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HDNA methylation data-based molecular subtype classification related to the prognosis of patients with hepatocellular carcinoma

机译:基于HDNA甲基化数据的分子亚型分类与肝细胞癌患者的预后相关

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摘要

DNA methylation is a common chemical modification of DNA in the carcinogenesis of hepatocellular carcinoma (HCC). In this bioinformatics analysis, 348 liver cancer samples were collected from the Cancer Genome Atlas (TCGA) database to analyse specific DNA methylation sites that affect the prognosis of HCC patients. 10,699 CpG sites (CpGs) that were significantly related to the prognosis of patients were clustered into 7 subgroups, and the samples of each subgroup were significantly different in various clinical pathological data. In addition, by calculating the level of methylation sites in each subgroup, 119 methylation sites (corresponding to 105 genes) were selected as specific methylation sites within the subgroups. Moreover, genes in the corresponding promoter regions in which the above specific methylation sites were located were subjected to signalling pathway enrichment analysis, and it was discovered that these genes were enriched in the biological pathways that were reported to be closely correlated with HCC. Additionally, the transcription factor enrichment analysis revealed that these genes were mainly enriched in the transcription factor KROX. A naive Bayesian classification model was used to construct a prognostic model for HCC, and the training and test data sets were used for independent verification and testing. This classification method can well reflect the heterogeneity of HCC samples and help to develop personalized treatment and accurately predict the prognosis of patients.
机译:DNA甲基化是肝细胞癌(HCC)致癌物中DNA的常用化学改性。在这种生物信息学分析中,从癌症基因组Atlas(TCGA)数据库中收集348个肝癌样品,分析影响HCC患者预后的特定DNA甲基化位点。与患者预后的10,699个CPG位点(CPG)聚集成7个亚组,各亚组的样品在各种临床病理数据中显着差异。另外,通过计算每个亚组中的甲基化位点的水平,选择119位甲基化位点(对应于105个基因)作为亚组内的特定甲基化位点。此外,对应于上述特定甲基化位点的相应启动子区域的基因进行信号传导途径富集分析,发现这些基因富集在据报道的生物途径中与HCC密切相关。另外,转录因子富集分析表明,这些基因主要富集在转录因子Krox中。用于构建HCC的预后模型的天真贝叶斯分类模型,训练和测试数据集用于独立验证和测试。这种分类方法可以很好地反映HCC样品的异质性,并有助于开发个性化治疗,并准确地预测患者的预后。

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