Evidence map›Paper›PMID 28035064›Full record

ArticleOncotarget2017

Functional assessment of von Willebrand factor expression by cancer cells of non-endothelial origin.

Anahita Mojiri, Konstantin Stoletov, Maria Areli Lorenzana Carrillo, Lian Willetts, Saket Jain, Roseline Godbout, Paul Jurasz, Consolato M Sergi, David D Eisenstat, John D Lewis and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. 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
3.1field-weighted citation impact, top 8% 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

25 citing papers in PubMed, 54 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Von Willebrand factor and hematogenous cancer metastasis under flow.Frontiers in cell and developmental biology · 2024
    Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Mechanisms and biomarkers of cancer-associated thrombosis.Translational research : the journal of laboratory and clinical medicine · 2020
    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

11 authors at 1 institution in 1 country.

Anahita MojiriDepartment of Medicine, University of Alberta, Edmonton, Alberta, Canada.
Konstantin StoletovDepartment of Oncology, University of Alberta, Edmonton, Alberta, Canada.
Maria Areli Lorenzana CarrilloDepartment of Medicine, University of Alberta, Edmonton, Alberta, Canada.
Lian WillettsDepartment of Oncology, University of Alberta, Edmonton, Alberta, Canada.
Saket JainDepartment of Oncology, University of Alberta, Edmonton, Alberta, Canada.
Roseline GodboutDepartment of Oncology, University of Alberta, Edmonton, Alberta, Canada.
Paul JuraszDepartment of Pharmacy and Pharmaceutical Sciences, University of Alberta, Edmonton, Alberta, Canada.
Consolato M SergiDepartment of Laboratory Medicine and Pathology, University of Alberta, Edmonton, Alberta, Canada.
David D EisenstatDepartment of Oncology, University of Alberta, Edmonton, Alberta, Canada.
John D LewisDepartment of Oncology, University of Alberta, Edmonton, Alberta, Canada.
Nadia JahroudiDepartment of Medicine, University of Alberta, Edmonton, Alberta, Canada.
University of Alberta · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Von Willebrand factor (VWF) is a highly adhesive procoagulant molecule that mediates platelet adhesion to endothelial and subendothelial surfaces. Normally it is expressed exclusively in endothelial cells (ECs) and megakaryocytes. However, a few studies have reported VWF detection in cancer cells of non-endothelial origin, including osteosarcoma. A role for VWF in cancer metastasis has long been postulated but evidence supporting both pro- and anti-metastatic roles for VWF has been presented. We hypothesized that the role of VWF in cancer metastasis is influenced by its cellular origin and that cancer cell acquisition of VWF expression may contribute to enhanced metastatic potential. We demonstrated de novo expression of VWF in glioma as well as osteosarcoma cells. Endothelial monolayer adhesion, transmigration and extravasation capacities of VWF expressing cancer cells were shown to be enhanced compared to non-VWF expressing cells, and were significantly reduced as a result of VWF knock down. VWF expressing cancer cells were also detected in patient tumor samples of varying histologies. Analyses of the mechanism of transcriptional activation of the VWF in cancer cells demonstrated a pattern of trans-activating factor binding and epigenetic modifications consistent overall with that observed in ECs. These results demonstrate that cancer cells of non-endothelial origin can acquire de novo expression of VWF, which can enhance processes, including endothelial and platelet adhesion and extravasation, that contribute to cancer metastasis.

Indexed as

AnimalsChick EmbryoChromatin ImmunoprecipitationDNA MethylationFluorescent Antibody TechniqueGene Knockdown TechniquesGliomaHumansImmunohistochemistryMiceNeoplasm InvasivenessNeoplasmsOsteosarcomavon Willebrand Factorvon Willebrand Factorcancerextravasationtranscriptiontranscription factorvon Willebrand factor

Identifiers

PMID28035064
PMCPMC5355073
OpenAlexW2564283772

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.