Inferring Diagnostic and Prognostic Gene Expression Signatures Across WHO Glioma Classifications: A Network-Based Approach.

IF 2.3 Q3 BIOCHEMICAL RESEARCH METHODS
Bioinformatics and Biology Insights Pub Date : 2024-09-15 eCollection Date: 2024-01-01 DOI:10.1177/11779322241271535
Roberta Coletti, Mónica Leiria de Mendonça, Susana Vinga, Marta B Lopes
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引用次数: 0

Abstract

Tumor heterogeneity is a challenge to designing effective and targeted therapies. Glioma-type identification depends on specific molecular and histological features, which are defined by the official World Health Organization (WHO) classification of the central nervous system (CNS). These guidelines are constantly updated to support the diagnosis process, which affects all the successive clinical decisions. In this context, the search for new potential diagnostic and prognostic targets, characteristic of each glioma type, is crucial to support the development of novel therapies. Based on The Cancer Genome Atlas (TCGA) glioma RNA-sequencing data set updated according to the 2016 and 2021 WHO guidelines, we proposed a 2-step variable selection approach for biomarker discovery. Our framework encompasses the graphical lasso algorithm to estimate sparse networks of genes carrying diagnostic information. These networks are then used as input for regularized Cox survival regression model, allowing the identification of a smaller subset of genes with prognostic value. In each step, the results derived from the 2016 and 2021 classes were discussed and compared. For both WHO glioma classifications, our analysis identifies potential biomarkers, characteristic of each glioma type. Yet, better results were obtained for the WHO CNS classification in 2021, thereby supporting recent efforts to include molecular data on glioma classification.

在世界卫生组织胶质瘤分类中推断诊断和预后基因表达特征:基于网络的方法
肿瘤的异质性是设计有效靶向疗法的一大挑战。胶质瘤类型的确定取决于特定的分子和组织学特征,这些特征由世界卫生组织(WHO)的官方中枢神经系统(CNS)分类所定义。这些指南不断更新,以支持诊断过程,这影响到所有后续的临床决策。在这种情况下,寻找每种胶质瘤类型所特有的新的潜在诊断和预后靶点,对于支持新型疗法的开发至关重要。基于根据2016年和2021年世界卫生组织指南更新的癌症基因组图谱(TCGA)胶质瘤RNA测序数据集,我们提出了一种用于发现生物标志物的两步变量选择方法。我们的框架采用图形套索算法来估算携带诊断信息的稀疏基因网络。然后将这些网络作为正则化 Cox 生存回归模型的输入,从而识别出具有预后价值的较小基因子集。在每个步骤中,都对 2016 年和 2021 年分类得出的结果进行了讨论和比较。对于世界卫生组织的两种胶质瘤分类,我们的分析都确定了具有每种胶质瘤类型特征的潜在生物标志物。然而,2021 年世卫组织中枢神经系统分类的结果更好,从而支持了最近将分子数据纳入胶质瘤分类的努力。
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
Bioinformatics and Biology Insights
Bioinformatics and Biology Insights BIOCHEMICAL RESEARCH METHODS-
CiteScore
6.80
自引率
1.70%
发文量
36
审稿时长
8 weeks
期刊介绍: Bioinformatics and Biology Insights is an open access, peer-reviewed journal that considers articles on bioinformatics methods and their applications which must pertain to biological insights. All papers should be easily amenable to biologists and as such help bridge the gap between theories and applications.
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