Evidence map›Paper›PMID 18981713›Full record

ArticleCancer biology & therapy2008

Activated STAT3 is a mediator and biomarker of VEGF endothelial activation.

Shao-Hua Chen, Danielle A Murphy, Wiem Lassoued, Gavin Thurston, Michael D Feldman, William M F Lee

Open access · bronzeAbstract read
In one paragraph

Article in Cancer biology & therapy, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed, 2 pooled it
2.9field-weighted citation impact, top 9% 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

78 citing papers in PubMed, 2 syntheses or guidelines pooled it, 131 citations in OpenAlex.

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  14. CombinationThyroid : official journal of the American Thyroid Association · 2023
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18 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Shao-Hua ChenDepartment of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Danielle A Murphy
Wiem Lassoued
Gavin Thurston
Michael D Feldman
William M F Lee
University of Pennsylvania · US

Funding

TRANSGENIC AND CHIMERIC MOUSE COREP30DK050306 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI Ken Hashigiwa Cadwell · 1997 to 2026
$32.5M
Transgenic Mice as Models for Antivascular TherapyR01CA099519 · NCI · UNIVERSITY OF PENNSYLVANIA · PI LEE, WILLIAM M · 2003 to 2007
$1.7M
MECHANISMS OF TUMOR REJECTIONR01CA077851 · NCI · UNIVERSITY OF PENNSYLVANIA · PI LEE, WILLIAM M · 1998 to 2007
$1.7M
Determinants of response to bevacizumab in colon cancerR21CA111874 · NCI · UNIVERSITY OF PENNSYLVANIA · PI O'DWYER, PETER J. · 2005 to 2006
$273k
NCI NIH HHS R01 CA077851NCI NIH HHS R01 CA099519NCI NIH HHS R01 CA77851NCI NIH HHS R01 CA99519NCI NIH HHS R21 CA111874NIDDK NIH HHS P30 DK050306NIDDK NIH HHS P30 DK50306
6 · The paper itself

Abstract

STAT3 plays important roles in cell proliferation and survival signaling and is often constitutively activated in transformed cells. In this study, we examined STAT3 activation in endothelial cells (EC) during angiogenic activation and therapeutic angiogenesis inhibition. VEGF stimulation of cultured EC induced STAT3 phosphorylation by a VEGFR2- and Src-dependent mechanism. FGF2 but not PlGF also induced EC STAT3 activation in vitro. Activated STAT3 mediated VEGF induction of EC Bcl-2 and contributed to VEGF protection of EC from apoptosis. In vivo, p-STAT3 was absent by immunohistological staining in the vascular EC of most normal mouse organs but was present in the vessels of mouse and human tumors. Tumor vascular p-STAT3 increased as tumors were induced to overexpress VEGF, indicating that VEGF is an activator of EC p-STAT3 in vivo. Tumor vascular p-STAT3 decreased during angiogenesis inhibition by antagonists of VEGF-VEGFR signaling, VEGF Trap and SU5416, indicating that VEGF contributed to the EC STAT3 activation seen in the tumors prior to treatment and that p-STAT3 may be used to monitor therapy. These studies show that p-STAT3 is a mediator and biomarker of endothelial activation that reports VEGF-VEGFR2 activity and may be useful for studying the pharmacodynamics of targeted angiogenesis inhibitors.

Indexed as

Angiogenesis InhibitorsAnimalsBiomarkersCell DivisionCell SurvivalEndothelium, VascularHumansMiceMice, Inbred StrainsNeoplasmsNeovascularization, PathologicNeovascularization, PhysiologicSignal TransductionSTAT3 Transcription FactorUmbilical VeinsVascular Endothelial Growth Factor AAngiogenesis InhibitorsBiomarkersSTAT3 protein, humanSTAT3 Transcription FactorVascular Endothelial Growth Factor AVascular Endothelial Growth Factor Receptor-2

Identifiers

PMID18981713
PMCPMC2932444
OpenAlexW1973009607

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.