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Inhibitory Effects of Ginsenoside Ro on the Growth of B16F10 Melanoma via Its Metabolites
Ginsenoside Ro (Ro), a major saponin derived and isolated from Panax ginseng C.A. Meyer, exerts multiple biological activities. However, the anti-tumour efficacy of Ro remains unclear because of its poor in vitro effects. In this study, we confirmed that Ro has no anti-tumour activity in vitro. We e...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6721120/ https://www.ncbi.nlm.nih.gov/pubmed/31426477 http://dx.doi.org/10.3390/molecules24162985 |
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author | Zheng, Si-wen Xiao, Sheng-yuan Wang, Jia Hou, Wei Wang, Ying-ping |
author_facet | Zheng, Si-wen Xiao, Sheng-yuan Wang, Jia Hou, Wei Wang, Ying-ping |
author_sort | Zheng, Si-wen |
collection | PubMed |
description | Ginsenoside Ro (Ro), a major saponin derived and isolated from Panax ginseng C.A. Meyer, exerts multiple biological activities. However, the anti-tumour efficacy of Ro remains unclear because of its poor in vitro effects. In this study, we confirmed that Ro has no anti-tumour activity in vitro. We explored the anti-tumour activity of Ro in vivo in B16F10 tumour-bearing mice. The results revealed that Ro considerably suppressed tumour growth with no significant side effects on immune organs and body weight. Zingibroside R1, chikusetsusaponin IVa, and calenduloside E, three metabolites of Ro, were detected in the plasma of Ro-treated tumour-bearing mice and showed excellent anti-tumour effects as well as anti-angiogenic activity. The results suggest that the metabolites play important roles in the anti-tumour efficacy of Ro in vivo. Additionally, the haemolysis test demonstrated that Ro has good biocompatibility. Taken together, the findings of this study demonstrate that Ro markedly suppresses the tumour growth of B16F10-transplanted tumours in vivo, and its anti-tumour effects are based on the biological activity of its metabolites. The anti-tumour efficacy of these metabolites is due, at least in part, to its anti-angiogenic activity. |
format | Online Article Text |
id | pubmed-6721120 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-67211202019-09-10 Inhibitory Effects of Ginsenoside Ro on the Growth of B16F10 Melanoma via Its Metabolites Zheng, Si-wen Xiao, Sheng-yuan Wang, Jia Hou, Wei Wang, Ying-ping Molecules Article Ginsenoside Ro (Ro), a major saponin derived and isolated from Panax ginseng C.A. Meyer, exerts multiple biological activities. However, the anti-tumour efficacy of Ro remains unclear because of its poor in vitro effects. In this study, we confirmed that Ro has no anti-tumour activity in vitro. We explored the anti-tumour activity of Ro in vivo in B16F10 tumour-bearing mice. The results revealed that Ro considerably suppressed tumour growth with no significant side effects on immune organs and body weight. Zingibroside R1, chikusetsusaponin IVa, and calenduloside E, three metabolites of Ro, were detected in the plasma of Ro-treated tumour-bearing mice and showed excellent anti-tumour effects as well as anti-angiogenic activity. The results suggest that the metabolites play important roles in the anti-tumour efficacy of Ro in vivo. Additionally, the haemolysis test demonstrated that Ro has good biocompatibility. Taken together, the findings of this study demonstrate that Ro markedly suppresses the tumour growth of B16F10-transplanted tumours in vivo, and its anti-tumour effects are based on the biological activity of its metabolites. The anti-tumour efficacy of these metabolites is due, at least in part, to its anti-angiogenic activity. MDPI 2019-08-17 /pmc/articles/PMC6721120/ /pubmed/31426477 http://dx.doi.org/10.3390/molecules24162985 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Zheng, Si-wen Xiao, Sheng-yuan Wang, Jia Hou, Wei Wang, Ying-ping Inhibitory Effects of Ginsenoside Ro on the Growth of B16F10 Melanoma via Its Metabolites |
title | Inhibitory Effects of Ginsenoside Ro on the Growth of B16F10 Melanoma via Its Metabolites |
title_full | Inhibitory Effects of Ginsenoside Ro on the Growth of B16F10 Melanoma via Its Metabolites |
title_fullStr | Inhibitory Effects of Ginsenoside Ro on the Growth of B16F10 Melanoma via Its Metabolites |
title_full_unstemmed | Inhibitory Effects of Ginsenoside Ro on the Growth of B16F10 Melanoma via Its Metabolites |
title_short | Inhibitory Effects of Ginsenoside Ro on the Growth of B16F10 Melanoma via Its Metabolites |
title_sort | inhibitory effects of ginsenoside ro on the growth of b16f10 melanoma via its metabolites |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6721120/ https://www.ncbi.nlm.nih.gov/pubmed/31426477 http://dx.doi.org/10.3390/molecules24162985 |
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