic Processes.International journal of molecular sciences · 2019
    Review
  9. Article
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 1 country.

Katharina Amschler *Department of Dermatology, Venereology and Allergology, University Medical Center, Göttingen, Germany.
Eugen Kossmann *Department of Dermatology, Venereology and Allergology, University Medical Center, Göttingen, Germany.
Luise ErpenbeckDepartment of Dermatology, Venereology and Allergology, University Medical Center, Göttingen, Germany.
Sebastian KrussDepartment of Physical Chemistry, Georg August University, Göttingen, Germany.
Tillmann SchillDepartment of Dermatology, Venereology and Allergology, University Medical Center, Göttingen, Germany.
Margarete SchönDepartment of Dermatology, Venereology and Allergology, University Medical Center, Göttingen, Germany.
Sigrid M C MöckelDepartment of Dermatology, Venereology and Allergology, University Medical Center, Göttingen, Germany.
Joachim P SpatzDepartment of Cellular Biophysics, Max Planck Institute for Medical Research, Heidelberg and Laboratory of Biophysical Chemistry, University of Heidelberg, Heidelberg, Germany.
Michael P SchönDepartment of Dermatology, Venereology and Allergology, University Medical Center, Göttingen, Germany. Michael.schoen@med.uni-goettingen.de.
University of Göttingen · DEHeidelberg University · DE

Funding

European Research Council 294852
6 · The paper itself

Abstract

The biophysical fine-tuning of cancer cell plasticity is crucial for tumor progression but remains largely enigmatic. Although vascular cell adhesion molecule-1 (VCAM-1/CD106) has been implicated in melanoma progression, here its presentation on endothelial cells was associated with diminished melanoma cell spreading. Using a specific nanoscale modulation of VCAM-1 (tunable from 70 to 670 ligands/μm²) next to integrin ligands (RGD motifs) in a bifunctional system, reciprocal regulation of integrin α4 (ITGA4/VLA-4/CD49d)-dependent adhesion and spreading of melanoma cells was found. As the VCAM-1/VLA-4 receptor pair facilitated adhesion, while at the same time antagonizing RGD-mediated spreading, melanoma cell morphogenesis on these bifunctional matrices was directly regulated by VCAM-1 in a dichotomic and density-dependent fashion. This was accompanied by concordant regulation of F-actin cytoskeleton remodeling, Rac1-expression, and paxillin-related adhesion formation. The novel function of VCAM-1 was corroborated

Indexed as

AnimalsCell AdhesionCell Line, TumorCell PlasticityHumansIntegrin alpha4beta1MaleMelanomaMelanoma, ExperimentalMiceNanotechnologyOligopeptidesTransfectionVascular Cell Adhesion Molecule-1arginyl-glycyl-aspartic acidIntegrin alpha4beta1OligopeptidesVascular Cell Adhesion Molecule-1

Identifiers

PMID29222169
PMCPMC5837006
OpenAlexW2772464863

What OpenQuestion holds

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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.