Evidence map›Paper›PMID 30036530›Full record

ArticleJournal of theoretical biology2018

Computational modeling of synergistic interaction between αVβ3 integrin and VEGFR2 in endothelial cells: Implications for the mechanism of action of angiogenesis-modulating integrin-binding peptides.

Hojjat Bazzazi, Yu Zhang, Mohammad Jafarnejad, Aleksander S Popel

Open access · bronzeAbstract read
In one paragraph

Article in Journal of theoretical biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

14 citing papers in PubMed, 24 citations in OpenAlex.

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  11. [Effect of demineralized bone matrix modified by laminin α4 chain functional peptide on H-type angiogenesis and osteogenesis to promote bone defect repair].Zhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery · 2020
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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

4 authors at 1 institution in 1 country.

Hojjat BazzaziDepartment of Biomedical Engineering, School of Medicine, Johns Hopkins University, Baltimore, MD 21205, United States.
Yu ZhangDepartment of Biomedical Engineering, School of Medicine, Johns Hopkins University, Baltimore, MD 21205, United States. Electronic address: zhangyu@jhmi.edu.
Mohammad JafarnejadDepartment of Biomedical Engineering, School of Medicine, Johns Hopkins University, Baltimore, MD 21205, United States.
Aleksander S PopelDepartment of Biomedical Engineering, School of Medicine, Johns Hopkins University, Baltimore, MD 21205, United States.
Johns Hopkins University · US

Funding

Systems Biology of Angiogenesis in Peripheral Arterial DiseaseR01HL101200 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI POPEL, ALEKSANDER S. · 2010 to 2022
$10.7M
Predictive experiment-based multiscale models of the tumor immune microenvironment and immunotherapy in breast cancerR01CA138264 · NCI · JOHNS HOPKINS UNIVERSITY · PI POPEL, ALEKSANDER S. · 2009 to 2023
$8.1M
Sustained Suprachoroidal Delivery of Therapeutic Peptidesfor Ocular DiseasesR21EY026148 · NEI · JOHNS HOPKINS UNIVERSITY · PI CAMPOCHIARO, PETER A, GREEN, JORDAN · 2016 to 2017
$449k
NCI NIH HHS R01 CA138264NEI NIH HHS R21 EY026148NHLBI NIH HHS R01 HL101200
6 · The paper itself

Abstract

Cooperation between VEGFR2 and integrin αVβ3 is critical for neovascularization in wound healing, cardiovascular ischemic diseases, ocular diseases, and tumor angiogenesis. In the present study, we developed a rule-based computational model to investigate the potential mechanism by which the Src-induced integrin association with VEGFR2 enhances VEGFR2 activation. Simulations demonstrated that the main function of integrin is to reduce the degradation of VEGFR2 and hence stabilize the activation signal. In addition, receptor synthesis rate and recruitment from internal compartment were found to be sensitive determinants of the activation state of VEGFR2. The model was then applied to simulate the effect of integrin-binding peptides such as tumstatin and cilengitide on VEGFR2 signaling. Further, computational modeling proposed potential molecular mechanisms for the angiogenesis-modulating activity of other integrin-binding peptides. The model highlights the complexity of the crosstalk between αVβ3 integrin and VEGFR2 and the necessity of utilizing models to elucidate potential mechanisms in angiogenesis-modulating peptide therapy.

Indexed as

AutoantigensCollagen Type IVModels, BiologicalNeovascularization, PathologicSnake VenomsEndothelial CellsHumansIntegrin alphaVbeta3Neoplasm ProteinsNeoplasmsSignal TransductionVascular Endothelial Growth Factor Receptor-2AutoantigensCilengitideCollagen Type IVIntegrin alphaVbeta3KDR protein, humanNeoplasm ProteinsSnake Venomstype IV collagen alpha3 chainVascular Endothelial Growth Factor Receptor-2Computational modelIntegrin signalingMathematical modelSystems biologyVEGF

Identifiers

PMID30036530
PMCPMC6156791
OpenAlexW2883161420

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.