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Discovery of Drug-Responsive Phenomic Alteration-Related Driver Genes in the Treatment of Coronary Heart Disease

BACKGROUND: The Xueyu Zheng (XYZ) phenome is central to coronary heart disease (CHD), but efforts to detect genetic associations in the XYZ phenome have been disappointing. METHODS: The phenomic alteration-related genes (PARGs) for the XYZ phenome were screened using |ρ| > 0.4 and p < 0.05 aft...

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Autores principales: Guan, Shuang, Yu, Ya-Nan, Li, Bing, Gu, Hao, Chen, Lin, Wang, Nian, Wang, Bo, Liu, Xi, Liu, Jun, Wang, Zhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10024908/
https://www.ncbi.nlm.nih.gov/pubmed/36945217
http://dx.doi.org/10.2147/PGPM.S398522
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author Guan, Shuang
Yu, Ya-Nan
Li, Bing
Gu, Hao
Chen, Lin
Wang, Nian
Wang, Bo
Liu, Xi
Liu, Jun
Wang, Zhong
author_facet Guan, Shuang
Yu, Ya-Nan
Li, Bing
Gu, Hao
Chen, Lin
Wang, Nian
Wang, Bo
Liu, Xi
Liu, Jun
Wang, Zhong
author_sort Guan, Shuang
collection PubMed
description BACKGROUND: The Xueyu Zheng (XYZ) phenome is central to coronary heart disease (CHD), but efforts to detect genetic associations in the XYZ phenome have been disappointing. METHODS: The phenomic alteration-related genes (PARGs) for the XYZ phenome were screened using |ρ| > 0.4 and p < 0.05 after treatment with Danhong injection at day 14 and day 30. Then, the driver genes for the Protein-Protein Interaction (PPI) networks of the PARGs established using STRING 11.0 were detected using a personalized network control algorithm (PNC). Finally, the molecular correlations of the driver genes with the XYZ phenome were analyzed with the Gene Ontology (GO) biological processes and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways from a holistic viewpoint. RESULTS: A total of 525 and 309 PARGs in the XYZ phenome at day 14 and day 30 were identified. These genes were separately enriched in 48 and 35 pathways. Furthermore, five driver genes were detected. These genes were mainly correlated with endoplasmic reticulum stress-mediated apoptosis and autophagy regulation, which could suppress atherosclerosis progression. CONCLUSION: Our study detected the drug-responsive PARGs of the XYZ phenome in CHD and provides an exemplary strategy to investigate the genetic associations among this common phenome and its component symptoms in patients with CHD. TRIAL REGISTRATION: ClinicalTrials.gov, NCT01681316; registered on September 7, 2012.
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spelling pubmed-100249082023-03-20 Discovery of Drug-Responsive Phenomic Alteration-Related Driver Genes in the Treatment of Coronary Heart Disease Guan, Shuang Yu, Ya-Nan Li, Bing Gu, Hao Chen, Lin Wang, Nian Wang, Bo Liu, Xi Liu, Jun Wang, Zhong Pharmgenomics Pers Med Original Research BACKGROUND: The Xueyu Zheng (XYZ) phenome is central to coronary heart disease (CHD), but efforts to detect genetic associations in the XYZ phenome have been disappointing. METHODS: The phenomic alteration-related genes (PARGs) for the XYZ phenome were screened using |ρ| > 0.4 and p < 0.05 after treatment with Danhong injection at day 14 and day 30. Then, the driver genes for the Protein-Protein Interaction (PPI) networks of the PARGs established using STRING 11.0 were detected using a personalized network control algorithm (PNC). Finally, the molecular correlations of the driver genes with the XYZ phenome were analyzed with the Gene Ontology (GO) biological processes and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways from a holistic viewpoint. RESULTS: A total of 525 and 309 PARGs in the XYZ phenome at day 14 and day 30 were identified. These genes were separately enriched in 48 and 35 pathways. Furthermore, five driver genes were detected. These genes were mainly correlated with endoplasmic reticulum stress-mediated apoptosis and autophagy regulation, which could suppress atherosclerosis progression. CONCLUSION: Our study detected the drug-responsive PARGs of the XYZ phenome in CHD and provides an exemplary strategy to investigate the genetic associations among this common phenome and its component symptoms in patients with CHD. TRIAL REGISTRATION: ClinicalTrials.gov, NCT01681316; registered on September 7, 2012. Dove 2023-03-15 /pmc/articles/PMC10024908/ /pubmed/36945217 http://dx.doi.org/10.2147/PGPM.S398522 Text en © 2023 Guan et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Guan, Shuang
Yu, Ya-Nan
Li, Bing
Gu, Hao
Chen, Lin
Wang, Nian
Wang, Bo
Liu, Xi
Liu, Jun
Wang, Zhong
Discovery of Drug-Responsive Phenomic Alteration-Related Driver Genes in the Treatment of Coronary Heart Disease
title Discovery of Drug-Responsive Phenomic Alteration-Related Driver Genes in the Treatment of Coronary Heart Disease
title_full Discovery of Drug-Responsive Phenomic Alteration-Related Driver Genes in the Treatment of Coronary Heart Disease
title_fullStr Discovery of Drug-Responsive Phenomic Alteration-Related Driver Genes in the Treatment of Coronary Heart Disease
title_full_unstemmed Discovery of Drug-Responsive Phenomic Alteration-Related Driver Genes in the Treatment of Coronary Heart Disease
title_short Discovery of Drug-Responsive Phenomic Alteration-Related Driver Genes in the Treatment of Coronary Heart Disease
title_sort discovery of drug-responsive phenomic alteration-related driver genes in the treatment of coronary heart disease
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10024908/
https://www.ncbi.nlm.nih.gov/pubmed/36945217
http://dx.doi.org/10.2147/PGPM.S398522
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