International Journal of General Medicine (Jul 2023)

Uncovering Candidate mRNAs, Signaling Pathways and Immune Cells in Atherosclerotic Plaque and Ischemic Stroke

  • Zhang X,
  • Han T,
  • Xu T,
  • Wang H,
  • Ma H

Journal volume & issue
Vol. Volume 16
pp. 2999 – 3012

Abstract

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Xianjing Zhang,1,* Tingting Han,1,* Tengxiao Xu,1 Huimin Wang,1 Haijun Ma2 1Department of Emergency Medicine, The Second Affiliated Hospital of Shandong First Medical University, Taian, 271000, People’s Republic of China; 2Department of Radiology, Taian Maternity and Child Health Care Hospital, Taian, 271000, People’s Republic of China*These authors contributed equally to this workCorrespondence: Haijun Ma, Department of Radiology, Taian Maternity and Child Health Care Hospital, 386 Long Tan Nan Road, Taian, 271000, People’s Republic of China, Tel +86-13583801283, Email [email protected]: The specific molecular mechanistic link between atherosclerotic plaques and ischemic stroke (IS) is not clear. The aim of this study is to explore the potential molecular relationship between atherosclerotic plaques and IS.Methods: All data were downloaded from the Gene Expression Omnibus (GEO) database. Key hub differentially expressed mRNAs (DEmRNAs) related to atherosclerotic plaques and IS were identified by differential expression analysis and least absolute shrinkage and selection operator (LASSO) analysis. Subsequently, a diagnostic model was established based on the expression of key hub DEmRNAs and logistic regression. In order to understand the molecular mechanism of key hub DEmRNAs, the transcription factor (TF) regulatory network and mRNA-miRNA-lncRNA regulatory network were also constructed. In addition, functional enrichment analysis and single-sample Gene Set Enrichment Analysis (ssGSEA) analysis were also performed.Results: Four key hub DEmRNAs (ADCY3, CLDN7, PPM1B and RRAS2) were identified by differential expression analysis and LASSO analysis. Moreover, the diagnostic model based on four key hub DEmRNAs has excellent diagnostic accuracy. We also found that Type 1 T helper cell may be associated with IS caused by atherosclerosis based on ssGSEA analysis. In the mRNA-miRNA-lncRNA regulatory network, we found that multiple signaling axes such as RRAS2-hsa-miR-3150b-3p-ILF3-AS1, PPM1B-hsa-miR-541-5p-LINC00294, CLDN7-hsa-miR-184-LINC00467 and ADCY3-hsa-miR-488-3p-URB1-AS1 may play an important role in the progression of IS. In addition, some signaling pathways, including chemokine signaling pathway, MAPK signaling pathway and cAMP signaling pathway, may be involved in regulating IS.Conclusion: The identified key molecules, signaling pathways and immune cells may help to provide a theoretical basis for exploring the relationship between atherosclerotic plaque and the progression of IS.Keywords: ischemic stroke, atherosclerotic plaques, diagnostic accuracy, Type 1 T helper cell, functional enrichment, mRNA-miRNA-lncRNA regulatory network

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