Evidence map›Paper›PMID 25292427›Full record

ReviewAnnual review of pharmacology and toxicology2015

Eph receptors and ephrins: therapeutic opportunities.

Antonio Barquilla, Elena B Pasquale

Open access · bronzeAbstract readReview
In one paragraph

Review in Annual review of pharmacology and toxicology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 186 papers.

0numbers the graph read from it
0cells of the map it votes in
186citing papers in PubMed
8.7field-weighted citation impact, top 1% 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

186 citing papers in PubMed, 311 citations in OpenAlex.

  1. Article
  2. Review
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  11. Design and Evaluation of EbCancer science · 2025
    Article
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  18. Astrocytic EphA4 signaling is important for the elimination of excitatory synapses in Alzheimer's disease.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  19. Article
  20. Article

126 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

2 authors at 2 institutions in 1 country.

Antonio BarquillaCancer Center, Sanford-Burnham Medical Research Institute, La Jolla, California 92037; email: abarquilla@sanfordburnham.org , elenap@sanfordburnham.org.
Elena B Pasquale
Sanford Burnham Prebys Medical Discovery Institute · USUniversity of California, San Diego · US

Funding

Tumor Microenvironment and Cancer ImmunologyP30CA030199 · NCI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI Jianhua Zhao · 1985 to 2026
$107.2M
Targeting Eph receptors in cancerP01CA138390 · NCI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI PASQUALE, ELENA B · 2010 to 2014
$7.3M
Cyclic EphA4 peptide antagonists for neuroprotection in ALSR01NS087070 · NINDS · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI PASQUALE, ELENA B · 2014 to 2018
$3.5M
Structure and Function of BCAR1 and BCAR3 Association in Breast Cancer MalignancyR01CA160457 · NCI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI PASQUALE, ELENA B, RIEDL, STEFAN J · 2011 to 2015
$2.2M
Functional landscape of Eph receptor mutations in melanomaR21CA175881 · NCI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI PASQUALE, ELENA B · 2014 to 2015
$467k
NCI NIH HHS P01 CA138390NCI NIH HHS P30 CA030199NCI NIH HHS R01 CA160457NCI NIH HHS R21 CA175881NINDS NIH HHS R01 NS087070
6 · The paper itself

Abstract

The erythropoietin-producing hepatocellular carcinoma (Eph) receptor tyrosine kinase family plays important roles in developmental processes, adult tissue homeostasis, and various diseases. Interaction with Eph receptor-interacting protein (ephrin) ligands on the surface of neighboring cells triggers Eph receptor kinase-dependent signaling. The ephrins can also transmit signals, leading to bidirectional cell contact-dependent communication. Moreover, Eph receptors and ephrins can function independently of each other through interplay with other signaling systems. Given their involvement in many pathological conditions ranging from neurological disorders to cancer and viral infections, Eph receptors and ephrins are increasingly recognized as attractive therapeutic targets, and various strategies are being explored to modulate their expression and function. Eph receptor/ephrin upregulation in cancer cells, the angiogenic vasculature, and injured or diseased tissues also offer opportunities for Eph/ephrin-based targeted drug delivery and imaging. Thus, despite the challenges presented by the complex biology of the Eph receptor/ephrin system, exciting possibilities exist for therapies exploiting these molecules.

Indexed as

Drug DesignAnimalsAntineoplastic AgentsAntiviral AgentsCardiovascular AgentsCardiovascular DiseasesEphrinsHumansLigandsMolecular Targeted TherapyNeoplasmsNervous System DiseasesReceptors, Eph FamilySignal TransductionVirus DiseasesAntineoplastic AgentsAntiviral AgentsCardiovascular AgentsEphrinsLigandsReceptors, Eph Familyangiogenesiscancerneurological diseasetyrosine kinaseviral infection

Identifiers

PMID25292427
PMCPMC4388660
OpenAlexW2096043623

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.