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Saikosaponin D: review on the antitumour effects, toxicity and pharmacokinetics

CONTEXT: Bupleuri Radix, the dried root of Bupleurum chinense DC and Bupleurum scorzonerifolium Willd (Apiaceae), is an important medicinal herb widely used to treat cancers for hundreds of years in Asian countries. As the most antitumour component but also the main toxic component in Bupleuri Radix...

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Autores principales: Zhou, Piao, Shi, Wei, He, Xiao-Yan, Du, Quan-Yu, Wang, Fei, Guo, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8567945/
https://www.ncbi.nlm.nih.gov/pubmed/34714209
http://dx.doi.org/10.1080/13880209.2021.1992448
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author Zhou, Piao
Shi, Wei
He, Xiao-Yan
Du, Quan-Yu
Wang, Fei
Guo, Jing
author_facet Zhou, Piao
Shi, Wei
He, Xiao-Yan
Du, Quan-Yu
Wang, Fei
Guo, Jing
author_sort Zhou, Piao
collection PubMed
description CONTEXT: Bupleuri Radix, the dried root of Bupleurum chinense DC and Bupleurum scorzonerifolium Willd (Apiaceae), is an important medicinal herb widely used to treat cancers for hundreds of years in Asian countries. As the most antitumour component but also the main toxic component in Bupleuri Radix, saikosaponin D (SSD) has attracted extensive attention. However, no summary studies have been reported on the antitumour effects, toxicity and pharmacokinetics of this potential natural anticancer substance. OBJECTIVE: To analyse and summarise the existing findings regarding to the antitumour effects, toxicity and pharmacokinetics of SSD. MATERIALS AND METHODS: We collected relevant information published before April 2021 by conducting a search of literature available in various online databases including PubMed, Science Direct, CNKI, Wanfang database and the Chinese Biological Medicine Database. Bupleurum, Bupleuri Radix, saikosaponin, saikosaponin D, tumour, toxicity, and pharmacokinetics were used as the keywords. RESULTS: The antitumour effects of SSD were multi-targeted and can be realised through various mechanisms, including inhibition of proliferation, invasion, metastasis and angiogenesis, as well as induction of cell apoptosis, autophagy, and differentiation. The toxicological effects of SSD mainly included hepatotoxicity, neurotoxicity, haemolysis and cardiotoxicity. Pharmacokinetic studies demonstrated that SSD had the potential to alter the pharmacokinetics of some drugs for its influence on CYPs and P-gp, and the oral bioavailability and actual pharmacodynamic substances in vivo of SSD are still controversial. CONCLUSIONS: SSD is a potentially effective and relatively safe natural antitumour substance, but more research is needed, especially in vivo antitumour effects and pharmacokinetics of the compound.
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spelling pubmed-85679452021-11-05 Saikosaponin D: review on the antitumour effects, toxicity and pharmacokinetics Zhou, Piao Shi, Wei He, Xiao-Yan Du, Quan-Yu Wang, Fei Guo, Jing Pharm Biol Review Article CONTEXT: Bupleuri Radix, the dried root of Bupleurum chinense DC and Bupleurum scorzonerifolium Willd (Apiaceae), is an important medicinal herb widely used to treat cancers for hundreds of years in Asian countries. As the most antitumour component but also the main toxic component in Bupleuri Radix, saikosaponin D (SSD) has attracted extensive attention. However, no summary studies have been reported on the antitumour effects, toxicity and pharmacokinetics of this potential natural anticancer substance. OBJECTIVE: To analyse and summarise the existing findings regarding to the antitumour effects, toxicity and pharmacokinetics of SSD. MATERIALS AND METHODS: We collected relevant information published before April 2021 by conducting a search of literature available in various online databases including PubMed, Science Direct, CNKI, Wanfang database and the Chinese Biological Medicine Database. Bupleurum, Bupleuri Radix, saikosaponin, saikosaponin D, tumour, toxicity, and pharmacokinetics were used as the keywords. RESULTS: The antitumour effects of SSD were multi-targeted and can be realised through various mechanisms, including inhibition of proliferation, invasion, metastasis and angiogenesis, as well as induction of cell apoptosis, autophagy, and differentiation. The toxicological effects of SSD mainly included hepatotoxicity, neurotoxicity, haemolysis and cardiotoxicity. Pharmacokinetic studies demonstrated that SSD had the potential to alter the pharmacokinetics of some drugs for its influence on CYPs and P-gp, and the oral bioavailability and actual pharmacodynamic substances in vivo of SSD are still controversial. CONCLUSIONS: SSD is a potentially effective and relatively safe natural antitumour substance, but more research is needed, especially in vivo antitumour effects and pharmacokinetics of the compound. Taylor & Francis 2021-10-29 /pmc/articles/PMC8567945/ /pubmed/34714209 http://dx.doi.org/10.1080/13880209.2021.1992448 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Zhou, Piao
Shi, Wei
He, Xiao-Yan
Du, Quan-Yu
Wang, Fei
Guo, Jing
Saikosaponin D: review on the antitumour effects, toxicity and pharmacokinetics
title Saikosaponin D: review on the antitumour effects, toxicity and pharmacokinetics
title_full Saikosaponin D: review on the antitumour effects, toxicity and pharmacokinetics
title_fullStr Saikosaponin D: review on the antitumour effects, toxicity and pharmacokinetics
title_full_unstemmed Saikosaponin D: review on the antitumour effects, toxicity and pharmacokinetics
title_short Saikosaponin D: review on the antitumour effects, toxicity and pharmacokinetics
title_sort saikosaponin d: review on the antitumour effects, toxicity and pharmacokinetics
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8567945/
https://www.ncbi.nlm.nih.gov/pubmed/34714209
http://dx.doi.org/10.1080/13880209.2021.1992448
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