Evidence map›Paper›PMID 25278287›Full record

ReviewArteriosclerosis, thrombosis, and vascular biology2015

Canonical and noncanonical vascular endothelial growth factor pathways: new developments in biology and signal transduction.

Courtney K Domigan, Safiyyah Ziyad, M Luisa Iruela-Arispe

Open access · bronzeAbstract readReview
In one paragraph

Review in Arteriosclerosis, thrombosis, and vascular biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

35 citing papers in PubMed, 58 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Review
  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

3 authors at 2 institutions in 1 country.

Courtney K DomiganFrom the Department of Molecular, Cell, and Developmental Biology (C.K.D., S.Z., M.L.I.-A.), Molecular Biology Institute (M.L.I.-A.), and Jonsson Comprehensive Cancer Center (M.L.I.-A.), University of California, Los Angeles.
Safiyyah ZiyadFrom the Department of Molecular, Cell, and Developmental Biology (C.K.D., S.Z., M.L.I.-A.), Molecular Biology Institute (M.L.I.-A.), and Jonsson Comprehensive Cancer Center (M.L.I.-A.), University of California, Los Angeles.
M Luisa Iruela-ArispeFrom the Department of Molecular, Cell, and Developmental Biology (C.K.D., S.Z., M.L.I.-A.), Molecular Biology Institute (M.L.I.-A.), and Jonsson Comprehensive Cancer Center (M.L.I.-A.), University of California, Los Angeles. arispe@mcdb.ucla.edu.
Molecular Oncology (United States) · USMolecular Medicine Research Institute · US

Funding

UCLA NIGMS T32 Program AssessmentT32GM007185 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI TORRES, JORGE · 1985 to 2020
$21.7M
Vascular Biology Training GrantT32HL069766 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LUSIS, ALDONS JAKE · 2002 to 2022
$7.4M
VEGF Signaling and Tumor MicroenvironmentR01CA126935 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI IRUELA-ARISPE, M. LUISA · 2007 to 2011
$1.4M
NCI NIH HHS R01 CA126935NCI NIH HHS R01CA126935NHLBI NIH HHS T32 HL069766NHLBI NIH HHS T32 HL69766NIGMS NIH HHS T32 GM007185
6 · The paper itself

Abstract

The past 5 years have witnessed a significant expansion in our understanding of vascular endothelial growth factor (VEGF) signaling. In particular, the process of canonical activation of VEGF receptor tyrosine kinases by homodimeric VEGF molecules has now been broadened by the realization that heterodimeric ligands and receptors are also active participants in the signaling process. Although heterodimer receptors were described 2 decades ago, their impact, along with the effect of additional cell surface partners and novel autocrine VEGF signaling pathways, are only now starting to be clarified. Furthermore, ligand-independent signaling (noncanonical) has been identified through galectin and gremlin binding and upon rise of intracellular levels of reactive oxygen species. Activation of the VEGF receptors in the absence of ligand holds immediate implications for therapeutic approaches that exclusively target VEGF. The present review provides a concise summary of the recent developments in both canonical and noncanonical VEGF signaling and places these findings in perspective to their potential clinical and biological ramifications.

Indexed as

Signal TransductionAngiogenesis Modulating AgentsAnimalsAutocrine CommunicationGalectinsHumansIntercellular Signaling Peptides and ProteinsLigandsNeovascularization, PathologicNeovascularization, PhysiologicProtein ConformationProtein MultimerizationReceptors, Vascular Endothelial Growth FactorVascular Endothelial Growth Factor AAngiogenesis Modulating AgentsGalectinsGREM1 protein, humanIntercellular Signaling Peptides and ProteinsLigandsReceptors, Vascular Endothelial Growth FactorVascular Endothelial Growth Factor Aendothelial cells

Identifiers

PMID25278287
PMCPMC4270848
OpenAlexW2524178063

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.