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Taohong Siwu Decoction exerts anticancer effects on breast cancer via regulating MYC, BIRC5, EGF and PIK3R1 revealed by HTS(2) technology

Taohong Siwu Decoction (TSD), a classical gynecological prescription that was firstly reported 600 years ago, has been widely used in the adjuvant treatment of breast cancer (BRCA) in China. However, the mechanism of action of TSD in treating BRCA has remained unclear. Here, high-throughput sequenci...

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Autores principales: Gui, Yu, Dai, Yifei, Wang, Yumei, Li, Shengrong, Xiang, Lei, Tang, Yuqin, Tan, Xue, Pei, Tianli, Bao, Xilinqiqige, Wang, Dong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research Network of Computational and Structural Biotechnology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9278046/
https://www.ncbi.nlm.nih.gov/pubmed/35860405
http://dx.doi.org/10.1016/j.csbj.2022.06.044
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author Gui, Yu
Dai, Yifei
Wang, Yumei
Li, Shengrong
Xiang, Lei
Tang, Yuqin
Tan, Xue
Pei, Tianli
Bao, Xilinqiqige
Wang, Dong
author_facet Gui, Yu
Dai, Yifei
Wang, Yumei
Li, Shengrong
Xiang, Lei
Tang, Yuqin
Tan, Xue
Pei, Tianli
Bao, Xilinqiqige
Wang, Dong
author_sort Gui, Yu
collection PubMed
description Taohong Siwu Decoction (TSD), a classical gynecological prescription that was firstly reported 600 years ago, has been widely used in the adjuvant treatment of breast cancer (BRCA) in China. However, the mechanism of action of TSD in treating BRCA has remained unclear. Here, high-throughput sequencing-based high-throughput screening (HTS(2)) technology was used to reveal the molecular mechanism of TSD, combination with bioinformatics and systems pharmacology in this study. Firstly, our results showed that TSD exerts an anticancer effect on BRCA cells by inhibiting cell proliferation, migration and inducing apoptosis as well as cell-cycle arrest. And our results from HTS(2) suggested that herbs of TSD could significantly inhibit KRAS pathway and pathway in cancer, and activate apoptosis pathway, p53 pathway and hypoxia pathway, which may lead to the anticancer function of TSD. Further, we found that TSD clearly regulates MYC, BIRC5, EGF, and PIK3R1 genes, which play an important role in the development and progression of tumor and have significant correlation with overall survival in BRCA patients. By molecular docking, we discovered that Pentagalloylglucose, a compound derived from TSD, might directly bind to and inhibit the function of BRD4, which is a reported transcriptional activator of MYC gene, and thus repress the expression of MYC. Taken together, this study explores the mechanism of TSD in anti-BRCA by combining HTS(2) technology, bioinformatics analysis and systems pharmacology.
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spelling pubmed-92780462022-07-19 Taohong Siwu Decoction exerts anticancer effects on breast cancer via regulating MYC, BIRC5, EGF and PIK3R1 revealed by HTS(2) technology Gui, Yu Dai, Yifei Wang, Yumei Li, Shengrong Xiang, Lei Tang, Yuqin Tan, Xue Pei, Tianli Bao, Xilinqiqige Wang, Dong Comput Struct Biotechnol J Research Article Taohong Siwu Decoction (TSD), a classical gynecological prescription that was firstly reported 600 years ago, has been widely used in the adjuvant treatment of breast cancer (BRCA) in China. However, the mechanism of action of TSD in treating BRCA has remained unclear. Here, high-throughput sequencing-based high-throughput screening (HTS(2)) technology was used to reveal the molecular mechanism of TSD, combination with bioinformatics and systems pharmacology in this study. Firstly, our results showed that TSD exerts an anticancer effect on BRCA cells by inhibiting cell proliferation, migration and inducing apoptosis as well as cell-cycle arrest. And our results from HTS(2) suggested that herbs of TSD could significantly inhibit KRAS pathway and pathway in cancer, and activate apoptosis pathway, p53 pathway and hypoxia pathway, which may lead to the anticancer function of TSD. Further, we found that TSD clearly regulates MYC, BIRC5, EGF, and PIK3R1 genes, which play an important role in the development and progression of tumor and have significant correlation with overall survival in BRCA patients. By molecular docking, we discovered that Pentagalloylglucose, a compound derived from TSD, might directly bind to and inhibit the function of BRD4, which is a reported transcriptional activator of MYC gene, and thus repress the expression of MYC. Taken together, this study explores the mechanism of TSD in anti-BRCA by combining HTS(2) technology, bioinformatics analysis and systems pharmacology. Research Network of Computational and Structural Biotechnology 2022-06-26 /pmc/articles/PMC9278046/ /pubmed/35860405 http://dx.doi.org/10.1016/j.csbj.2022.06.044 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Gui, Yu
Dai, Yifei
Wang, Yumei
Li, Shengrong
Xiang, Lei
Tang, Yuqin
Tan, Xue
Pei, Tianli
Bao, Xilinqiqige
Wang, Dong
Taohong Siwu Decoction exerts anticancer effects on breast cancer via regulating MYC, BIRC5, EGF and PIK3R1 revealed by HTS(2) technology
title Taohong Siwu Decoction exerts anticancer effects on breast cancer via regulating MYC, BIRC5, EGF and PIK3R1 revealed by HTS(2) technology
title_full Taohong Siwu Decoction exerts anticancer effects on breast cancer via regulating MYC, BIRC5, EGF and PIK3R1 revealed by HTS(2) technology
title_fullStr Taohong Siwu Decoction exerts anticancer effects on breast cancer via regulating MYC, BIRC5, EGF and PIK3R1 revealed by HTS(2) technology
title_full_unstemmed Taohong Siwu Decoction exerts anticancer effects on breast cancer via regulating MYC, BIRC5, EGF and PIK3R1 revealed by HTS(2) technology
title_short Taohong Siwu Decoction exerts anticancer effects on breast cancer via regulating MYC, BIRC5, EGF and PIK3R1 revealed by HTS(2) technology
title_sort taohong siwu decoction exerts anticancer effects on breast cancer via regulating myc, birc5, egf and pik3r1 revealed by hts(2) technology
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9278046/
https://www.ncbi.nlm.nih.gov/pubmed/35860405
http://dx.doi.org/10.1016/j.csbj.2022.06.044
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