Evidence map›Paper›PMID 19965691›Full record

ArticleBlood2010

Vascular endothelial growth factor activation of endothelial cells is mediated by early growth response-3.

Jun-ichi Suehiro, Takao Hamakubo, Tatsuhiko Kodama, William C Aird, Takashi Minami

Open access · greenAbstract read
In one paragraph

Article in Blood, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

45 citing papers in PubMed, 109 citations in OpenAlex.

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  12. Inducible CRISPR Epigenome Systems Mimic Cocaine Induced Bidirectional Regulation of Nab2 and Egr3.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
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  18. Role of NFAT in the Progression of Diabetic Atherosclerosis.Frontiers in cardiovascular medicine · 2021
    Review
  19. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 2 countries.

Jun-ichi SuehiroResearch Center for Advanced Science and Technology, The University of Tokyo, Tokyo 153-8904, Japan.
Takao Hamakubo
Tatsuhiko Kodama
William C Aird
Takashi Minami
The University of Tokyo · JPBeth Israel Deaconess Medical Center · US

Funding

VASCULAR TOPOGRAPHY OF CD39/NTPDASESP01HL076540 · NHLBI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI AIRD, WILLIAM C · 2004 to 2014
$20.3M
VEGF, Transcriptional Networks and Vascular InflammationR01HL082927 · NHLBI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI AIRD, WILLIAM C · 2007 to 2010
$1.5M
NHLBI NIH HHS HL076540NHLBI NIH HHS HL082927NHLBI NIH HHS P01 HL076540NHLBI NIH HHS R01 HL082927
6 · The paper itself

Abstract

Endothelial cell activation and dysfunction underlie many vascular disorders, including atherosclerosis, tumor growth, and sepsis. Endothelial cell activation, in turn, is mediated primarily at the level of gene transcription. Here, we show that in response to several activation agonists, including vascular endothelial growth factor (VEGF), tumor necrosis factor-alpha, and thrombin, endothelial cells demonstrate rapid and profound induction of the early growth response (Egr) genes egr-1 and egr-3. In VEGF-treated endothelial cells, induction of Egr-3 was far greater and more prolonged compared with Egr-1. VEGF-mediated stimulation of Egr-3 involved the inducible binding of NFATc, serum response factor, and CREB to their respective consensus motifs in the upstream promoter region of Egr-3. Knockdown of Egr-3 markedly impaired VEGF-mediated proliferation, migration, and tube formation of endothelial cells and blocked VEGF-induced monocyte adhesion. Egr-3 knockdown abrogated VEGF-mediated vascular outgrowth from ex vivo aortic rings and attenuated Matrigel plug vascularization and melanoma tumor growth in vivo. Together, these findings suggest that Egr-3 is a critical determinant of VEGF signaling in activated endothelial cells. Thus, Egr-3 represents a potential therapeutic target in VEGF-mediated vasculopathic diseases.

Indexed as

AnimalsCell DivisionCell MovementCells, CulturedCoronary VesselsCyclic AMP Response Element-Binding ProteinEarly Growth Response Protein 1Early Growth Response Protein 3Endothelial CellsHumansMelanomaMiceMice, Inbred C57BLNeovascularization, PathologicNFATC Transcription FactorsPulmonary ArteryCREB1 protein, humanCyclic AMP Response Element-Binding ProteinEarly Growth Response Protein 1Early Growth Response Protein 3EGR1 protein, humanEGR3 protein, humanNFATC1 protein, humanNFATC Transcription FactorsSerum Response FactorSRF protein, humanThrombinTumor Necrosis Factor-alphaVascular Endothelial Growth Factor AVEGFA protein, human

Identifiers

PMID19965691
PMCPMC2845904
OpenAlexW2009096648

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.