Poursheikhani Arash, Mosallaei Meysam, Heidari Mohammad Foad, Rajaeinejad Mohsen, Chamanara Mohsen, Yousefi Zoshk Mojtaba, Aslani Peyman, Hazrati Ebrahim, Mohammadimehr Mojgan, Behroozi Javad
Department of Genetics and Advanced Medical Technology, Faculty of Medicine, AJA University of Medical Sciences, Tehran, Iran.
Legal Medicine Research Center, Legal Medicine Organization, Tehran, Iran.
Iran J Public Health. 2024 Sep;53(9):2090-2102. doi: 10.18502/ijph.v53i9.16462.
Glioblastoma multiforme (GBM) is one of the most invasive types of brain cancer. LncRNAs can be considered a new prognostic and diagnostic biomarker in GBM. This study comprehensively explored the interaction of lncRNAs with mRNAs in the TCGA database and proposed a novel promising biomarker with favorable diagnostic and prognostic values.
The public data of RNA-seq and related clinical data were downloaded from the TCGA database. Differential expression analysis was conducted in R. GO and KEGG signaling pathways were used for enrichment. The STRING database was used for PPI analysis. CE-network was constructed by STAR database. Kaplan-Meier survival analysis and ROC curve analysis to indicate the biomarkers' diagnostic and prognostic values.
Differentially expressed data illustrated that 4428 mRNAs were differentially expressed in GBM. The GO and KEGG pathway analysis showed that the differentially expressed mRNAs were enriched in critical biological processes. The PPI showed that and were the important PPI hubs. The ceRNA network data demonstrated critical lncRNAs. The data revealed that the lncRNA , , , and are potential diagnostic prognostic biomarkers in the GBM patients.
Altogether, we demonstrated lncRNA, and mRNA interaction and mentioned regulatory networks, considered a therapeutic option in GBM. In addition, we proposed potential diagnostic and prognostic biomarkers for the patients.
多形性胶质母细胞瘤(GBM)是最具侵袭性的脑癌类型之一。长链非编码RNA(lncRNAs)可被视为GBM中一种新的预后和诊断生物标志物。本研究全面探索了TCGA数据库中lncRNAs与mRNAs的相互作用,并提出了一种具有良好诊断和预后价值的新型有前景的生物标志物。
从TCGA数据库下载RNA测序的公共数据及相关临床数据。在R中进行差异表达分析。使用GO和KEGG信号通路进行富集分析。利用STRING数据库进行蛋白质-蛋白质相互作用(PPI)分析。通过STAR数据库构建竞争性内源RNA(ceRNA)网络。进行Kaplan-Meier生存分析和ROC曲线分析以表明生物标志物的诊断和预后价值。
差异表达数据表明,4428个mRNA在GBM中差异表达。GO和KEGG通路分析显示,差异表达的mRNA在关键生物学过程中富集。PPI分析表明[具体蛋白名称1]和[具体蛋白名称2]是重要的PPI枢纽。ceRNA网络数据显示了关键的lncRNAs。数据表明lncRNA[具体lncRNA名称1]、[具体lncRNA名称2]、[具体lncRNA名称3]、[具体lncRNA名称4]和[具体lncRNA名称5]是GBM患者潜在的诊断和预后生物标志物。
总之,我们展示了lncRNA与mRNA的相互作用并提及了调控网络,这被认为是GBM的一种治疗选择。此外,我们为患者提出了潜在的诊断和预后生物标志物。