Bioinformatics Identification and Validation of Angiogenesis-Related Genes in Myocardial Ischemic Reperfusion Injury.

IF 3.3 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Frontiers in bioscience (Landmark edition) Pub Date : 2024-09-29 DOI:10.31083/j.fbl2910347
Longfei Wu, Zhijiang Zhou, Yuheng Zeng, Shengli Yang, Qingying Zhang
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Abstract

Background: Angiogenesis plays a critical protective role in myocardial ischemia-reperfusion injury (MIRI); however, therapeutic targeting of associated genes remains constrained. To bridge this gap, we conducted bioinformatics analysis to identify pivotal angiogenesis-related genes in MIRI, potentially applicable for preventive and therapeutic interventions.

Methods: We collected two mouse heart I/R expression datasets (GSE61592 and GSE83472) from Gene Expression Omnibus, utilizing the Limma package to identify differentially expressed genes (DEGs). Angiogenesis-related genes (ARGs) were extracted from GeneCards, and their overlap with DEGs produced differentially expressed ARGs (ARDEGs). Further analyses included Gene Ontology, Kyoto Encyclopedia of Genes and Genomes, and disease ontology to explore biological functions. Weighted gene correlation network analysis (WGCNA) was used to investigate molecular modules linked to MIRI. Additionally, a protein-protein interaction (PPI) network was constructed to pinpoint hub genes relevant to MIRI. Receiver operating characteristic curves were used to assess the diagnostic efficacy of these hub genes for MIRI. An ischemia-reperfusion injury model was established using human cardiac microvascular endothelial cells (HCMECs), with the expression of hub genes validated within this experimental framework.

Results: We identified 47 ARDEGs, 41 upregulated and 6 downregulated. PPI network analysis revealed suppressor of cytokine signaling 3 (Socs3), C-X-C motif chemokine ligand 1 (Cxcl1), interleukin 1 beta (Il1b), and matrix metallopeptidase 9 (Mmp9) as hub genes. Receiver operating characteristic (ROC) curve analysis demonstrated strong diagnostic potential for Socs3, Cxcl1, Il1b, and Mmp9. In vitro validation corroborated the mRNA and protein expression predictions.

Conclusions: Our study highlights the pivotal role of Socs3, Cxcl1, Il1b, and Mmp9 in MIRI development, their significance in immune cell infiltration, and their diagnostic accuracy. These findings offer valuable insights for MIRI diagnosis and treatment, presenting potential molecular targets for future research.

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心肌缺血再灌注损伤中血管生成相关基因的生物信息学鉴定与验证
背景:血管生成在心肌缺血再灌注损伤(MIRI)中起着关键的保护作用;然而,相关基因的治疗靶点仍然受到限制。为了弥合这一差距,我们进行了生物信息学分析,以确定心肌缺血再灌注损伤中与血管生成相关的关键基因,这些基因可能适用于预防和治疗干预:我们从基因表达总库(Gene Expression Omnibus)中收集了两个小鼠心脏I/R表达数据集(GSE61592和GSE83472),利用Limma软件包识别差异表达基因(DEGs)。从基因卡片(GeneCards)中提取血管生成相关基因(ARGs),与 DEGs 重叠后产生差异表达的 ARGs(ARDEGs)。进一步的分析包括基因本体、京都基因和基因组百科全书以及疾病本体,以探索生物功能。加权基因相关网络分析(WGCNA)用于研究与 MIRI 相关的分子模块。此外,还构建了蛋白质-蛋白质相互作用(PPI)网络,以确定与 MIRI 相关的枢纽基因。受体操作特征曲线用于评估这些中心基因对 MIRI 的诊断效果。利用人体心脏微血管内皮细胞(HCMECs)建立了缺血再灌注损伤模型,并在此实验框架内验证了中心基因的表达:结果:我们发现了 47 个 ARDEGs,其中 41 个上调,6 个下调。PPI 网络分析显示细胞因子信号转导抑制因子 3(Socs3)、C-X-C 矩阵趋化因子配体 1(Cxcl1)、白细胞介素 1 beta(Il1b)和基质金属肽酶 9(Mmp9)是枢纽基因。接收操作特征(ROC)曲线分析表明,Socs3、Cxcl1、Il1b 和 Mmp9 具有很强的诊断潜力。体外验证证实了 mRNA 和蛋白质表达预测:我们的研究强调了 Socs3、Cxcl1、Il1b 和 Mmp9 在 MIRI 发病中的关键作用、它们在免疫细胞浸润中的重要性及其诊断准确性。这些发现为 MIRI 的诊断和治疗提供了有价值的见解,为今后的研究提供了潜在的分子靶点。
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