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Screening the active compounds of Phellodendri Amurensis cortex for treating prostate cancer by high-throughput chinmedomics
Screening the active compounds of herbal medicines is of importance to modern drug discovery. In this work, an integrative strategy was established to discover the effective compounds and their therapeutic targets using Phellodendri Amurensis cortex (PAC) aimed at inhibiting prostate cancer as a cas...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5382783/ https://www.ncbi.nlm.nih.gov/pubmed/28383015 http://dx.doi.org/10.1038/srep46234 |
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author | Li, Xian-Na Zhang, Aihua Wang, Meijia Sun, Hui Liu, Zhidong Qiu, Shi Zhang, Tianlei Wang, Xijun |
author_facet | Li, Xian-Na Zhang, Aihua Wang, Meijia Sun, Hui Liu, Zhidong Qiu, Shi Zhang, Tianlei Wang, Xijun |
author_sort | Li, Xian-Na |
collection | PubMed |
description | Screening the active compounds of herbal medicines is of importance to modern drug discovery. In this work, an integrative strategy was established to discover the effective compounds and their therapeutic targets using Phellodendri Amurensis cortex (PAC) aimed at inhibiting prostate cancer as a case study. We found that PAC could be inhibited the growth of xenograft tumours of prostate cancer. Global constituents and serum metabolites were analysed by UPLC-MS based on the established chinmedomics analysis method, a total of 54 peaks in the spectrum of PAC were characterised in vitro and 38 peaks were characterised in vivo. Among the 38 compounds characterised in vivo, 29 prototype components were absorbed in serum and nine metabolites were identified in vivo. Thirty-four metabolic biomarkers were related to prostate cancer, and PAC could observably reverse these metabolic biomarkers to their normal level and regulate the disturbed metabolic profile to a healthy state. A chinmedomics approach showed that ten absorbed constituents, as effective compounds, were associated with the therapeutic effect of PAC. In combination with bioactivity assays, the action targets were also predicted and discovered. As an illustrative case study, the strategy was successfully applied to high-throughput screening of active compounds from herbal medicine. |
format | Online Article Text |
id | pubmed-5382783 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53827832017-04-11 Screening the active compounds of Phellodendri Amurensis cortex for treating prostate cancer by high-throughput chinmedomics Li, Xian-Na Zhang, Aihua Wang, Meijia Sun, Hui Liu, Zhidong Qiu, Shi Zhang, Tianlei Wang, Xijun Sci Rep Article Screening the active compounds of herbal medicines is of importance to modern drug discovery. In this work, an integrative strategy was established to discover the effective compounds and their therapeutic targets using Phellodendri Amurensis cortex (PAC) aimed at inhibiting prostate cancer as a case study. We found that PAC could be inhibited the growth of xenograft tumours of prostate cancer. Global constituents and serum metabolites were analysed by UPLC-MS based on the established chinmedomics analysis method, a total of 54 peaks in the spectrum of PAC were characterised in vitro and 38 peaks were characterised in vivo. Among the 38 compounds characterised in vivo, 29 prototype components were absorbed in serum and nine metabolites were identified in vivo. Thirty-four metabolic biomarkers were related to prostate cancer, and PAC could observably reverse these metabolic biomarkers to their normal level and regulate the disturbed metabolic profile to a healthy state. A chinmedomics approach showed that ten absorbed constituents, as effective compounds, were associated with the therapeutic effect of PAC. In combination with bioactivity assays, the action targets were also predicted and discovered. As an illustrative case study, the strategy was successfully applied to high-throughput screening of active compounds from herbal medicine. Nature Publishing Group 2017-04-06 /pmc/articles/PMC5382783/ /pubmed/28383015 http://dx.doi.org/10.1038/srep46234 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Li, Xian-Na Zhang, Aihua Wang, Meijia Sun, Hui Liu, Zhidong Qiu, Shi Zhang, Tianlei Wang, Xijun Screening the active compounds of Phellodendri Amurensis cortex for treating prostate cancer by high-throughput chinmedomics |
title | Screening the active compounds of Phellodendri Amurensis cortex for treating prostate cancer by high-throughput chinmedomics |
title_full | Screening the active compounds of Phellodendri Amurensis cortex for treating prostate cancer by high-throughput chinmedomics |
title_fullStr | Screening the active compounds of Phellodendri Amurensis cortex for treating prostate cancer by high-throughput chinmedomics |
title_full_unstemmed | Screening the active compounds of Phellodendri Amurensis cortex for treating prostate cancer by high-throughput chinmedomics |
title_short | Screening the active compounds of Phellodendri Amurensis cortex for treating prostate cancer by high-throughput chinmedomics |
title_sort | screening the active compounds of phellodendri amurensis cortex for treating prostate cancer by high-throughput chinmedomics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5382783/ https://www.ncbi.nlm.nih.gov/pubmed/28383015 http://dx.doi.org/10.1038/srep46234 |
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