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      Natural Plants Compounds as Modulators of Epithelial-to-Mesenchymal Transition

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          Abstract

          Epithelial-to-mesenchymal transition (EMT) is a self-regulated physiological process required for tissue repair that, in non-controled conditions may lead to fibrosis, angiogenesis, loss of normal organ function or cancer. Although several molecular pathways involved in EMT regulation have been described, this process does not have any specific treatment. This article introduces a systematic review of effective natural plant compounds and their extract that modulates the pathological EMT or its deleterious effects, through acting on different cellular signal transduction pathways both in vivo and in vitro. Thereby, cryptotanshinone, resveratrol, oxymatrine, ligustrazine, osthole, codonolactone, betanin, tannic acid, gentiopicroside, curcumin, genistein, paeoniflorin, gambogic acid and Cinnamomum cassia extracts inhibit EMT acting on transforming growth factor-β (TGF-β)/Smads signaling pathways. Gedunin, carnosol, celastrol, black rice anthocyanins, Duchesnea indica, cordycepin and Celastrus orbiculatus extract downregulate vimectin, fibronectin and N-cadherin. Sulforaphane, luteolin, celastrol, curcumin, arctigenin inhibit β-catenin signaling pathways. Salvianolic acid-A and plumbagin block oxidative stress, while honokiol, gallic acid, piperlongumine, brusatol and paeoniflorin inhibit EMT transcription factors such as SNAIL, TWIST and ZEB. Plectranthoic acid, resveratrol, genistein, baicalin, polyphyllin I, cairicoside E, luteolin, berberine, nimbolide, curcumin, withaferin-A, jatrophone, ginsenoside-Rb1, honokiol, parthenolide, phoyunnanin-E, epicatechin-3-gallate, gigantol, eupatolide, baicalin and baicalein and nitidine chloride inhibit EMT acting on other signaling pathways (SIRT1, p38 MAPK, NFAT1, SMAD, IL-6, STAT3, AQP5, notch 1, PI3K/Akt, Wnt/β-catenin, NF-κB, FAK/AKT, Hh). Despite the huge amount of preclinical data regarding EMT modulation by the natural compounds of plant, clinical translation is poor. Additionally, this review highlights some relevant examples of clinical trials using natural plant compounds to modulate EMT and its deleterious effects. Overall, this opens up new therapeutic alternatives in cancer, inflammatory and fibrosing diseases through the control of EMT process.

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          Most cited references246

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          Epithelial-mesenchymal transitions in development and disease.

          The epithelial to mesenchymal transition (EMT) plays crucial roles in the formation of the body plan and in the differentiation of multiple tissues and organs. EMT also contributes to tissue repair, but it can adversely cause organ fibrosis and promote carcinoma progression through a variety of mechanisms. EMT endows cells with migratory and invasive properties, induces stem cell properties, prevents apoptosis and senescence, and contributes to immunosuppression. Thus, the mesenchymal state is associated with the capacity of cells to migrate to distant organs and maintain stemness, allowing their subsequent differentiation into multiple cell types during development and the initiation of metastasis.
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            • Article: not found

            How cells read TGF-beta signals.

            Cell proliferation, differentiation and death are controlled by a multitude of cell-cell signals, and loss of this control has devastating consequences. Prominent among these regulatory signals is the transforming growth factor-beta (TGF-beta) family of cytokines, which can trigger a bewildering diversity of responses, depending on the genetic makeup and environment of the target cell. What are the networks of cell-specific molecules that mould the TGF-beta response to each cell's needs?
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              Transcriptional control by the TGF-beta/Smad signaling system.

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                Author and article information

                Contributors
                URI : https://loop.frontiersin.org/people/516740
                URI : https://loop.frontiersin.org/people/738818
                URI : https://loop.frontiersin.org/people/521123
                URI : https://loop.frontiersin.org/people/180892
                URI : https://loop.frontiersin.org/people/632414
                Journal
                Front Pharmacol
                Front Pharmacol
                Front. Pharmacol.
                Frontiers in Pharmacology
                Frontiers Media S.A.
                1663-9812
                30 July 2019
                2019
                : 10
                : 715
                Affiliations
                [1] 1Therapeutic and Pharmacology Department, Health and Human Science Research, Academic Unit of Human Medicine and Health Sciences, Autonomous University of Zacatecas , Zacatecas, Mexico
                [2] 2Molecular Biology Unit, Research Institute of University Hospital La Princesa (IP) , Madrid, Spain
                [3] 3Department and Nephrology, Research Institute of University Hospital La Princesa (IP) , Madrid, Spain
                [4] 4Research Institute of La Paz (IdiPAZ), University Hospital La Paz , Madrid, Spain
                [5] 5Renal research network REDINREN , Madrid, Spain
                [6] 6Molecular Biology Research Centre Severo Ochoa, Spanish Council for Scientific Research (CSIC) , Madrid, Spain
                Author notes

                Edited by: Raffaele Strippoli, Sapienza University of Rome, Italy

                Reviewed by: Marco Cordani, IMDEA Nanociencia, Spain; Gautam Sethi, National University of Singapore, Singapore

                *Correspondence: Lorena Avila-Carrasco, lacdoc_@ 123456hotmail.com

                This article was submitted to Inflammation Pharmacology, a section of the journal Frontiers in Pharmacology

                †These authors have contributed equally to this work.

                ‡In memoriam.

                Article
                10.3389/fphar.2019.00715
                6682706
                31417401
                8dd8667f-b931-4628-ab82-b4800456da94
                Copyright © 2019 Avila-Carrasco, Majano, Sánchez-Toméro, Selgas, López-Cabrera, Aguilera and González Mateo

                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(s) 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
                : 10 March 2019
                : 05 June 2019
                Page count
                Figures: 1, Tables: 1, Equations: 0, References: 281, Pages: 24, Words: 10480
                Categories
                Pharmacology
                Review

                Pharmacology & Pharmaceutical medicine
                natural plants compounds,epithelial-to-mesenchymal transition (emt),anti-fibrotic,anti-inflammatory,anti-oxidant agent

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