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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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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. |
format | Online Article Text |
id | pubmed-6682706 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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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