Center for Medical Laboratory Science, Affiliated Hospital of Youjiang Medical University for Nationalities, Guangxi, China.
Baise Key Laboratory for Research and Development on Clinical Molecular Diagnosis for High-Incidence Diseases, Guangxi, China.
Medicine (Baltimore). 2024 Nov 29;103(48):e40677. doi: 10.1097/MD.0000000000040677.
The high incidence, disability, mortality, and recurrence rates of cerebral infarction impose a heavy burden on both the Chinese and global populations. It is essential for the early diagnosis, prevention, and protection against brain cell injury. To identify differentially expressed microRNAs (miRNAs) in plasma exosomes of patients with cerebral ischemic stroke, determine relevant biomarkers, and explore their potential signaling pathways. High-throughput sequencing was used to detect the expression of plasma exosomal miRNAs in patients with cerebral ischemic stroke and in a control group. Gene Ontology, Kyoto Encyclopedia of Genes and Genomes enrichment, and target gene network analyses were performed to investigate the target genes and signaling pathways of the differentially expressed miRNAs. The sequencing results identified 95 differentially expressed miRNAs, with 40 upregulated and 55 downregulated miRNAs. Among these, hsa-miR-1303, hsa-miR-125b-1-3p, and hsa-miR-548ab were significantly upregulated in the stroke group and downregulated in the normal control group, whereas hsa-miR-1289 was downregulated in the stroke group and upregulated in the normal group. Gene Ontology, Kyoto Encyclopedia of Genes, and genomes enrichment analyses indicated that the differentially expressed miRNAs and their target genes were mainly concentrated in the PI3K-AKt, mitogen-activated protein kinase, calcium, Ras, Rap1, and cAMP signaling pathways. The expression of plasma exosomal hsa-miR-1303, hsa-miR-125b-1-3p, and hsa-miR-1289 was significantly different in stroke patients than in the control group. These miRNAs may be involved in various signaling pathways related to cerebral infarction, providing a reference for further experimental research.
脑梗死的高发病率、致残率、死亡率和复发率给中国乃至全球人群带来了沉重的负担。早期诊断、预防和保护脑细胞损伤至关重要。为了鉴定脑梗死患者血浆外泌体中差异表达的 microRNAs(miRNAs),确定相关的生物标志物,并探索其潜在的信号通路。采用高通量测序技术检测脑梗死患者和对照组血浆外泌体中 miRNA 的表达。进行基因本体论、京都基因与基因组百科全书富集分析和靶基因网络分析,以研究差异表达 miRNA 的靶基因和信号通路。测序结果共鉴定出 95 个差异表达的 miRNAs,其中 40 个上调,55 个下调。其中,hsa-miR-1303、hsa-miR-125b-1-3p 和 hsa-miR-548ab 在中风组中显著上调,而在正常对照组中下调;hsa-miR-1289 在中风组中下调,而在正常组中上调。基因本体论、京都基因与基因组百科全书富集分析表明,差异表达的 miRNAs 及其靶基因主要集中在 PI3K-Akt、丝裂原活化蛋白激酶、钙、Ras、Rap1 和 cAMP 信号通路。血浆外泌体 hsa-miR-1303、hsa-miR-125b-1-3p 和 hsa-miR-1289 在脑梗死患者中的表达与对照组相比差异显著。这些 miRNA 可能参与了与脑梗死相关的多种信号通路,为进一步的实验研究提供了参考。