Evidence map›Paper›PMID 11593034›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2001

Targeting tissue factor on tumor vascular endothelial cells and tumor cells for immunotherapy in mouse models of prostatic cancer.

Z Hu, A Garen

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
3.9field-weighted citation impact, top 7% 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

49 citing papers in PubMed, 108 citations in OpenAlex.

  1. L-ICON3 Suppresses Endometriosis in a Murine Model.Journal of molecular medicine (Berlin, Germany) · 2026
    Article
  2. Review
  3. Review
  4. Review
  5. Tissue factor: a neglected role in cancer biology.Journal of thrombosis and thrombolysis · 2022
    Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Tissue Factor and Cancer: Regulation, Tumor Growth, and Metastasis.Seminars in thrombosis and hemostasis · 2019
    Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. ImmunoPET imaging of tissue factor expression in pancreatic cancer withJournal of controlled release : official journal of the Controlled Release Society · 2017
    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

2 authors at 1 institution in 1 country.

Z HuDepartment of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT 06520, USA.
A Garen
Yale University · US

Funding

TISSUE FACTOR IN BLOOD COAGULATIONP01HL029019 · NHLBI · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI GUHA, ARABINDA · 1985 to 2002
$5.8M
Inhibiting Corneal Neovascularization by Targeting Tissue FactorR21EY037451 · NEI · OHIO STATE UNIVERSITY · PI HU, ZHIWEI, ZHU, HUA · 2025 to 2025
$433k
NEI NIH HHS R21 EY037451NHLBI NIH HHS HL29019NHLBI NIH HHS P01 HL029019
6 · The paper itself

Abstract

The efficacy and safety of an immunoconjugate (icon) molecule, composed of a mutated mouse factor VII (mfVII) targeting domain and the Fc effector domain of an IgG1 Ig (mfVII/Fc icon), was tested with a severe combined immunodeficient (SCID) mouse model of human prostatic cancer and an immunocompetent mouse model of mouse prostatic cancer. The SCID mice were first injected s.c. with a human prostatic tumor line, forming a skin tumor that produces a high blood titer of prostate-specific antigen and metastasizes to bone. The icon was encoded in a replication-incompetent adenoviral vector that was injected directly into the skin tumor. The tumor cells infected by the vector synthesize and secrete the icon into the blood, and the blood-borne icon binds with high affinity and specificity to mouse tissue factor expressed on endothelial cells lining the lumen of the tumor vasculature and to human tissue factor expressed on the tumor cells. The Fc domain of the icon activates a cytolytic immune attack against cells that bind the icon. The immunotherapy tests in SCID mice demonstrated that intratumoral injections of the adenoviral vector encoding the mfVII/human Fc icon resulted in long-term regression of the injected human prostatic tumor and also of a distant uninjected tumor, without associated toxicity to the mice. Comparable results were obtained with a SCID mouse model of human melanoma. At the end of the experiments the mice appeared to be free of viable tumor cells. This protocol also could be efficacious for treating cancer patients who have vascularized tumors.

Indexed as

AnimalsBlood CoagulationCHO CellsConsumer Product SafetyCricetinaeDisease Models, AnimalEndothelium, VascularFactor VIIGene TargetingHemorrhageHumansImmunocompetenceImmunoconjugatesImmunoglobulin Fc FragmentsImmunotherapyMaleFactor VIIImmunoconjugatesImmunoglobulin Fc Fragments

Identifiers

PMID11593034
PMCPMC59788
OpenAlexW1971214445

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.