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The effect of compound kushen injection on cancer cells: Integrated identification of candidate molecular mechanisms

Traditional Chinese Medicine (TCM) preparations are often extracts of single or multiple herbs containing hundreds of compounds, and hence it has been difficult to study their mechanisms of action. Compound Kushen Injection (CKI) is a complex mixture of compounds extracted from two medicinal plants...

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Autores principales: Cui, Jian, Qu, Zhipeng, Harata-Lee, Yuka, Shen, Hanyuan, Aung, Thazin Nwe, Wang, Wei, Kortschak, R. Daniel, Adelson, David L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7392229/
https://www.ncbi.nlm.nih.gov/pubmed/32730293
http://dx.doi.org/10.1371/journal.pone.0236395
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author Cui, Jian
Qu, Zhipeng
Harata-Lee, Yuka
Shen, Hanyuan
Aung, Thazin Nwe
Wang, Wei
Kortschak, R. Daniel
Adelson, David L.
author_facet Cui, Jian
Qu, Zhipeng
Harata-Lee, Yuka
Shen, Hanyuan
Aung, Thazin Nwe
Wang, Wei
Kortschak, R. Daniel
Adelson, David L.
author_sort Cui, Jian
collection PubMed
description Traditional Chinese Medicine (TCM) preparations are often extracts of single or multiple herbs containing hundreds of compounds, and hence it has been difficult to study their mechanisms of action. Compound Kushen Injection (CKI) is a complex mixture of compounds extracted from two medicinal plants and has been used in Chinese hospitals to treat cancer for over twenty years. To demonstrate that a systematic analysis of molecular changes resulting from complex mixtures of bioactives from TCM can identify a core set of differentially expressed (DE) genes and a reproducible set of candidate pathways. We used in vitro cancer models to measure the effect of CKI on cell cycle phases and apoptosis, and correlated those phenotypes with CKI induced changes in gene expression. We treated two cancer cell lines with or without CKI and assessed the resulting phenotypes by employing cell viability and proliferation assays. Based on these results, we carried out high-throughput transcriptome data analysis to identify genes and candidate pathways perturbed by CKI. We integrated these differential gene expression results with previously reported results and carried out validation of selected differentially expressed genes. CKI induced cell-cycle arrest and apoptosis in the cancer cell lines tested. In these cells CKI also altered the expression of 363 core candidate genes associated with cell cycle, apoptosis, DNA replication/repair, and various cancer pathways. Of these, 7 are clinically relevant to cancer diagnosis or therapy, 14 are cell cycle regulators, and most of these 21 candidates are downregulated by CKI. Comparison of our core candidate genes to a database of plant medicinal compounds and their effects on gene expression identified one-to-one, one-to-many and many-to-many regulatory relationships between compounds in CKI and DE genes. By identifying genes and promising candidate pathways associated with CKI treatment based on our transcriptome-based analysis, we have shown that this approach is useful for the systematic analysis of molecular changes resulting from complex mixtures of bioactives.
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spelling pubmed-73922292020-08-05 The effect of compound kushen injection on cancer cells: Integrated identification of candidate molecular mechanisms Cui, Jian Qu, Zhipeng Harata-Lee, Yuka Shen, Hanyuan Aung, Thazin Nwe Wang, Wei Kortschak, R. Daniel Adelson, David L. PLoS One Research Article Traditional Chinese Medicine (TCM) preparations are often extracts of single or multiple herbs containing hundreds of compounds, and hence it has been difficult to study their mechanisms of action. Compound Kushen Injection (CKI) is a complex mixture of compounds extracted from two medicinal plants and has been used in Chinese hospitals to treat cancer for over twenty years. To demonstrate that a systematic analysis of molecular changes resulting from complex mixtures of bioactives from TCM can identify a core set of differentially expressed (DE) genes and a reproducible set of candidate pathways. We used in vitro cancer models to measure the effect of CKI on cell cycle phases and apoptosis, and correlated those phenotypes with CKI induced changes in gene expression. We treated two cancer cell lines with or without CKI and assessed the resulting phenotypes by employing cell viability and proliferation assays. Based on these results, we carried out high-throughput transcriptome data analysis to identify genes and candidate pathways perturbed by CKI. We integrated these differential gene expression results with previously reported results and carried out validation of selected differentially expressed genes. CKI induced cell-cycle arrest and apoptosis in the cancer cell lines tested. In these cells CKI also altered the expression of 363 core candidate genes associated with cell cycle, apoptosis, DNA replication/repair, and various cancer pathways. Of these, 7 are clinically relevant to cancer diagnosis or therapy, 14 are cell cycle regulators, and most of these 21 candidates are downregulated by CKI. Comparison of our core candidate genes to a database of plant medicinal compounds and their effects on gene expression identified one-to-one, one-to-many and many-to-many regulatory relationships between compounds in CKI and DE genes. By identifying genes and promising candidate pathways associated with CKI treatment based on our transcriptome-based analysis, we have shown that this approach is useful for the systematic analysis of molecular changes resulting from complex mixtures of bioactives. Public Library of Science 2020-07-30 /pmc/articles/PMC7392229/ /pubmed/32730293 http://dx.doi.org/10.1371/journal.pone.0236395 Text en © 2020 Cui et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Cui, Jian
Qu, Zhipeng
Harata-Lee, Yuka
Shen, Hanyuan
Aung, Thazin Nwe
Wang, Wei
Kortschak, R. Daniel
Adelson, David L.
The effect of compound kushen injection on cancer cells: Integrated identification of candidate molecular mechanisms
title The effect of compound kushen injection on cancer cells: Integrated identification of candidate molecular mechanisms
title_full The effect of compound kushen injection on cancer cells: Integrated identification of candidate molecular mechanisms
title_fullStr The effect of compound kushen injection on cancer cells: Integrated identification of candidate molecular mechanisms
title_full_unstemmed The effect of compound kushen injection on cancer cells: Integrated identification of candidate molecular mechanisms
title_short The effect of compound kushen injection on cancer cells: Integrated identification of candidate molecular mechanisms
title_sort effect of compound kushen injection on cancer cells: integrated identification of candidate molecular mechanisms
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7392229/
https://www.ncbi.nlm.nih.gov/pubmed/32730293
http://dx.doi.org/10.1371/journal.pone.0236395
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