Evidence map›Paper›PMID 23871637›Full record

ArticleCancer cell2013

A core human primary tumor angiogenesis signature identifies the endothelial orphan receptor ELTD1 as a key regulator of angiogenesis.

Massimo Masiero, Filipa Costa Simões, Hee Dong Han, Cameron Snell, Tessa Peterkin, Esther Bridges, Lingegowda S Mangala, Sherry Yen-Yao Wu, Sunila Pradeep, Demin Li and 11 more

Open access · hybridAbstract read
In one paragraph

Article in Cancer cell, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 219 papers.

0numbers the graph read from it
0cells of the map it votes in
219citing papers in PubMed
6.4field-weighted citation impact, top 3% 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

219 citing papers in PubMed, 309 citations in OpenAlex.

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  13. Adhesion G protein-coupled receptors.Pharmacological reviews · 2026
    Review
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  19. Dual regulation of autophagy: paradoxical effects on tumor angiogenesis.Frontiers in cell and developmental biology · 2026
    Review
  20. Article

159 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

21 authors at 4 institutions in 2 countries.

Massimo MasieroNuffield Division of Clinical Laboratory Sciences, Radcliffe Department of Medicine, John Radcliffe Hospital, Headington, Oxford OX3 9DU, UK.
Filipa Costa Simões
Hee Dong Han
Cameron Snell
Tessa Peterkin
Esther Bridges
Lingegowda S Mangala
Sherry Yen-Yao Wu
Sunila Pradeep
Demin Li
Cheng Han
Heather Dalton
Gabriel Lopez-Berestein
Jurriaan B Tuynman
Neil Mortensen
Ji-Liang Li
Roger Patient
Anil K Sood
Alison H Banham
Adrian L Harris
Francesca M Buffa
The University of Texas MD Anderson Cancer Center · USJohn Radcliffe Hospital · GBMRC Weatherall Institute of Molecular Medicine · GBCancer Research UK · GB

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
UNIVERSITY OF TEXAS MD ANDERSON SPORE IN OVARIAN CANCERP50CA083639 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI BAST, ROBERT C · 1999 to 2015
$33.0M
Targeting the PI3K Signaling Pathway in Endometrial CarcinomaP50CA098258 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI BODURKA, DIANE · 2003 to 2020
$32.0M
Texas Center for Cancer NanomedicineU54CA151668 · NCI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI FERRARI, MAURO · 2010 to 2014
$12.4M
British Heart Foundation PG/09/082/28020Cancer Research UK 10702Cancer Research UK A10702Medical Research Council MC_U137981013Medical Research Council MC_UU_12009/8NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA083639NCI NIH HHS P50 CA098258NCI NIH HHS P50CA098258NCI NIH HHS U54 CA151668
6 · The paper itself

Abstract

Limited clinical benefits derived from anti-VEGF therapy have driven the identification of new targets involved in tumor angiogenesis. Here, we report an integrative meta-analysis to define the transcriptional program underlying angiogenesis in human cancer. This approach identified ELTD1, an orphan G-protein-coupled receptor whose expression is induced by VEGF/bFGF and repressed by DLL4 signaling. Extensive analysis of multiple cancer types demonstrates significant upregulation of ELTD1 in tumor-associated endothelial cells, with a higher expression correlating with favorable prognosis. Importantly, ELTD1 silencing impairs endothelial sprouting and vessel formation in vitro and in vivo, drastically reducing tumor growth and greatly improving survival. Collectively, these results provide insight into the regulation of tumor angiogenesis and highlight ELTD1 as key player in blood vessel formation.

Indexed as

AnimalsCell Growth ProcessesEndothelial CellsFemaleGenetic Predisposition to DiseaseHCT116 CellsHumansMiceMice, NudeNeoplasmsNeovascularization, PathologicReceptors, G-Protein-CoupledSignal TransductionADGRL4 protein, humanReceptors, G-Protein-Coupled

Identifiers

PMID23871637
PMCPMC3743050
OpenAlexW2097177355

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.