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Investigation into the in vivo mechanism of diosmetin in patients with breast cancer and COVID-19 using bioinformatics
Patients with breast cancer are prone to SARS-CoV-2 infection [the causative virus of coronavirus disease (COVID-19)] due to their lack of immunity. In the current study, we examined the mechanism of action of Diosmetin, a flavonoid with anti-inflammatory properties, in patients with BRCA infected w...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9433109/ https://www.ncbi.nlm.nih.gov/pubmed/36060002 http://dx.doi.org/10.3389/fphar.2022.983821 |
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author | Wang, Jin Ma, Shanbo Li, Long Chen, Yuhan Yang, Qian Wang, Feiyan Zheng, Meiling Miao, Shan Shi, Xiaopeng |
author_facet | Wang, Jin Ma, Shanbo Li, Long Chen, Yuhan Yang, Qian Wang, Feiyan Zheng, Meiling Miao, Shan Shi, Xiaopeng |
author_sort | Wang, Jin |
collection | PubMed |
description | Patients with breast cancer are prone to SARS-CoV-2 infection [the causative virus of coronavirus disease (COVID-19)] due to their lack of immunity. In the current study, we examined the mechanism of action of Diosmetin, a flavonoid with anti-inflammatory properties, in patients with BRCA infected with SARS-CoV-2.We used bioinformatics technology to analyze the binding ability, biological function, and other biological characteristics of Diosmetin in vivo and examine the core target and potential mechanism of action of Diosmetin in patients with patients with breast cancer infected with SARS-CoV-2. A prognostic model of SARS-COV-2–infected breast cancer patients was constructed, and the core genes were screened out, revealing the correlation between these core genes and clinicopathological characteristics, survival rate, and high-risk and low-risk populations. The docking results revealed that Diosmetin binds well to the core genes of patients with breast cancer with COVID-19. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses suggested that Diosmetin inhibited inflammation, enhanced immune function, and regulated the cellular microenvironment in patients with BRCA/COVID-19. For the first time, we reveal the molecular functions and potential targets of Diosmetin in patients with breast cancer infected with SARS-CoV-2, improving the reliability of the new drug and laying the foundation for further research and development. |
format | Online Article Text |
id | pubmed-9433109 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94331092022-09-01 Investigation into the in vivo mechanism of diosmetin in patients with breast cancer and COVID-19 using bioinformatics Wang, Jin Ma, Shanbo Li, Long Chen, Yuhan Yang, Qian Wang, Feiyan Zheng, Meiling Miao, Shan Shi, Xiaopeng Front Pharmacol Pharmacology Patients with breast cancer are prone to SARS-CoV-2 infection [the causative virus of coronavirus disease (COVID-19)] due to their lack of immunity. In the current study, we examined the mechanism of action of Diosmetin, a flavonoid with anti-inflammatory properties, in patients with BRCA infected with SARS-CoV-2.We used bioinformatics technology to analyze the binding ability, biological function, and other biological characteristics of Diosmetin in vivo and examine the core target and potential mechanism of action of Diosmetin in patients with patients with breast cancer infected with SARS-CoV-2. A prognostic model of SARS-COV-2–infected breast cancer patients was constructed, and the core genes were screened out, revealing the correlation between these core genes and clinicopathological characteristics, survival rate, and high-risk and low-risk populations. The docking results revealed that Diosmetin binds well to the core genes of patients with breast cancer with COVID-19. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses suggested that Diosmetin inhibited inflammation, enhanced immune function, and regulated the cellular microenvironment in patients with BRCA/COVID-19. For the first time, we reveal the molecular functions and potential targets of Diosmetin in patients with breast cancer infected with SARS-CoV-2, improving the reliability of the new drug and laying the foundation for further research and development. Frontiers Media S.A. 2022-08-17 /pmc/articles/PMC9433109/ /pubmed/36060002 http://dx.doi.org/10.3389/fphar.2022.983821 Text en Copyright © 2022 Wang, Ma, Li, Chen, Yang, Wang, Zheng, Miao and Shi. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Wang, Jin Ma, Shanbo Li, Long Chen, Yuhan Yang, Qian Wang, Feiyan Zheng, Meiling Miao, Shan Shi, Xiaopeng Investigation into the in vivo mechanism of diosmetin in patients with breast cancer and COVID-19 using bioinformatics |
title | Investigation into the in vivo mechanism of diosmetin in patients with breast cancer and COVID-19 using bioinformatics |
title_full | Investigation into the in vivo mechanism of diosmetin in patients with breast cancer and COVID-19 using bioinformatics |
title_fullStr | Investigation into the in vivo mechanism of diosmetin in patients with breast cancer and COVID-19 using bioinformatics |
title_full_unstemmed | Investigation into the in vivo mechanism of diosmetin in patients with breast cancer and COVID-19 using bioinformatics |
title_short | Investigation into the in vivo mechanism of diosmetin in patients with breast cancer and COVID-19 using bioinformatics |
title_sort | investigation into the in vivo mechanism of diosmetin in patients with breast cancer and covid-19 using bioinformatics |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9433109/ https://www.ncbi.nlm.nih.gov/pubmed/36060002 http://dx.doi.org/10.3389/fphar.2022.983821 |
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