Evidence map›Paper›PMID 12370823›Full record

ArticleOncogene2002

Soluble Eph A receptors inhibit tumor angiogenesis and progression in vivo.

Dana M Brantley, Nikki Cheng, Erin J Thompson, Qing Lin, Rolf A Brekken, Philip E Thorpe, Rebecca S Muraoka, Douglas Pat Cerretti, Ambra Pozzi, Dowdy Jackson and 2 more

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 131 papers.

0numbers the graph read from it
0cells of the map it votes in
131citing papers in PubMed
7.2field-weighted citation impact, top 2% 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

131 citing papers in PubMed, 317 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. World journal of gastrointestinal oncology · 2022
    Review
  9. Article
  10. Article
  11. Progranulin/EphA2 axis: A novel oncogenic mechanism in bladder cancer.Matrix biology : journal of the International Society for Matrix Biology · 2020
    Article
  12. Article
  13. Article
  14. Article
  15. Tumor angiogenesis: causes, consequences, challenges and opportunities.Cellular and molecular life sciences : CMLS · 2020
    Review
  16. Cells · 2020
    Article
  17. Article
  18. Article
  19. Therapeutic potential of targeting the Eph/ephrin signaling complex.The international journal of biochemistry & cell biology · 2018
    Review
  20. Review

71 more citing papers are in PubMed but not listed here.

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

12 authors at 5 institutions in 2 countries.

Dana M BrantleyDepartment of Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee, TN 37232, USA.
Nikki Cheng
Erin J Thompson
Qing Lin
Rolf A Brekken
Philip E Thorpe
Rebecca S Muraoka
Douglas Pat Cerretti
Ambra Pozzi
Dowdy Jackson
Charles Lin
Jin Chen
Vanderbilt University · USAmeren (United States) · USHope Heart Institute · USResearch & Development Corporation · CAThe University of Texas Southwestern Medical Center · US

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI MATTHEW J TYSKA · 1995 to 2026
$172.8M
MULTIDISCIPLINARY BASIC RESEARCH TRAINING IN CANCERT32CA009592 · NCI · VANDERBILT UNIVERSITY · PI Justin M Balko, Julie A Rhoades (Sterling) · 1987 to 2026
$10.4M
TRAINING GRANT IN MECHANISMS OF VASCULAR DISEASET32HL007751 · NHLBI · VANDERBILT UNIVERSITY · PI BOCK, PAUL E · 1994 to 2014
$6.6M
ECK RECEPTOR TYROSINE KINASE IN HINDBRAIN DEVELOPMENTR01HD036400 · NICHD · VANDERBILT UNIVERSITY · PI CHEN, JIN · 1999 to 2002
$526k
SIGNALS FOR RENAL ENDOTHELIAL CAPILLARY MORPHOGENESISR01DK047078 · NIDDK · VANDERBILT UNIVERSITY · PI CHEN, JIN · 1994 to 2001
$389k
NCI NIH HHS 2P30CA68485NCI NIH HHS T-32 CA09592NHLBI NIH HHS T32-HL-07751-06NICHD NIH HHS HD36400NIDDK NIH HHS DK47078
6 · The paper itself

Abstract

The Eph family of receptor tyrosine kinases and their ligands, known as ephrins, play a crucial role in vascular development during embryogenesis. The function of these molecules in adult angiogenesis has not been well characterized. Here, we report that blocking Eph A class receptor activation inhibits angiogenesis in two independent tumor types, the RIP-Tag transgenic model of angiogenesis-dependent pancreatic islet cell carcinoma and the 4T1 model of metastatic mammary adenocarcinoma. Ephrin-A1 ligand was expressed in both tumor and endothelial cells, and EphA2 receptor was localized primarily in tumor-associated vascular endothelial cells. Soluble EphA2-Fc or EphA3-Fc receptors inhibited tumor angiogenesis in cutaneous window assays, and tumor growth in vivo. EphA2-Fc or EphA3-Fc treatment resulted in decreased tumor vascular density, tumor volume, and cell proliferation, but increased cell apoptosis. However, EphA2-Fc had no direct effect on tumor cell growth or apoptosis in culture, yet inhibited migration of endothelial cells in response to tumor cells, suggesting that the soluble receptor inhibited blood vessel recruitment by the tumor. These data provide the first functional evidence for Eph A class receptor regulation of pathogenic angiogenesis induced by tumors and support the function of A class Eph receptors in tumor progression.

Indexed as

Adenoma, Islet CellAnimalsCell MovementEndothelial Growth FactorsEndothelium, VascularFemaleIn Situ Nick-End LabelingLymphokinesMammary Neoplasms, ExperimentalMiceMice, Inbred BALB CMice, Inbred C57BLNeoplasms, ExperimentalNeovascularization, PathologicPlatelet Endothelial Cell Adhesion Molecule-1Proliferating Cell Nuclear AntigenEndothelial Growth FactorsLymphokinesPlatelet Endothelial Cell Adhesion Molecule-1Proliferating Cell Nuclear AntigenReceptor, EphA1Receptor, EphA2Receptor Protein-Tyrosine KinasesVascular Endothelial Growth Factor AVascular Endothelial Growth Factors

Identifiers

PMID12370823
OpenAlexW1994137567

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.