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

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 desc...

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Autores principales: Avila-Carrasco, Lorena, Majano, Pedro, Sánchez-Toméro, José Antonio, Selgas, Rafael, López-Cabrera, Manuel, Aguilera, Abelardo, González Mateo, Guadalupe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6682706/
https://www.ncbi.nlm.nih.gov/pubmed/31417401
http://dx.doi.org/10.3389/fphar.2019.00715
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author Avila-Carrasco, Lorena
Majano, Pedro
Sánchez-Toméro, José Antonio
Selgas, Rafael
López-Cabrera, Manuel
Aguilera, Abelardo
González Mateo, Guadalupe
author_facet Avila-Carrasco, Lorena
Majano, Pedro
Sánchez-Toméro, José Antonio
Selgas, Rafael
López-Cabrera, Manuel
Aguilera, Abelardo
González Mateo, Guadalupe
author_sort Avila-Carrasco, Lorena
collection PubMed
description 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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spelling pubmed-66827062019-08-15 Natural Plants Compounds as Modulators of Epithelial-to-Mesenchymal Transition Avila-Carrasco, Lorena Majano, Pedro Sánchez-Toméro, José Antonio Selgas, Rafael López-Cabrera, Manuel Aguilera, Abelardo González Mateo, Guadalupe Front Pharmacol Pharmacology 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. Frontiers Media S.A. 2019-07-30 /pmc/articles/PMC6682706/ /pubmed/31417401 http://dx.doi.org/10.3389/fphar.2019.00715 Text en Copyright © 2019 Avila-Carrasco, Majano, Sánchez-Toméro, Selgas, López-Cabrera, Aguilera and González Mateo http://creativecommons.org/licenses/by/4.0/ 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.
spellingShingle Pharmacology
Avila-Carrasco, Lorena
Majano, Pedro
Sánchez-Toméro, José Antonio
Selgas, Rafael
López-Cabrera, Manuel
Aguilera, Abelardo
González Mateo, Guadalupe
Natural Plants Compounds as Modulators of Epithelial-to-Mesenchymal Transition
title Natural Plants Compounds as Modulators of Epithelial-to-Mesenchymal Transition
title_full Natural Plants Compounds as Modulators of Epithelial-to-Mesenchymal Transition
title_fullStr Natural Plants Compounds as Modulators of Epithelial-to-Mesenchymal Transition
title_full_unstemmed Natural Plants Compounds as Modulators of Epithelial-to-Mesenchymal Transition
title_short Natural Plants Compounds as Modulators of Epithelial-to-Mesenchymal Transition
title_sort natural plants compounds as modulators of epithelial-to-mesenchymal transition
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6682706/
https://www.ncbi.nlm.nih.gov/pubmed/31417401
http://dx.doi.org/10.3389/fphar.2019.00715
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