Cargando…

The Pharmacological Mechanisms of Xiaochaihutang in Treating Breast Cancer Based on Network Pharmacology

BACKGROUND: As a classic prescription in Chinese medicine treatment, Xiaochaihutang (XCHT) can improve the clinical effect and reduce serum tumor markers in patients with breast cancer (BC). However, there has not been any study to confirm the mechanism. We used bioinformatics analysis and network p...

Descripción completa

Detalles Bibliográficos
Autores principales: Zheng, Lin, Jiang, Hongnan, Li, Ruoqi, Song, Liying, Chen, Ruihan, Dong, Honglin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8926522/
https://www.ncbi.nlm.nih.gov/pubmed/35350700
http://dx.doi.org/10.1155/2022/3900636
_version_ 1784670255603253248
author Zheng, Lin
Jiang, Hongnan
Li, Ruoqi
Song, Liying
Chen, Ruihan
Dong, Honglin
author_facet Zheng, Lin
Jiang, Hongnan
Li, Ruoqi
Song, Liying
Chen, Ruihan
Dong, Honglin
author_sort Zheng, Lin
collection PubMed
description BACKGROUND: As a classic prescription in Chinese medicine treatment, Xiaochaihutang (XCHT) can improve the clinical effect and reduce serum tumor markers in patients with breast cancer (BC). However, there has not been any study to confirm the mechanism. We used bioinformatics analysis and network pharmacology to find the potential targets. METHODS: The differentially expressed genes (DEGs) of BC were identified from the Cancer Genome Atlas (TCGA) dataset. Then, we utilized weighted coexpression network analysis (WGCNA) with the same dataset. The target genes of BC were obtained by comparing genes of DEGs and in significant modules of WGCNA. Drug targets of XCHT from the Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform (TCMSP) database were intersected with the targets of BC. The protein-protein interaction (PPI) of the drug targets was analysed by using the STRING database. We utilized the Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes analysis (KEGG) enrichment analysis to identify the specific pathways and key target proteins. Receiver operator characteristic (ROC) curve was used as the verification of drug targets. Molecular docking was performed to visualize the patterns of interactions between the effective molecule and targeted protein. RESULTS: We obtained a set of 21 target genes, which mainly encode neurotransmitter receptors or related transporters, such as OPRD1, 5-HT2A, and so on. In addition, enrichment analyses of 21 target genes showed that they were mainly concentrated in pathways related to the nervous system. Molecular docking was performed on the target gene of BC. Six active compounds can enter the active pocket of target gene, namely, naringenin, beta-sitosterol, coumestrol, nuciferine, beta-sitosterol, and protopine, thereby exerting potential therapeutic effects in BC. CONCLUSIONS: Our analysis shows that the mechanism of XCHT in the treatment of BC is mainly acting on the neurogenesis in the microenvironment of breast tumor tissue.
format Online
Article
Text
id pubmed-8926522
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Hindawi
record_format MEDLINE/PubMed
spelling pubmed-89265222022-03-28 The Pharmacological Mechanisms of Xiaochaihutang in Treating Breast Cancer Based on Network Pharmacology Zheng, Lin Jiang, Hongnan Li, Ruoqi Song, Liying Chen, Ruihan Dong, Honglin Contrast Media Mol Imaging Research Article BACKGROUND: As a classic prescription in Chinese medicine treatment, Xiaochaihutang (XCHT) can improve the clinical effect and reduce serum tumor markers in patients with breast cancer (BC). However, there has not been any study to confirm the mechanism. We used bioinformatics analysis and network pharmacology to find the potential targets. METHODS: The differentially expressed genes (DEGs) of BC were identified from the Cancer Genome Atlas (TCGA) dataset. Then, we utilized weighted coexpression network analysis (WGCNA) with the same dataset. The target genes