Evidence map›Paper›PMID 17235351›Full record

ArticleCancer gene therapy2007

Mapping of angiogenic markers for targeting of vectors to tumor vascular endothelial cells.

Y Tang, P Borgstrom, J Maynard, J Koziol, Z Hu, A Garen, A Deisseroth

Abstract read
PubMed Publisher
In one paragraph

Article in Cancer gene therapy, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

20 citing papers in PubMed, 32 citations in OpenAlex.

  1. Tissue Factor-Targeted "OFrontiers in oncology · 2020
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  13. Active adenoviral vascular penetration by targeted formation of heterocellular endothelial-epithelial syncytia.Molecular therapy : the journal of the American Society of Gene Therapy · 2011
    Article
  14. Article
  15. Article
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  17. Article
  18. Article
  19. Article
  20. Tissue factor, angiogenesis and tumour progression.Breast cancer research : BCR · 2008
    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

7 authors at 3 institutions in 1 country.

Y TangSidney Kimmel Cancer Center, San Diego, CA 92121, USA.
P Borgstrom
J Maynard
J Koziol
Z Hu
A Garen
A Deisseroth
Sidney Kimmel Cancer Center · USYale University · USScripps Research Institute · US

Funding

Targeting Vessels in TumorsP01CA104898 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI TALAMINI, MARK A · 2005 to 2009
$13.8M
Tumor Neovasculature Vector TargetingR21CA096232 · NCI · SIDNEY KIMMEL CANCER CENTER · PI DEISSEROTH, ALBERT B · 2002 to 2003
$693k
NCI NIH HHS CA 104898-01NCI NIH HHS R21CA096232-01
6 · The paper itself

Abstract

The vasculature of mouse breast tumor spheroids grown on mammary fat pad tissue in an intravital microscopy (IVM) viewing chamber was shown to derive from infiltrating angiogenic mammary vessels. The receptors tissue factor (TF), alpha V beta 3 integrin and Tie-2 were expressed on the vascular endothelium in the periphery but not in the center of the tumor spheroids nor in the mammary tissue nor in smooth muscle tissue, whereas Tie-1 and PCAM-1 were expressed extensively in the entire tumor and in the vascular endothelium of the entire tumor nodule and in normal mammary tissue. TF is a specific target for adenoviral vector-mediated cancer immunotherapy. Subcutaneous injection of the AdfVII/IgG(1)Fc vector leads to the release into the system circulation of a fVII/IgG(1)Fc immunoconjugate molecule that binds specifically and tightly to TF on vascular endothelial cells and tumor cells, activating a cytolytic immune response against the targeted cells. We show that a single administration of the AdfVII/IgG(1)Fc vector destroys the peripheral but not the central vasculature of a tumor spheroid, causing partial tumor regression; additional administrations prevent regeneration of the peripheral vasculature and regrowth of the tumor. These findings indicate that a critical parameter for optimizing tumor damage is the schedule for successive administrations of the AdfVII/IgG(1)Fc, which should coincide with the regeneration of the peripheral vasculature and continue until the tumor is destroyed.

Indexed as

AdenoviridaeAnimalsBiomarkers, TumorBreast NeoplasmsEndothelial CellsEndothelium, VascularGenetic VectorsHumansImmunoconjugatesImmunotherapyMiceNeovascularization, PathologicPlatelet Endothelial Cell Adhesion Molecule-1Receptor, TIE-1Spheroids, CellularThromboplastinBiomarkers, TumorImmunoconjugatesPlatelet Endothelial Cell Adhesion Molecule-1Receptor, TIE-1Thromboplastin

Identifiers

PMID17235351
OpenAlexW1975185686

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.