Evidence map›Paper›PMID 29669933›Full record

ArticleJCI insight2018

Requisite endothelial reactivation and effective siRNA nanoparticle targeting of Etv2/Er71 in tumor angiogenesis.

Ashraf Ul Kabir, Tae-Jin Lee, Hua Pan, Jeffrey C Berry, Karen Krchma, Jun Wu, Fang Liu, Hee-Kyoung Kang, Kristina Hinman, Lihua Yang and 7 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

18 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
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  9. Review
  10. Article
  11. Article
  12. Article
  13. Dual role of endothelialScience translational medicine · 2021
    Article
  14. cAMP/EPAC Signaling Enables ETV2 to Induce Endothelial Cells with High Angiogenesis Potential.Molecular therapy : the journal of the American Society of Gene Therapy · 2020
    Article
  15. NF-κB Inhibition Suppresses Experimental Melanoma Lung Metastasis.Journal of cancer science and clinical therapeutics · 2020
    Article
  16. Article
  17. Article
  18. Review
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

17 authors at 3 institutions in 2 countries.

Ashraf Ul KabirDepartment of Pathology and Immunology and.
Tae-Jin LeeDepartment of Pathology and Immunology and.
Hua PanHealth Heart Institute, Morsani College of Medicine, University of South Florida, Tampa, Florida, USA.
Jeffrey C BerryDepartment of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Karen KrchmaDepartment of Pathology and Immunology and.
Jun WuDepartment of Pathology and Immunology and.
Fang LiuDepartment of Pathology and Immunology and.
Hee-Kyoung KangDepartment of Pharmacology, School of Medicine, Jeju National University, Jeju, South Korea.
Kristina HinmanDepartment of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, Missouri, USA.
Lihua YangDepartment of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Samantha HamiltonDepartment of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Qingyu ZhouDepartment of Pharmaceutical Science, College of Pharmacy, University of South Florida, Tampa, Florida, USA.
Deborah J VeisDepartment of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Robert P MechamDepartment of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, Missouri, USA.
Samuel A WicklineHealth Heart Institute, Morsani College of Medicine, University of South Florida, Tampa, Florida, USA.
Mark J MillerDepartment of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Kyunghee ChoiDepartment of Pathology and Immunology and.
Washington University in St. Louis · USUniversity of South Florida · USJeju National University · KR

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI TIMOTHY J. EBERLEIN · 2001 to 2026
$128.0M
METHODS IN MOLECULAR IMAGING AND TARGETED THERAPEUTICSR01HL073646 · NHLBI · WASHINGTON UNIVERSITY · PI WICKLINE, SAMUEL A · 2004 to 2016
$13.7M
Hemangioglast Development and RegulationR01HL055337 · NHLBI · WASHINGTON UNIVERSITY · PI CHOI, KYUNGHEE · 2001 to 2024
$9.1M
HEMATOPOIETIC COMMITMENT: MOLECULAR MECHANISMSR01HL063736 · NHLBI · WASHINGTON UNIVERSITY · PI CHOI, KYUNGHEE · 2000 to 2016
$5.6M
Epithelial Responses to Bacterial InvasionR01AI077600 · NIAID · WASHINGTON UNIVERSITY · PI MILLER, MARK JAMES · 2009 to 2021
$3.8M
ASSEMBLY OF LUNG ELASTINR01HL053325 · NHLBI · WASHINGTON UNIVERSITY · PI MECHAM, ROBERT P. · 1995 to 2019
$3.6M
VESSEL STIFFENING, HYPERTENSION, AND VASCULAR EXTRACELLULAR MATRIXR01HL105314 · NHLBI · WASHINGTON UNIVERSITY · PI MECHAM, ROBERT P., WAGENSEIL, JESSICA · 2010 to 2018
$3.2M
Prevention and Treatment of Acute Kidney InjuryR01DK102691 · NIDDK · WASHINGTON UNIVERSITY · PI WICKLINE, SAMUEL A · 2015 to 2018
$2.0M
Inhibition of NF-kB with siRNA/Peptide Nanoparticles for Arthritis TreatmentR01AR067491 · NIAMS · WASHINGTON UNIVERSITY · PI PHAM, CHRISTINE T., WICKLINE, SAMUEL A · 2015 to 2019
$1.8M
Role of Mitochondrial Dynamics In Bone HomeostasisR01AR070030 · NIAMS · WASHINGTON UNIVERSITY · PI VEIS, DEBORAH J · 2016 to 2020
$1.8M
NCI NIH HHS P30 CA091842NHLBI NIH HHS R01 HL055337NHLBI NIH HHS R01 HL063736NHLBI NIH HHS R01 HL073646NHLBI NIH HHS R01 HL105314NIAID NIH HHS R01 AI077600NIAMS NIH HHS R01 AR067491NIDDK NIH HHS R01 DK102691
6 · The paper itself

Abstract

Angiogenesis, new blood vessel formation from preexisting vessels, is critical for solid tumor growth. As such, there have been efforts to inhibit angiogenesis as a means to obstruct tumor growth. However, antiangiogenic therapy faces major challenges to the selective targeting of tumor-associated-vessels, as current antiangiogenic targets also disrupt steady-state vessels. Here, we demonstrate that the developmentally critical transcription factor Etv2 is selectively upregulated in both human and mouse tumor-associated endothelial cells (TAECs) and is required for tumor angiogenesis. Two-photon imaging revealed that Etv2-deficient tumor-associated vasculature remained similar to that of steady-state vessels. Etv2-deficient TAECs displayed decreased Flk1 (also known as Vegfr2) expression, FLK1 activation, and proliferation. Endothelial tube formation, proliferation, and sprouting response to VEGF, but not to FGF2, was reduced in Etv2-deficient ECs. ROS activated Etv2 expression in ECs, and ROS blockade inhibited Etv2 expression in TAECs in vivo. Systemic administration of Etv2 siRNA nanoparticles potently inhibited tumor growth and angiogenesis without cardiovascular side effects. These studies highlight a link among vascular oxidative stress, Etv2 expression, and VEGF response that is critical for tumor angiogenesis. Targeting the ETV2 pathway might offer a unique opportunity for more selective antiangiogenic therapies.

Indexed as

AnimalsEndothelial CellsFemaleFibroblast Growth Factor 2Genetic TherapyHumansMaleMiceMice, Inbred C57BLNanoparticlesNeovascularization, PathologicOxidative StressRNA, Small InterferingTranscription FactorsUp-RegulationVascular Endothelial Growth Factor AER71 protein, mouseETV2 protein, humanFibroblast Growth Factor 2RNA, Small InterferingTranscription FactorsVascular Endothelial Growth Factor AVascular Endothelial Growth Factor Receptor-2AngiogenesisCancer gene therapyendothelial cellshypoxia

Identifiers

PMID29669933
PMCPMC5931123
OpenAlexW2799406907

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.