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Research into the mechanism of intervention of SanQi in endometriosis based on network pharmacology and molecular docking technology
By using network pharmacology and molecular docking technology, we have explored the mechanism of action of Sanqi in the treatment of endometriosis (EMS), in order to provide reference for clinical studies of Chinese medicine treatment of Ems and Chinese medicine pharmacology. METHODS: There are 123...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9478308/ https://www.ncbi.nlm.nih.gov/pubmed/36123943 http://dx.doi.org/10.1097/MD.0000000000030021 |
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author | Lin, Zhiheng Fan, Weisen Yu, Xiao Liu, Jinxing Liu, Pengfei |
author_facet | Lin, Zhiheng Fan, Weisen Yu, Xiao Liu, Jinxing Liu, Pengfei |
author_sort | Lin, Zhiheng |
collection | PubMed |
description | By using network pharmacology and molecular docking technology, we have explored the mechanism of action of Sanqi in the treatment of endometriosis (EMS), in order to provide reference for clinical studies of Chinese medicine treatment of Ems and Chinese medicine pharmacology. METHODS: There are 123 intersecting targets between the active ingredients of Sanqi and disease targets. In the Protein-Protein Interaction network, Jun proto-oncogene, AP-1 transcription factor subunit, tumor necrosis factor, interleukin 6, etc., are the core proteins. The top 20 genes ranked by degree have been analyzed according to the Kyoto Encyclopedia of Genes and Genomes pathway and Gene Ontology analysis, and 20 pathways have been identified. RESULTS: On the Kyoto Encyclopedia of Genes and Genomes pathway, the most important part is the phosphatidylinositol 3’-kinase-Akt signaling pathway, and on the Gene Ontology pathway, it is the Heme binding. The top 3 targets docked to quercetin have a certain affinity when it is docked to their degree value. Among the chemical components of Sanqi, quercetin has the most targets, suggesting that it may play a major role in the treatment of EMS. CONCLUSION: The results of molecular docking provide further evidence of the potential role of Sanqi for EMS. Overall, our study provides a new direction for the treatment of EMS and provides the basis for Sanqi as a drug for the treatment of EMS. |
format | Online Article Text |
id | pubmed-9478308 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-94783082022-09-19 Research into the mechanism of intervention of SanQi in endometriosis based on network pharmacology and molecular docking technology Lin, Zhiheng Fan, Weisen Yu, Xiao Liu, Jinxing Liu, Pengfei Medicine (Baltimore) Research Article By using network pharmacology and molecular docking technology, we have explored the mechanism of action of Sanqi in the treatment of endometriosis (EMS), in order to provide reference for clinical studies of Chinese medicine treatment of Ems and Chinese medicine pharmacology. METHODS: There are 123 intersecting targets between the active ingredients of Sanqi and disease targets. In the Protein-Protein Interaction network, Jun proto-oncogene, AP-1 transcription factor subunit, tumor necrosis factor, interleukin 6, etc., are the core proteins. The top 20 genes ranked by degree have been analyzed according to the Kyoto Encyclopedia of Genes and Genomes pathway and Gene Ontology analysis, and 20 pathways have been identified. RESULTS: On the Kyoto Encyclopedia of Genes and Genomes pathway, the most important part is the phosphatidylinositol 3’-kinase-Akt signaling pathway, and on the Gene Ontology pathway, it is the Heme binding. The top 3 targets docked to quercetin have a certain affinity when it is docked to their degree value. Among the chemical components of Sanqi, quercetin has the most targets, suggesting that it may play a major role in the treatment of EMS. CONCLUSION: The results of molecular docking provide further evidence of the potential role of Sanqi for EMS. Overall, our study provides a new direction for the treatment of EMS and provides the basis for Sanqi as a drug for the treatment of EMS. Lippincott Williams & Wilkins 2022-09-16 /pmc/articles/PMC9478308/ /pubmed/36123943 http://dx.doi.org/10.1097/MD.0000000000030021 Text en Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Lin, Zhiheng Fan, Weisen Yu, Xiao Liu, Jinxing Liu, Pengfei Research into the mechanism of intervention of SanQi in endometriosis based on network pharmacology and molecular docking technology |
title | Research into the mechanism of intervention of SanQi in endometriosis based on network pharmacology and molecular docking technology |
title_full | Research into the mechanism of intervention of SanQi in endometriosis based on network pharmacology and molecular docking technology |
title_fullStr | Research into the mechanism of intervention of SanQi in endometriosis based on network pharmacology and molecular docking technology |
title_full_unstemmed | Research into the mechanism of intervention of SanQi in endometriosis based on network pharmacology and molecular docking technology |
title_short | Research into the mechanism of intervention of SanQi in endometriosis based on network pharmacology and molecular docking technology |
title_sort | research into the mechanism of intervention of sanqi in endometriosis based on network pharmacology and molecular docking technology |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9478308/ https://www.ncbi.nlm.nih.gov/pubmed/36123943 http://dx.doi.org/10.1097/MD.0000000000030021 |
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