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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...

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Autores principales: Wang, Jin, Ma, Shanbo, Li, Long, Chen, Yuhan, Yang, Qian, Wang, Feiyan, Zheng, Meiling, Miao, Shan, Shi, Xiaopeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
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.
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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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