of BC were obtained by comparing genes of DEGs and in significant modules of WGCNA. Drug targets of XCHT from the Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform (TCMSP) database were intersected with the targets of BC. The protein-protein interaction (PPI) of the drug targets was analysed by using the STRING database. We utilized the Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes analysis (KEGG) enrichment analysis to identify the specific pathways and key target proteins. Receiver operator characteristic (ROC) curve was used as the verification of drug targets. Molecular docking was performed to visualize the patterns of interactions between the effective molecule and targeted protein. RESULTS: We obtained a set of 21 target genes, which mainly encode neurotransmitter receptors or related transporters, such as OPRD1, 5-HT2A, and so on. In addition, enrichment analyses of 21 target genes showed that they were mainly concentrated in pathways related to the nervous system. Molecular docking was performed on the target gene of BC. Six active compounds can enter the active pocket of target gene, namely, naringenin, beta-sitosterol, coumestrol, nuciferine, beta-sitosterol, and protopine, thereby exerting potential therapeutic effects in BC. CONCLUSIONS: Our analysis shows that the mechanism of XCHT in the treatment of BC is mainly acting on the neurogenesis in the microenvironment of breast tumor tissue. Hindawi 2022-03-09 /pmc/articles/PMC8926522/ /pubmed/35350700 http://dx.doi.org/10.1155/2022/3900636 Text en Copyright © 2022 Lin Zheng et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zheng, Lin
Jiang, Hongnan
Li, Ruoqi
Song, Liying
Chen, Ruihan
Dong, Honglin
The Pharmacological Mechanisms of Xiaochaihutang in Treating Breast Cancer Based on Network Pharmacology
title The Pharmacological Mechanisms of Xiaochaihutang in Treating Breast Cancer Based on Network Pharmacology
title_full The Pharmacological Mechanisms of Xiaochaihutang in Treating Breast Cancer Based on Network Pharmacology
title_fullStr The Pharmacological Mechanisms of Xiaochaihutang in Treating Breast Cancer Based on Network Pharmacology
title_full_unstemmed The Pharmacological Mechanisms of Xiaochaihutang in Treating Breast Cancer Based on Network Pharmacology
title_short The Pharmacological Mechanisms of Xiaochaihutang in Treating Breast Cancer Based on Network Pharmacology
title_sort pharmacological mechanisms of xiaochaihutang in treating breast cancer based on network pharmacology
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8926522/
https://www.ncbi.nlm.nih.gov/pubmed/35350700
http://dx.doi.org/10.1155/2022/3900636
work_keys_str_mv AT zhenglin thepharmacologicalmechanismsofxiaochaihutangintreatingbreastcancerbasedonnetworkpharmacology
AT jianghongnan thepharmacologicalmechanismsofxiaochaihutangintreatingbreastcancerbasedonnetworkpharmacology
AT liruoqi thepharmacologicalmechanismsofxiaochaihutangintreatingbreastcancerbasedonnetworkpharmacology
AT songliying thepharmacologicalmechanismsofxiaochaihutangintreatingbreastcancerbasedonnetworkpharmacology
AT chenruihan thepharmacologicalmechanismsofxiaochaihutangintreatingbreastcancerbasedonnetworkpharmacology
AT donghonglin thepharmacologicalmechanismsofxiaochaihutangintreatingbreastcancerbasedonnetworkpharmacology
AT zhenglin pharmacologicalmechanismsofxiaochaihutangintreatingbreastcancerbasedonnetworkpharmacology
AT jianghongnan pharmacologicalmechanismsofxiaochaihutangintreatingbreastcancerbasedonnetworkpharmacology
AT liruoqi pharmacologicalmechanismsofxiaochaihutangintreatingbreastcancerbasedonnetworkpharmacology
AT songliying pharmacologicalmechanismsofxiaochaihutangintreatingbreastcancerbasedonnetworkpharmacology
AT chenruihan pharmacologicalmechanismsofxiaochaihutangintreatingbreastcancerbasedonnetworkpharmacology
AT donghonglin pharmacologicalmechanismsofxiaochaihutangintreatingbreastcancerbasedonnetworkpharmacology