Evidence map›Paper›PMID 30037214›Full record

ArticleMolecules and cells2018

Oleanolic Acids Inhibit Vascular Endothelial Growth Factor Receptor 2 Signaling in Endothelial Cells: Implication for Anti-Angiogenic Therapy.

Da-Hye Lee, Jungsul Lee, Jongwook Jeon, Kyung-Jin Kim, Jang-Hyuk Yun, Han-Seok Jeong, Eun Hui Lee, Young Jun Koh, Chung-Hyun Cho

Open access · greenAbstract read
In one paragraph

Article in Molecules and cells, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

11 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
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  7. Antiproliferative Activity ofPharmaceuticals (Basel, Switzerland) · 2022
    Article
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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

9 authors at 4 institutions in 1 country.

Da-Hye LeeVascular Microenvironment Laboratory, Department of Pharmacology and Ischemic/Hypoxic Disease Institute, College of Medicine, Seoul National University, Seoul 03080, Korea.
Jungsul LeeDepartment of Bio and Brain Engineering, KAIST, Daejeon 34141, Korea.
Jongwook JeonThe Korean Research Institute of Science, Technology and Civilization, Chonbuk National University, Jeonju 54896, Korea.
Kyung-Jin KimVascular Microenvironment Laboratory, Department of Pharmacology and Ischemic/Hypoxic Disease Institute, College of Medicine, Seoul National University, Seoul 03080, Korea.
Jang-Hyuk YunVascular Microenvironment Laboratory, Department of Pharmacology and Ischemic/Hypoxic Disease Institute, College of Medicine, Seoul National University, Seoul 03080, Korea.
Han-Seok JeongVascular Microenvironment Laboratory, Department of Pharmacology and Ischemic/Hypoxic Disease Institute, College of Medicine, Seoul National University, Seoul 03080, Korea.
Eun Hui LeeDepartment of Physiology, College of Medicine, The Catholic University of Korea, Seoul 06591, Korea.
Young Jun KohDepartment of Pathology, College of Korean Medicine, Dongguk University, Goyang 10326, Korea.
Chung-Hyun ChoVascular Microenvironment Laboratory, Department of Pharmacology and Ischemic/Hypoxic Disease Institute, College of Medicine, Seoul National University, Seoul 03080, Korea.
Seoul National University · KRCatholic University of Korea · KRDongguk University · KRKorea Institute of Brain Science · KR

Funding

National Research Foundation of Korea 2012R1A5A2A44671346National Research Foundation of Korea 2017R1C1B2005982SNUH Research Fund 0420180470
6 · The paper itself

Abstract

Angiogenesis must be precisely controlled because uncontrolled angiogenesis is involved in aggravation of disease symptoms. Vascular endothelial growth factor (VEGF)/VEGF receptor 2 (VEGFR-2) signaling is a key pathway leading to angiogenic responses in vascular endothelial cells (ECs). Therefore, targeting VEGF/VEGFR-2 signaling may be effective at modulating angiogenesis to alleviate various disease symptoms. Oleanolic acid was verified as a VEGFR-2 binding chemical from anticancer herbs with similar binding affinity as a reference drug in the Protein Data Bank (PDB) entry 3CJG of model A coordination. Oleanolic acid effectively inhibited VEGF-induced VEGFR-2 activation and angiogenesis in HU-VECs without cytotoxicity. We also verified that oleanolic acid inhibits

Indexed as

Angiogenesis InhibitorsAnimalsHumansHuman Umbilical Vein Endothelial CellsMiceMice, Inbred C57BLNeovascularization, PhysiologicOleanolic AcidRecombinant ProteinsRetinal NeovascularizationSignal TransductionVascular Endothelial Growth Factor AVascular Endothelial Growth Factor Receptor-2Angiogenesis InhibitorsKdr protein, mouseOleanolic AcidRecombinant ProteinsVascular Endothelial Growth Factor AVascular Endothelial Growth Factor Receptor-2VEGFA protein, humanangiogenesisendothelial cellsoleanolic acidretinopathy of prematurityVEGFR-2

Identifiers

PMID30037214
PMCPMC6125422
OpenAlexW2919702421

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.