冠心病治疗中药物反应性表型改变相关驱动基因的发现

IF 1.8 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pharmacogenomics & Personalized Medicine Pub Date : 2023-01-01 DOI:10.2147/PGPM.S398522
Shuang Guan, Ya-Nan Yu, Bing Li, Hao Gu, Lin Chen, Nian Wang, Bo Wang, Xi Liu, Jun Liu, Zhong Wang
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引用次数: 0

摘要

背景:血凝征(XYZ)表型是冠心病的核心,但检测XYZ表型的遗传关联的努力令人失望。方法:丹红注射液治疗后第14天、第30天,采用|ρ| > 0.4、p < 0.05筛选XYZ表型组的表型改变相关基因(PARGs)。然后,使用个性化网络控制算法(PNC)检测使用STRING 11.0建立的PARGs蛋白-蛋白相互作用(PPI)网络的驱动基因。最后,利用基因本体(GO)生物学过程和京都基因与基因组百科全书(KEGG)途径从整体角度分析了驱动基因与XYZ现象组的分子相关性。结果:在第14天和第30天,XYZ表型中共鉴定出525个和309个PARGs。这些基因分别在48条和35条途径中富集。此外,还检测到5个驱动基因。这些基因主要与内质网应激介导的细胞凋亡和自噬调控相关,可抑制动脉粥样硬化的进展。结论:我们的研究在冠心病患者中检测到XYZ表型的药物反应性PARGs,并提供了一种典型的策略来研究这种常见表型与其组成症状之间的遗传关联。试验注册:ClinicalTrials.gov, NCT01681316;于2012年9月7日注册。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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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 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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来源期刊
Pharmacogenomics & Personalized Medicine
Pharmacogenomics & Personalized Medicine Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
3.30
自引率
5.30%
发文量
110
审稿时长
16 weeks
期刊介绍: Pharmacogenomics and Personalized Medicine is an international, peer-reviewed, open-access journal characterizing the influence of genotype on pharmacology leading to the development of personalized treatment programs and individualized drug selection for improved safety, efficacy and sustainability. In particular, emphasis will be given to: Genomic and proteomic profiling Genetics and drug metabolism Targeted drug identification and discovery Optimizing drug selection & dosage based on patient''s genetic profile Drug related morbidity & mortality intervention Advanced disease screening and targeted therapeutic intervention Genetic based vaccine development Patient satisfaction and preference Health economic evaluations Practical and organizational issues in the development and implementation of personalized medicine programs.
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