利用免疫系统基因谱鉴定胶质瘤的预后和诊断生物标志物。

Q2 Medicine
Medical Journal of the Islamic Republic of Iran Pub Date : 2025-04-01 eCollection Date: 2025-01-01 DOI:10.47176/mjiri.39.49
Zahra Haghshenas, Elham Nazari, Ghazaleh Khalili-Tanha, Zahra Razzaghi
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引用次数: 0

摘要

背景:大约80%的恶性脑肿瘤和由原发性脑肿瘤引起的最常见的死亡原因属于胶质瘤。因此,识别早期诊断和预后的有效生物标志物对患者治疗具有重要影响。近年来,人们越来越多地使用机器学习(ML)来分析RNAseq数据,以识别新的癌症生物标志物。在这项研究中,通过从TCGA数据库收集患者数据并使用ML算法和生物信息学分析,确定了胶质瘤的诊断和预后生物标志物。方法:采用ML分析胶质瘤患者(GBMLGG)的核糖核酸(RNA)表达谱,鉴定差异表达基因(DEGs)。总的来说,本研究使用了1012名患者和35名对照,其中包括613名男性和434名女性。预后的生物标志物已通过生存曲线的Kaplan-Meier分析确定。我们还研究了deg的共表达、蛋白-蛋白相互作用(PPIs)以及deg与临床数据之间的相关性。采用受试者工作特征(ROC)曲线分析确定诊断指标。结果:经过归一化和滤波,我们鉴定出3172个deg, |FC|≥1,P < 0.0.05。生存分析显示,15个上调基因(GRAPL、LOC339240、LOC723809、NODAL、SILV、SPINK8、TAC4、ANG、CD209、F2RL2、LYZ、SLAMF7、psiTPTE22、SFRP4和DKFZP)和9个下调基因(PCDHGC5、CES8、CHD5、DNAJC6、DNM1、KIRREL3、NCOA7、RASAL1、SNCA)与总生存(OS)相关。此外,ML算法还鉴定出20个基因,其中PSD、TUBA4A和PCDHGC5被鉴定为具有高相关系数的候选基因。结论:总的来说,我们的研究结果表明免疫相关基因在胶质瘤的发生、发展和发病过程中起着至关重要的作用。五个免疫相关基因,包括SLAMF7、CD209、TAC4、HLA-DRB68和lyz,被发现是该疾病的诊断和预后生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification of Prognostic and Diagnostic Biomarkers for Glioma Utilizing Immune System Gene Profiling.

Background: Approximately 80% of all malignant brain tumors and the most common cause of death that occur as a result of primary brain tumors belong to glioma. Hence, identifying effective biomarkers for early diagnosis and prognosis can have a significant impact on patient treatment. Recent years have witnessed a significant increase in the use of machine learning (ML) to analyze RNAseq data to identify new cancer biomarkers. In this study, diagnostic and prognostic biomarkers for Glioma were identified through the collection of patient data from the TCGA database and analysis using ML algorithms and bioinformatics.

Methods: The study used ML to analyze ribonucleic acid (RNA) expression profiles from Glioma patients (GBMLGG) to identify differentially expressed genes (DEGs). In general, the sample of 1012 patients and 35 controls, which included 613 men and 434 women, was used in this study. Biomarkers of prognosis have been identified using the Kaplan-Meier analysis of survival curves. The coexpression of DEGs, protein-protein interactions (PPIs), and the correlation between DEGs and clinical data were also examined. The receiver operating characteristic (ROC) curve analysis was used to determine diagnostic markers.

Results: After normalization and filtering, we identified 3172 DEGs with a log fold change |FC| ≥ 1 and P < 0.0.05. According to a survival analysis, 15 upregulated genes (GRAPL, LOC339240, LOC723809, NODAL, SILV, SPINK8, TAC4, ANG, CD209, F2RL2, LYZ, SLAMF7, psiTPTE22, SFRP4 and DKFZP) and 9 downregulated genes (PCDHGC5, CES8, CHD5, DNAJC6, DNM1, KIRREL3, NCOA7, RASAL1, SNCA) were associated with overall survival (OS). In addition, the ML algorithm identified 20 genes, among which PSD, TUBA4A, and PCDHGC5 were identified as candidates with high correlation coefficients.

Conclusion: Generally, our results showed that immune-related genes play a crucial role in the development, progression, and pathogenesis of gliomas. Five immune-related genes-including SLAMF7, CD209, TAC4, HLA-DRB68, and LYZ-were found to be diagnostic and prognostic biomarkers of the disease.

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CiteScore
2.40
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