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Progressive study of effects of erianin on anticancer activity

Erianin is the major bisbenzyl compound extracted from the traditional Chinese medicine Dendrohium chrysotoxum Lindl. Erianin possesses many biological properties relevant to cancer prevention and therapy. The previous studies confirmed that antitumor effects of erianin are regulated with multiple s...

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Detalles Bibliográficos
Autores principales: Zhang, Yuying, Zhang, Qianqian, Wei, Fanhua, Liu, Na
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6628150/
https://www.ncbi.nlm.nih.gov/pubmed/31371985
http://dx.doi.org/10.2147/OTT.S200161
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author Zhang, Yuying
Zhang, Qianqian
Wei, Fanhua
Liu, Na
author_facet Zhang, Yuying
Zhang, Qianqian
Wei, Fanhua
Liu, Na
author_sort Zhang, Yuying
collection PubMed
description Erianin is the major bisbenzyl compound extracted from the traditional Chinese medicine Dendrohium chrysotoxum Lindl. Erianin possesses many biological properties relevant to cancer prevention and therapy. The previous studies confirmed that antitumor effects of erianin are regulated with multiple signaling pathways. The mechanisms of erianin are numerous, and most of them induce cancer cell apoptosis that may be intrinsic or extrinsic and modulate the ROS/JNK signaling pathways. Invasion, migration, and angiogenesis represent emerging targets of erianin and support its anticancer properties. This review aimed to summarize the recent advances in the antitumor activity of erianin and to provide a rationale for further exploring the potential application of erianin in overcoming cancer in the future.
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spelling pubmed-66281502019-08-01 Progressive study of effects of erianin on anticancer activity Zhang, Yuying Zhang, Qianqian Wei, Fanhua Liu, Na Onco Targets Ther Review Erianin is the major bisbenzyl compound extracted from the traditional Chinese medicine Dendrohium chrysotoxum Lindl. Erianin possesses many biological properties relevant to cancer prevention and therapy. The previous studies confirmed that antitumor effects of erianin are regulated with multiple signaling pathways. The mechanisms of erianin are numerous, and most of them induce cancer cell apoptosis that may be intrinsic or extrinsic and modulate the ROS/JNK signaling pathways. Invasion, migration, and angiogenesis represent emerging targets of erianin and support its anticancer properties. This review aimed to summarize the recent advances in the antitumor activity of erianin and to provide a rationale for further exploring the potential application of erianin in overcoming cancer in the future. Dove 2019-07-09 /pmc/articles/PMC6628150/ /pubmed/31371985 http://dx.doi.org/10.2147/OTT.S200161 Text en © 2019 Zhang et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Review
Zhang, Yuying
Zhang, Qianqian
Wei, Fanhua
Liu, Na
Progressive study of effects of erianin on anticancer activity
title Progressive study of effects of erianin on anticancer activity
title_full Progressive study of effects of erianin on anticancer activity
title_fullStr Progressive study of effects of erianin on anticancer activity
title_full_unstemmed Progressive study of effects of erianin on anticancer activity
title_short Progressive study of effects of erianin on anticancer activity
title_sort progressive study of effects of erianin on anticancer activity
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6628150/
https://www.ncbi.nlm.nih.gov/pubmed/31371985
http://dx.doi.org/10.2147/OTT.S200161
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