Deepening the Understanding of Platelet-Derived RNA as Biomarker for Glioblastoma Through GSEA, TDEA, and Elastic Net Regularization Analysis

IF 2.5 Q4 ONCOLOGY
Cancer reports Pub Date : 2026-09-30 DOI:10.1002/cnr2.70656
Anna Giczewska, Krzysztof Pastuszak, Leon van Hout, Edward Post, Jip Ramaker, Ken Zwaan, Anna Supernat, Bart A. Westerman
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Abstract

Background

Glioblastoma (GBM) is the most aggressive form of primary brain cancer. Blood platelets have emerged as biomarkers where their RNA expression pattern indicates a tumor's presence. Our study aimed to characterize these patterns to identify biological processes associated with GBM and to evaluate their potential as a non-invasive biomarker.

Methods

We analyzed platelet RNA-seq expression profiles from 84 GBM patients and 319 healthy individuals using two complementary analytical approaches of Gene Set Enrichment Analysis and Threshold-based Differential Expression Analysis with Elastic Net regularization. Together, these approaches may offer complementary perspectives on biological pathways associated with GBM and the descriptive functional annotation of a predictive platelet RNA gene signature, providing insight into platelet-tumor interactions.

Results

Our GSEA broad analysis highlighted platelet-related biological processes, including coagulation, wound healing, immune regulation, and cytoskeletal organization. The Elastic Net framework additionally suggested pathways related to immune activation, cell signaling, and protein folding. Overall, these findings may suggest that platelet-derived RNA not only has potential as a non-invasive biomarker but may also provide insight into the systemic biological processes associated with the GBM tumor microenvironment.

Conclusions

Our data suggests that platelet-derived RNA may reflect biological processes associated with the GBM tumor microenvironment, where wound repair and immune-related processes may play important roles. Our findings provide a resource for further research into the mechanisms that may underlie the pathophysiology and progression of glioblastoma.

通过GSEA、TDEA和弹性网正则化分析加深对血小板来源RNA作为胶质母细胞瘤生物标志物的认识
胶质母细胞瘤(GBM)是最具侵袭性的原发性脑癌。血小板已经成为生物标志物,其RNA表达模式表明肿瘤的存在。我们的研究旨在表征这些模式,以确定与GBM相关的生物过程,并评估其作为非侵入性生物标志物的潜力。方法采用基因集富集分析和基于阈值的弹性网正则化差异表达分析两种互补分析方法,分析84例GBM患者和319例健康人的血小板RNA-seq表达谱。总之,这些方法可以为与GBM相关的生物学途径和预测性血小板RNA基因标记的描述性功能注释提供补充观点,为血小板-肿瘤相互作用提供见解。我们的GSEA广泛分析强调了血小板相关的生物学过程,包括凝血、伤口愈合、免疫调节和细胞骨架组织。弹性网框架还提出了与免疫激活、细胞信号传导和蛋白质折叠相关的途径。总的来说,这些发现可能表明,血小板来源的RNA不仅具有作为一种非侵入性生物标志物的潜力,而且还可能提供与GBM肿瘤微环境相关的系统生物学过程的见解。我们的数据表明,血小板来源的RNA可能反映了与GBM肿瘤微环境相关的生物学过程,其中伤口修复和免疫相关过程可能发挥重要作用。我们的发现为进一步研究胶质母细胞瘤的病理生理和进展机制提供了资源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cancer reports
Cancer reports Medicine-Oncology
CiteScore
2.70
自引率
5.90%
发文量
160
审稿时长
17 weeks
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