Evidence map›Paper›PMID 24519883›Full record

ArticleCancer medicine2014

Cryptic collagen IV promotes cell migration and adhesion in myeloid leukemia.

Amanda J Favreau, Calvin P H Vary, Peter C Brooks, Pradeep Sathyanarayana

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 15% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. The Duality of Collagens in Metastases of Solid Tumors.International journal of molecular sciences · 2025
    Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Leukaemia: a model metastatic disease.Nature reviews. Cancer · 2021
    Review
  10. Article
  11. Article
  12. The role of collagen in cancer: from bench to bedside.Journal of translational medicine · 2019
    Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  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

4 authors at 3 institutions in 1 country.

Amanda J FavreauCenter for Molecular Medicine, Maine Medical Center Research Institute, Scarborough, 04074, Maine; The Graduate School of Biomedical Science and Engineering, University of Maine, Orono, 04469, Maine.
Calvin P H Vary
Peter C Brooks
Pradeep Sathyanarayana
Maine Medical Center Research Institute · USTufts University · USUniversity of Maine · US

Funding

Progenitor Cell Analysis CoreP30GM106391 · NIGMS · MAINEHEALTH · PI WOJCHOWSKI, DON MICHAEL · 2013 to 2017
$5.7M
Phase III COBRE in Vascular BiologyP30GM103392 · NIGMS · MAINEHEALTH · PI ST. GERMAIN, DONALD L. · 2012 to 2016
$4.7M
CRYPTIC DOMAINS OF COLLAGEN IV IN TUMOR GROWTHR01CA091645 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BROOKS, PETER C. · 2000 to 2011
$3.3M
COBRE in Stem Cell Biology and Regenerative MedicineP20GM103465 · NIGMS · MAINEHEALTH · PI WOJCHOWSKI, DON MICHAEL · 2012 to 2012
$2.0M
PHASE III COBRE IN VASCULAR BIOLOGYP30RR030927 · NCRR · MAINEHEALTH · PI FRIESEL, ROBERT E · 2011 to 2011
$1.2M
NCI NIH HHS CA91645/NCINCRR NIH HHS P30 RR030927NIGMS NIH HHS 8P20GM103465NIGMS NIH HHS P20 GM103465NIGMS NIH HHS P30 GM103392NIGMS NIH HHS P30 GM106391PHS HHS HL083151/NHLBIPHS HHS NIH/NIGMS 8P20GM103465PHS HHS NIH/NIGMS P30GM103392
6 · The paper itself

Abstract

Previously, we showed that discoidin domain receptor 1 (DDR1), a class of collagen-activated receptor tyrosine kinase (RTK) was highly upregulated on bone marrow (BM)-derived CD33+ leukemic blasts of acute myeloid leukemia (AML) patients. Herein as DDR1 is a class of collagen-activated RTK, we attempt to understand the role of native and remodeled collagen IV in BM microenvironment and its functional significance in leukemic cells. Exposure to denatured collagen IV significantly increased the migration and adhesion of K562 cells, which also resulted in increased activation of DDR1 and AKT. Further, levels of MMP9 were increased in conditioned media (CM) of denatured collagen IV exposed cells. Mass spectrometric liquid chromatography/tandem mass spectrometry QSTAR proteomic analysis revealed exclusive presence of Secretogranin 3 and InaD-like protein in the denatured collagen IV CM. Importantly, BM samples of AML patients exhibited increased levels of remodeled collagen IV compared to native as analyzed via anti-HUIV26 antibody. Taken together, for the first time, we demonstrate that remodeled collagen IV is a potent activator of DDR1 and AKT that also modulates both migration and adhesion of myeloid leukemia cells. Additionally, high levels of the HUIV26 cryptic collagen IV epitope are expressed in BM of AML patients. Further understanding of this phenomenon may lead to the development of therapeutic agents that directly modulate the BM microenvironment and attenuate leukemogenesis.

Indexed as

Cell AdhesionCell MovementCollagen Type IVHumansK562 CellsLeukemia, MyeloidTransfectionTumor Cells, CulturedCollagen Type IVAKTAMLcollagenDDR1microenvironment

Identifiers

PMID24519883
PMCPMC3987076
OpenAlexW2028936731

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.