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基于转录组学的生物信息学方法探索脂多糖诱导的脓毒症心肌病的潜在治疗药物。

Exploring potential therapeutic agents for lipopolysaccharide-induced septic cardiomyopathy based on transcriptomics using bioinformatics.

机构信息

Department of Emergency, The First Affiliated Hospital of Fujian Medical University, Fujian, Fuzhou, 350005, China.

Fujian Hypertension Research Institute, The First Affiliated Hospital of Fujian Medical University, Fujian, Fuzhou, 350005, China.

出版信息

Sci Rep. 2023 Nov 23;13(1):20589. doi: 10.1038/s41598-023-47699-0.

Abstract

Septic cardiomyopathy (SCM) is a common and severe complication of sepsis, characterized by left ventricular dilation and reduced ejection fraction leading to heart failure. The pathogenesis of SCM remains unclear. Understanding the SCM pathogenesis is essential in the search for effective therapeutic agents for SCM. This study was to investigate the pathophysiology of SCM and explore new therapeutic drugs by bioinformatics. An SCM rat model was established by injection of 10 mg/kg lipopolysaccharide (LPS) for 24 h, and the myocardial tissues were collected for RNA sequencing. The differentially expressed genes (DEGs) between LPS rats and control (Ctrl) with the thresholds of |log2|≥ 1 and P < 0.05. A protein-protein interaction (PPI) network was constructed based on the DEGs. The hub genes were identified using five algorithms of Cytoscape in the PPI networks and validated in the GSE185754 dataset and by RT-qPCR. The hub genes were analyzed by Gene ontology (GO) analysis and Kyoto Encyclopedia of Genes and Genomes (KEGG), as well as Gene set enrichment analyses (GSEA). In addition, the miRNAs of hub genes were predicted through miRWalk, and the candidate therapeutic drugs were identified using the Connectivity Map (CMAP) database. This study revealed the identified hub genes (Itgb1, Il1b, Rac2, Vegfa) and key miRNAs (rno-miR-541-5p, rno-miR-487b-3p, rno-miR-1224, rno-miR-378a-5p, rno-miR-6334, and rno-miR-466b-5p), which were potential biological targets and biomarkers of SCM. Anomalies in cytokine-cytokine receptor interactions, complement and coagulation cascades, chemokine signaling pathways, and MAPK signaling pathways also played vital roles in SCM pathogenesis. Two high-confidence candidate compounds (KU-0063794 and dasatinib) were identified from the CMAP database as new therapeutic drugs for SCM. In summary, these four identified hub genes and enrichment pathways may hold promise for diagnosing and treating SCM.

摘要

脓毒症性心肌病(SCM)是脓毒症的一种常见且严重的并发症,其特征为左心室扩张和射血分数降低导致心力衰竭。SCM 的发病机制尚不清楚。了解 SCM 的发病机制对于寻找 SCM 的有效治疗药物至关重要。本研究通过生物信息学方法探讨 SCM 的病理生理学,并探索新的治疗药物。通过注射 10mg/kg 脂多糖(LPS)24 小时建立 SCM 大鼠模型,并收集心肌组织进行 RNA 测序。采用|log2|≥1 和 P<0.05 的阈值筛选 LPS 大鼠与对照(Ctrl)之间的差异表达基因(DEGs)。基于 DEGs 构建蛋白质-蛋白质相互作用(PPI)网络。使用 Cytoscape 中的五种算法在 PPI 网络中识别枢纽基因,并在 GSE185754 数据集和 RT-qPCR 中进行验证。通过基因本体(GO)分析和京都基因与基因组百科全书(KEGG)以及基因集富集分析(GSEA)对枢纽基因进行分析。此外,通过 miRWalk 预测枢纽基因的 microRNA(miRNA),并使用连接图谱(CMAP)数据库鉴定候选治疗药物。本研究揭示了鉴定出的枢纽基因(Itgb1、Il1b、Rac2、Vegfa)和关键 miRNA(rno-miR-541-5p、rno-miR-487b-3p、rno-miR-1224、rno-miR-378a-5p、rno-miR-6334 和 rno-miR-466b-5p),它们可能是 SCM 的潜在生物学靶点和生物标志物。细胞因子-细胞因子受体相互作用、补体和凝血级联、趋化因子信号通路和 MAPK 信号通路的异常也在 SCM 发病机制中发挥重要作用。从 CMAP 数据库中鉴定出两种高置信度候选化合物(KU-0063794 和 dasatinib)作为 SCM 的新治疗药物。总之,这四个鉴定出的枢纽基因和富集通路可能为 SCM 的诊断和治疗提供新的思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e179/10667505/c2b1078231b7/41598_2023_47699_Fig1_HTML.jpg

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