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      Ticagrelor Improves Endothelial Function by Decreasing Circulating Epidermal Growth Factor (EGF)

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          Abstract

          Ticagrelor is one of the most powerful P2Y 12 inhibitor. We have recently reported that, in patients with concomitant Stable Coronary Artery Disease (SCAD) and Chronic Obstructive Pulmonary Disease (COPD) undergoing percutaneous coronary intervention (PCI), treatment with ticagrelor, as compared to clopidogrel, is associated with an improvement of the endothelial function (Clinical Trial NCT02519608). In the present study, we showed that, in the same population, after 1 month treatment with ticagrelor, but not with clopidogrel, there is a decrease of the circulating levels of epidermal growth factor (EGF) and that these changes in circulating levels of EGF correlate with on-treatment platelet reactivity. Furthermore, in human umbilical vein endothelial cells (HUVEC) incubated with sera of the patients treated with ticagrelor, but not with clopidogrel there is an increase of p-eNOS levels. Finally, analyzing the changes in EGF and p-eNOS levels after treatment, we observed an inverse correlation between p-eNOS and EGF changes only in the ticagrelor group. Causality between EGF and eNOS activation was assessed in vitro in HUVEC where we showed that EGF decreases eNOS activity in a dose dependent manner. Taken together our data indicate that ticagrelor improves endothelial function by lowering circulating EGF that results in the activation of eNOS in the vascular endothelium.

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          Most cited references31

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          Epidermal growth factor.

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            Heparin-binding EGF-like growth factor and ErbB signaling is essential for heart function.

            The heparin-binding epidermal growth factor (EGF)-like growth factor (HB-EGF) is a member of the EGF family of growth factors that binds to and activates the EGF receptor (EGFR) and the related receptor tyrosine kinase, ErbB4. HB-EGF-null mice (HB(del/del)) were generated to examine the role of HB-EGF in vivo. More than half of the HB(del/del) mice died in the first postnatal week. The survivors developed severe heart failure with grossly enlarged ventricular chambers. Echocardiographic examination showed that the ventricular chambers were dilated and that cardiac function was diminished. Moreover, HB(del/del) mice developed grossly enlarged cardiac valves. The cardiac valve and the ventricular chamber phenotypes resembled those displayed by mice lacking EGFR, a receptor for HB-EGF, and by mice conditionally lacking ErbB2, respectively. HB-EGF-ErbB interactions in the heart were examined in vivo by administering HB-EGF to WT mice. HB-EGF induced tyrosine phosphorylation of ErbB2 and ErbB4, and to a lesser degree, of EGFR in cardiac myocytes. In addition, constitutive tyrosine phosphorylation of both ErbB2 and ErbB4 was significantly reduced in HB(del/del) hearts. It was concluded that HB-EGF activation of receptor tyrosine kinases is essential for normal heart function.
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              Epidermal growth factor, from gene organization to bedside.

              In 1962, epidermal growth factor (EGF) was discovered by Dr. Stanley Cohen while studying nerve growth factor (NGF). It was soon recognized that EGF is the prototypical member of a family of peptide growth factors that activate the EGF receptors, and that the EGF/EGF receptor signaling pathway plays important roles in proliferation, differentiation and migration of a variety of cell types, especially in epithelial cells. After the basic characterization of EGF function in the first decade or so after its discovery, the studies related to EGF and its signaling pathway have extended to a broad range of investigations concerning its biological and pathophysiological roles in development and in human diseases. In this review, we briefly describe the gene organization and tissue distribution of EGF, with emphasis on its biological and pathological roles in human diseases.
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                Author and article information

                Contributors
                Journal
                Front Physiol
                Front Physiol
                Front. Physiol.
                Frontiers in Physiology
                Frontiers Media S.A.
                1664-042X
                06 April 2018
                2018
                : 9
                : 337
                Affiliations
                [1] 1Department of Medical Sciences, University of Ferrara , Ferrara, Italy
                [2] 2Maria Cecilia Hospital, GVM Care & Research, E.S. Health Science Foundation , Cotignola, Italy
                [3] 3Department of Morphology, Surgery and Experimental Medicine, University of Ferrara , Ferrara, Italy
                [4] 4Cardiovascular Institute, Azienda Ospedaliero-Universitaria di Ferrara , Cona, Italy
                [5] 5Laboratory for Technologies of Advanced Therapies, University of Ferrara , Ferrara, Italy
                Author notes

                Edited by: Pasquale Pagliaro, Università degli Studi di Torino, Italy

                Reviewed by: Marco Moscarelli, Imperial College London, United Kingdom; Rossella Rota, Bambino Gesù Ospedale Pediatrico (IRCCS), Italy

                *Correspondence: Gianluca Campo cmpglc@ 123456unife.it

                This article was submitted to Clinical and Translational Physiology, a section of the journal Frontiers in Physiology

                Article
                10.3389/fphys.2018.00337
                5900783
                29686623
                3ffa980b-4b5e-452f-b999-48158e9de0a8
                Copyright © 2018 Vieceli Dalla Sega, Fortini, Aquila, Pavasini, Biscaglia, Bernucci, Del Franco, Tonet, Rizzo, Ferrari and Campo.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 08 February 2018
                : 19 March 2018
                Page count
                Figures: 6, Tables: 0, Equations: 0, References: 34, Pages: 8, Words: 4804
                Categories
                Physiology
                Original Research

                Anatomy & Physiology
                epidermal growth factor (egf),enos,ticagrelor,endothelial function,stable coronary artery disease (scad),chronic obstructive pulmonary disease (copd),egf

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