Evidence map›Paper›PMID 12196635›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2002

The antiangiogenic activity of cleaved high molecular weight kininogen is mediated through binding to endothelial cell tropomyosin.

Jing-Chuan Zhang, Fernando Donate, Xiaoping Qi, Nicholas P Ziats, Jose C Juarez, Andrew P Mazar, Yuan-Ping Pang, Keith R McCrae

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

19 citing papers in PubMed, 54 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Cell death pathways and viruses: Role of microRNAs.Molecular therapy. Nucleic acids · 2021
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Regulatory effects of ferritin on angiogenesis.Proceedings of the National Academy of Sciences of the United States of America · 2009
    Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Antiangiogenic gene therapy of cancer: recent developments.Journal of translational medicine · 2004
    Article
  19. Angiogenesis inhibitors found within the haemostasis pathway.Journal of cellular and molecular medicine
    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

8 authors at 3 institutions in 1 country.

Jing-Chuan ZhangDivision of Hematology-Oncology, Case Western Reserve University School of Medicine and University Hospitals of Cleveland, Cleveland, OH 44106, USA.
Fernando Donate
Xiaoping Qi
Nicholas P Ziats
Jose C Juarez
Andrew P Mazar
Yuan-Ping Pang
Keith R McCrae
Case Western Reserve University · USMayo Clinic · USUniversity Hospitals of Cleveland · US

Funding

ANTI ANGIOGENIC ACTIVITY OF CLEAVED HMW KININOGENR01CA083134 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI MCCRAE, KEITH R. · 2000 to 2004
$2.0M
NCI NIH HHS R01 CA083134NCI NIH HHS R01 CA83134
6 · The paper itself

Abstract

Conformationally altered proteins and protein fragments derived from the extracellular matrix and hemostatic system may function as naturally occurring angiogenesis inhibitors. One example of such a protein is cleaved high molecular weight kininogen (HKa). HKa inhibits angiogenesis by inducing apoptosis of proliferating endothelial cells, effects mediated largely by HKa domain 5. However, the mechanisms underlying the antiangiogenic activity of HKa have not been characterized, and its binding site on proliferating endothelial cells has not been defined. Here, we report that the induction of endothelial cell apoptosis by HKa, as well as the antiangiogenic activity of HKa in the chick chorioallantoic membrane, was inhibited completely by antitropomyosin monoclonal antibody TM-311. TM-311 also blocked the high-affinity Zn2+-dependent binding of HKa to both purified tropomyosin and proliferating endothelial cells. Confocal microscopic analysis of endothelial cells stained with monoclonal antibody TM-311, as well as biotin labeling of cell surface proteins on intact endothelial cells, revealed that tropomyosin exposure was enhanced on the surface of proliferating cells. These studies demonstrate that the antiangiogenic effects of HKa depend on high-affinity binding to endothelial cell tropomyosin.

Indexed as

AllantoisAngiogenesis InhibitorsAnimalsAntibodies, MonoclonalApoptosisBase SequenceCells, CulturedChick EmbryoChorionDNA, ComplementaryEndothelium, VascularHumansKininogen, High-Molecular-WeightNeovascularization, PhysiologicProtein BindingRecombinant ProteinsAngiogenesis InhibitorsAntibodies, MonoclonalDNA, ComplementaryKininogen, High-Molecular-WeightRecombinant ProteinsTropomyosin

Identifiers

PMID12196635
PMCPMC129426
OpenAlexW2059666020

What OpenQuestion holds

Textmetadata
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.