期刊
EUROPEAN NEUROLOGY
卷 85, 期 2, 页码 148-161出版社
KARGER
DOI: 10.1159/000518893
关键词
Cerebral infarction; Differentially expressed microRNAs; mRNAs; Immunocyte infiltration; Diagnosis; Therapy
资金
- key project of Hebei Province medical science research [20191480]
The study identified 17 differentially expressed miRNAs and 3,267 differentially expressed mRNAs, with 310 significantly associated with immunocyte subtypes. Several miRNA-mRNA-immunocyte subtype networks were established, revealing potential diagnostic targets for cerebral infarction.
Introduction: Cerebral infarction (CI) is one of the leading causes of serious long-term disability and mortality. Objective: We aimed to identify potential miRNAs and target mRNAs and assess the involvement of immunocyte infiltration in the process of CI. Methods: First, miRNA and mRNA data were downloaded from the Gene Expression Omnibus database, followed by differential expression analysis. Second, correlation analysis between differentially expressed mRNAs and differential immunocyte subtypes was performed through the CIBERSORT algorithm. Third, the regulatory network between miRNAs and immunocyte subtype-related mRNAs was constructed followed by the functional analysis of these target mRNAs. Fourth, correlation validation between differentially expressed mRNAs and differential immunocyte subtypes was performed in the GSE37587 dataset. Finally, the diagnostic ability of immunocyte subtype-related mRNAs was tested. Results: Up to 17 differentially expressed miRNAs and 3,267 differentially expressed mRNAs were identified, among which 310 differentially expressed mRNAs were significantly associated with immunocyte subtypes. Several miRNA-target mRNA-immunocyte subtype networks including hsa-miR-671-3p-ZC3HC1-neutrophils, hsa-miR-625-CD5-monocytes, hsa-miR-122-ACOX1/DUSP1/NEDD9-neutrophils, hsa-miR-455-5p-SLC24A4-monocytes, and hsa-miR-455-5p-SORL1-neutrophils were identified. LAT, ACOX1, DUSP1, NEDD9, ZC3HC1, BIN1, AKT1, DNMT1, SLC24A4, and SORL1 had a potential diagnostic value for CI. Conclusions: The network including miRNA, target mRNA, and immunocyte subtype may be novel regulators and diagnostic and therapeutic targets in CI.
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