Evidence map›Paper›PMID 21196249›Full record

ReviewFrontiers in bioscience (Landmark edition)2011

Targeting the anthrax receptors, TEM-8 and CMG-2, for anti-angiogenic therapy.

Lorna M Cryan, Michael S Rogers

Open access · bronzeAbstract readReview
In one paragraph

Review in Frontiers in bioscience (Landmark edition), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
1.5field-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

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 47 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
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  5. Article
  6. Review
  7. AB Toxins as High-Affinity Ligands for Cell Targeting in Cancer Therapy.International journal of molecular sciences · 2023
    Review
  8. Article
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  15. Solid tumor therapy by selectively targeting stromal endothelial cells.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
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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

2 authors at 1 institution in 1 country.

Lorna M CryanDepartment of Surgery, Children's Hospital Boston, Boston, MA 02115, USA.
Michael S Rogers
Boston Children's Hospital · US

Funding

Novel Angiogenesis Inhibitors Targeting the Anthrax Toxin ReceptorsR01EY018829 · NEI · BOSTON CHILDREN'S HOSPITAL · PI ROGERS, MICHAEL SEAN · 2008 to 2012
$2.0M
NEI NIH HHS R01 EY018829
6 · The paper itself

Abstract

The anthrax toxin receptors tumor endothelial marker-8 (TEM-8) and capillary morphogenesis gene-2 (CMG-2) are responsible for allowing entry of anthrax toxin into host cells. These receptors were first discovered due to their enhanced expression on endothelial cells undergoing blood vessel growth or angiogenesis in model systems. Inhibition of angiogenesis is an important strategy for current anti-cancer therapies and treatment of retinal diseases. Functional roles for TEM-8 and CMG-2 in angiogenesis have recently emerged. TEM-8 appears to regulate endothelial cell migration and tubule formation whereas a role for CMG-2 in endothelial proliferation has been documented. TEM-8 and CMG-2 bind differentially to extracellular matrix proteins including collagen I, collagen IV and laminin and these properties may be responsible for their apparent roles in regulating endothelial cell behavior during angiogenesis. TEM-8-binding moieties have also been suggested to be useful in selectively targeting anti-angiogenic and anti-tumorigenic therapies to tumor endothelium. Additionally, studies of modified forms of lethal toxin (LeTx) have demonstrated that targeted inhibition of MAPKs within tumor vessels may represent an efficacious anti-angiogenic strategy.

Indexed as

Angiogenesis InhibitorsAnimalsAntigens, BacterialAntineoplastic AgentsBacterial ToxinsEndothelial CellsExtracellular MatrixHumansMembrane ProteinsMicrofilament ProteinsNeoplasm ProteinsNeovascularization, PathologicReceptors, Cell SurfaceReceptors, PeptideAngiogenesis Inhibitorsanthrax toxinAntigens, BacterialAntineoplastic AgentsANTXR1 protein, humanANTXR2 protein, humanBacterial ToxinsMembrane ProteinsMicrofilament ProteinsNeoplasm ProteinsReceptors, Cell SurfaceReceptors, Peptide

Identifiers

PMID21196249
PMCPMC3066103
OpenAlexW960284382

What OpenQuestion holds

Textmetadata
LicenceTDM
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.