Evidence map›Paper›PMID 24194929›Full record

ArticlePloS one2013

Proteolysis during tumor cell extravasation in vitro: metalloproteinase involvement across tumor cell types.

Evelyn B Voura, Jane L English, Hoi-Ying E Yu, Andrew T Ho, Patrick Subarsky, Richard P Hill, Carlo V Hojilla, Rama Khokha

Abstract read
In one paragraph

Article in PloS one, 2013. 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. Review
  2. Mechanobiology in oncology: basic concepts and clinical prospects.Frontiers in cell and developmental biology · 2023
    Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Metastasis prevention: targeting causes and roots.Clinical & experimental metastasis · 2022
    Review
  8. Review
  9. Metastasis and MAPK Pathways.International journal of molecular sciences · 2022
    Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. The Role of Mesenchymal Stem Cells in Radiation-Induced Lung Fibrosis.International journal of molecular sciences · 2019
    Review
  16. The Expanding Role of MT1-MMP in Cancer Progression.Pharmaceuticals (Basel, Switzerland) · 2019
    Review
  17. Review
  18. Review
  19. Article
  20. 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

8 authors.

Evelyn B VouraOntario Cancer Institute, Princess Margaret Hospital, Toronto, Ontario, Canada ; Department of Biology, Dominican College, Orangeburg, New York, United States of America.
Jane L English
Hoi-Ying E Yu
Andrew T Ho
Patrick Subarsky
Richard P Hill
Carlo V Hojilla
Rama Khokha

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To test if proteolysis is involved in tumor cell extravasation, we developed an in vitro model where tumor cells cross an endothelial monolayer cultured on a basement membrane. Using this model we classified the ability of the cells to transmigrate through the endothelial cell barrier onto the underlying matrix, and scored this invasion according to the stage of passage through the endothelium. Metalloproteinase inhibitors reduced tumor cell extravasation by at least 35%. Visualization of protease and cell adhesion molecules by confocal microscopy demonstrated the cell surface localization of MMP-2, MMP-9, MT1-MMP, furin, CD44 and αvβ3, during the process of transendothelial migration. By the addition of inhibitors and bio-modulators we assessed the functional requirement of the aforementioned molecules for efficient migration. Proteolytic digestion occurred at the cell-matrix interface and was most evident during the migratory stage. All of the inhibitors and biomodulators affected the transition of the tumor cells into the migratory stage, highlighting the most prevalent use of proteolysis at this particular step of tumor cell extravasation. These data suggest that a proteolytic interface operates at the tumor cell surface within the tumor-endothelial cell microenvironment.

Indexed as

ProteolysisBlotting, WesternCell Adhesion MoleculesFluorescent Antibody TechniqueHumansIn Vitro TechniquesMetalloproteasesMicroscopy, ConfocalTransendothelial and Transepithelial MigrationTumor Cells, CulturedTumor MicroenvironmentCell Adhesion MoleculesMetalloproteases

Identifiers

PMID24194929
PMCPMC3806793

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.