Changchun University of Chinese Medicine, No.1035 Boshuo Road, Jing Yue National High-Tech Industrial Development Zone, Changchun, 130117, China.
School of Aeronautical Fundamentals, Aviation University of Air Force, Changchun, 130041, China.
Sci Rep. 2023 Apr 20;13(1):6492. doi: 10.1038/s41598-023-33059-5.
We aimed to identify the immune and Toll-like receptor (TLR) signaling pathway related feature lncRNAs to construct the diagnostic nomograms for acute ischemic stroke (AIS). Two AIS-associated expression profiles GSE16561 and GSE22255 were downloaded from NCBI Gene Expression Omnibus, the former was the training set and the latter was the validation set. The differential expression genes (DEGs) and lncRNAs (DElncRNAs) related to TLR signaling pathway were identified between AIS and control groups. The single sample gene set enrichment analysis (ssGSEA) was applied to evaluate the immune infiltration. The immune and TLR signaling pathway related DElncRNAs were determined. Three optimization algorithms were utilized to select the immune and TLR signaling pathway related feature lncRNAs to construct the diagnostic nomograms of AIS. Based on the lncRNA signature, a ceRNA network was constructed. 37 DEGs and 28 DElncRNAs related to TLR signaling pathway were identified in GSE16561. 16 immune cell types exhibited significant differences in distribution between AIS and control groups. 28 immune and TLR signaling pathway related DElncRNAs were determined. 8 immune and TLR signaling pathway related feature lncRNAs were selected. The diagnostic nomograms of AIS performed well in both datasets. A ceRNA network was constructed consisting of 7 immune and TLR signaling pathway related feature lncRNAs as well as 19 AIS related miRNAs and 21 TLR signaling pathway related genes. LINC00173, LINC01089, LINC02210, MIR600HG, SNHG14, TP73-AS1, LINC00680 and CASC2 may be the potential biomarkers of AIS diagnosis, and TLR signaling pathway may be a promising immune related therapeutic target for AIS.
我们旨在鉴定与免疫和 Toll 样受体(TLR)信号通路相关的特征 lncRNAs,以构建急性缺血性脑卒中(AIS)的诊断列线图。从 NCBI Gene Expression Omnibus 下载了两个与 AIS 相关的表达谱 GSE16561 和 GSE22255,前者为训练集,后者为验证集。在 AIS 组和对照组之间鉴定与 TLR 信号通路相关的差异表达基因(DEGs)和 lncRNAs(DElncRNAs)。应用单样本基因集富集分析(ssGSEA)评估免疫浸润情况。确定与免疫和 TLR 信号通路相关的 DElncRNAs。利用三种优化算法选择与免疫和 TLR 信号通路相关的特征 lncRNAs,构建 AIS 的诊断列线图。基于 lncRNA 特征,构建 ceRNA 网络。在 GSE16561 中鉴定出与 TLR 信号通路相关的 37 个 DEG 和 28 个 DElncRNA。16 种免疫细胞类型在 AIS 组和对照组之间的分布存在显著差异。确定了 28 个与免疫和 TLR 信号通路相关的 DElncRNAs。选择了 8 个与免疫和 TLR 信号通路相关的特征 lncRNAs。AIS 的诊断列线图在两个数据集上均表现良好。构建了一个由 7 个与免疫和 TLR 信号通路相关的特征 lncRNA、19 个与 AIS 相关的 miRNA 和 21 个 TLR 信号通路相关基因组成的 ceRNA 网络。LINC00173、LINC01089、LINC02210、MIR600HG、SNHG14、TP73-AS1、LINC00680 和 CASC2 可能是 AIS 诊断的潜在生物标志物,TLR 信号通路可能是 AIS 免疫相关治疗的有前途的靶点。