转录组学数据的综合生物信息学分析揭示枢纽基因作为非肌肉与肌肉浸润性膀胱癌的诊断生物标志物

Michail Sarafidis, G. Lambrou, G. Matsopoulos, D. Koutsouris
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引用次数: 0

摘要

膀胱癌(BCa)是世界上最常见的癌症之一,具有很高的社会经济影响。BCa可以表现为复发的非侵袭性和通常非肌肉侵袭性(NMIBC)肿瘤,需要慢性侵袭性监测,或具有高死亡率的侵袭性和肌肉侵袭性(MIBC)肿瘤。这两种亚型表现出不同的预后,需要不同的治疗方法。在本研究中,我们进行了综合生物信息学分析,结合来自各种微阵列实验的转录组学数据,以揭示两种亚型之间差异表达基因(DEGs)的共同特征。随后,我们构建了DEGs的蛋白-蛋白相互作用(PPI)网络,并基于11种拓扑分析方法定义了枢纽基因。然后,利用LASSO逻辑回归算法鉴定出最显著的枢纽基因。最后将选择的基因作为特征在支持向量机和随机森林的监督分类算法中进行BCa亚型识别。模型评估显示,在分离NMIBC和MIBC肿瘤方面,曲线下面积(AUC)值高达96%。驱动肿瘤亚型之间分离的基因可能被证明是BCa发展和进展的重要生物标志物,并最终成为治疗靶向的候选物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Integrative Bioinformatics Analysis of Transcriptomic Data Reveals Hub Genes as Diagnostic Biomarkers for Non-Muscle vs. Muscle Invasive Bladder Cancer
Bladder cancer (BCa) is one of the most prevalent cancers worldwide and accounts for high socioeconomic impact. BCa can manifest in the form of nonaggressive and usually non-muscle invasive (NMIBC) tumors that recur and require chronic invasive surveillance, or aggressive and muscle invasive (MIBC) tumors with high associated mortality. These two subtypes exhibit distinct prognosis and require different therapeutic approaches. In the present study, we conducted an integrative bioinformatics analysis, combining transcriptomic data from various microarray experiments, in order to reveal a common signature of differentially expressed genes (DEGs) between the two subtypes. Subsequently, we constructed the protein-protein interaction (PPI) network of the DEGs and defined the hub genes based on 11 topological analysis methods. Then, the most significant hub genes were identified using LASSO logistic regression algorithm. The selected genes were finally used as features in supervised classification algorithms, namely support vector machines and random forests, for BCa subtype discrimination. The models' evaluation showed area under the curve (AUC) values up to 96% as regards separating NMIBC from MIBC tumors. Genes driving the separation between tumor subtypes may prove to be important biomarkers for BCa development and progression, and eventually candidates for therapeutic targeting.
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