Integrated multi-omics analysis and machine learning refine molecular subtypes and prognosis in hepatocellular carcinoma through O-linked glycosylation genes

IF 3.1 4区 生物学 Q1 GENETICS & HEREDITY
Minghao Li, Hongxu Li, Lei Liu, Qianyi Wei, Jie Gao, Bowen Hu, Zhihui Wang, Wenzhi Guo, Yi Zhang, Shuijun Zhang
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引用次数: 0

Abstract

O-glycosylation significantly influences cellular physiological processes and disease regulation by modulating the structure, function, and stability of proteins. However, there is a notable gap in research focusing on O-glycosylation in relation to the prognosis of HCC patients. The study aimed to explore the expression and function of O-glycosylation genes in HCC from both bulk- and single-cell perspectives. Multi-omics data related to O-glycosylation identified by weighted gene co-expression network analysis (WGCNA). This was then combined with ten different clustering algorithms to construct molecular subtypes of high-resolution HCC. Cancer subtype 1 (CS1) is characterized by significant genomic variation, moderate immune cell infiltration, and immune function enrichment. Patients with CS2 have a better prognosis and are characterized by a stable genomic structure, an immune-hot phenotype with rich immune cell infiltration, and sensitivity to immunotherapy. CS3 is characterized by poor prognosis, outstanding genomic instability, and an immune-cold phenotype, but can benefit more from treatment with drugs such as sorafenib, cisplatin, paclitaxel, and gemcitabine. To further emphasize the role of O-glycosylation genes in individual HCC patients, we employed 59 machine-learning methods to construct and assess prognostic traits with improved generalizability. Microarray results indicated a pronounced upregulation of glycosylation hub genes involved in HCC stratification and modeling within HCC tumorous tissues. Altogether, our study highlights the importance of O-glycosylation for the assessment of HCC prognosis and treatment options by redefining HCC subtypes and constructing a consensus machine learning-driven prognostic signature (CMLS). This research establishes an optimized decision-making platform that enables the precise stratification of HCC patients, refines tumor treatment plans, and predicts patient survivability, with broad clinical implications.

综合多组学分析和机器学习通过o -连锁糖基化基因改善肝细胞癌的分子亚型和预后。
o -糖基化通过调节蛋白质的结构、功能和稳定性,显著影响细胞生理过程和疾病调控。然而,关于o -糖基化与HCC患者预后关系的研究还存在明显的空白。本研究旨在从整体和单细胞角度探讨o -糖基化基因在HCC中的表达和功能。通过加权基因共表达网络分析(WGCNA)鉴定与o糖基化相关的多组学数据。然后将其与十种不同的聚类算法相结合,构建高分辨率HCC的分子亚型。癌症亚型1 (CS1)具有显著的基因组变异、适度的免疫细胞浸润和免疫功能富集的特征。CS2患者预后较好,具有基因组结构稳定、免疫热表型丰富、免疫细胞浸润、对免疫治疗敏感等特点。CS3的特点是预后差,突出的基因组不稳定性和免疫冷表型,但可以从索拉非尼、顺铂、紫杉醇和吉西他滨等药物治疗中获益更多。为了进一步强调o -糖基化基因在个体HCC患者中的作用,我们采用了59种机器学习方法来构建和评估预后特征,并提高了通用性。微阵列结果显示,在HCC肿瘤组织中参与HCC分层和建模的糖基化中心基因明显上调。总之,我们的研究通过重新定义HCC亚型和构建共识的机器学习驱动的预后特征(CMLS),强调了o -糖基化对HCC预后和治疗方案评估的重要性。本研究建立了一个优化的决策平台,可以实现HCC患者的精确分层,完善肿瘤治疗方案,预测患者的生存能力,具有广泛的临床意义。
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来源期刊
CiteScore
3.50
自引率
3.40%
发文量
92
审稿时长
2 months
期刊介绍: Functional & Integrative Genomics is devoted to large-scale studies of genomes and their functions, including systems analyses of biological processes. The journal will provide the research community an integrated platform where researchers can share, review and discuss their findings on important biological questions that will ultimately enable us to answer the fundamental question: How do genomes work?
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