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探索多形性胶质母细胞瘤中转录组学和放射组学模式的预后价值及生物学途径。

Exploring the prognostic value and biological pathways of transcriptomics and radiomics patterns in glioblastoma multiforme.

作者信息

Luan Jixin, Zhang Di, Liu Bing, Yang Aocai, Lv Kuan, Hu Pianpian, Yu Hongwei, Shmuel Amir, Zhang Chuanchen, Ma Guolin

机构信息

Department of Radiology, China-Japan Friendship Hospital, Beijing, China.

China-Japan Friendship Hospital (Institute of Clinical Medical Sciences), Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.

出版信息

Heliyon. 2024 Jun 27;10(13):e33760. doi: 10.1016/j.heliyon.2024.e33760. eCollection 2024 Jul 15.

Abstract

OBJECTIVES

To develop a multi-omics prognostic model integrating transcriptomics and radiomics for predicting overall survival in patients with glioblastoma multiforme (GBM), and investigate the biological pathways of radiomics patterns.

MATERIALS AND METHODS

Transcription profiles of GBM patients and normal controls were used to obtain differentially expressed mRNAs and long non-coding RNAs (lncRNAs). Radiomics features were extracted from magnetic resonance imaging (MRI). Least absolute shrinkage and selection operator (LASSO) Cox regression was employed to select survival-associated features for the construction of transcriptomics and radiomics signatures. Genes associated with GBM prognosis were identified through the analysis of lncRNA-mRNA co-expression networks and Weighted Gene Co-expression Network Analysis (WGCNA), and their biological pathways were investigated using Genomes enrichment analysis. Transcriptomics, radiomics, and clinical data were integrated to evaluate the multi-omics prognostic model's performance.

RESULTS

LASSO Cox regression yielded 21 survival-related features, including 19 transcriptomics features and 2 radiomics features. Based on transcriptomics and radiomics signature, GBM patients were classified as high-risk or low-risk. The genes obtained from the co-expression network screen were associated with microtubule binding, while those from the WGCNA screen were associated with growth factor receptor binding. In the training set, the AUC values for the multi-omics model and clinical model were 0.964 and 0.830, respectively, while in the validation set, they were 0.907 and 0.787. The multi-omics prognostic model outperformed the clinical prognostic model.

CONCLUSIONS

The co-expression network and WGCNA methods revealed genes associated with multiple biological pathways in GBM. The multi-omics prognostic model demonstrated excellent performance and indicated significant potential for clinical application.

摘要

目的

开发一种整合转录组学和放射组学的多组学预后模型,用于预测多形性胶质母细胞瘤(GBM)患者的总生存期,并研究放射组学模式的生物学途径。

材料与方法

使用GBM患者和正常对照的转录谱来获取差异表达的mRNA和长链非编码RNA(lncRNA)。从磁共振成像(MRI)中提取放射组学特征。采用最小绝对收缩和选择算子(LASSO)Cox回归来选择与生存相关的特征,以构建转录组学和放射组学特征。通过lncRNA-mRNA共表达网络分析和加权基因共表达网络分析(WGCNA)鉴定与GBM预后相关的基因,并使用基因组富集分析研究其生物学途径。整合转录组学、放射组学和临床数据,以评估多组学预后模型的性能。

结果

LASSO Cox回归产生了21个与生存相关的特征,包括19个转录组学特征和2个放射组学特征。基于转录组学和放射组学特征,将GBM患者分为高风险或低风险。从共表达网络筛选中获得的基因与微管结合相关,而从WGCNA筛选中获得的基因与生长因子受体结合相关。在训练集中,多组学模型和临床模型的AUC值分别为0.964和0.830,而在验证集中,它们分别为0.907和0.787。多组学预后模型优于临床预后模型。

结论

共表达网络和WGCNA方法揭示了与GBM中多种生物学途径相关的基因。多组学预后模型表现出优异的性能,并显示出显著的临床应用潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15d8/11283067/7368ed97c884/gr1.jpg

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