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基于四甲基化mRNA特征的风险评分系统可预测肝细胞癌患者的生存率。

A four-methylated mRNA signature-based risk score system predicts survival in patients with hepatocellular carcinoma.

作者信息

Wang Yu, Ruan Zhiping, Yu Sizhe, Tian Tao, Liang Xuan, Jing Li, Li Wenyuan, Wang Xiao, Xiang Lcl, Claret F X, Nan Kejun, Guo Hui

机构信息

Department of Medical Oncology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, PR China.

Department of Systems Biology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.

出版信息

Aging (Albany NY). 2019 Jan 10;11(1):160-173. doi: 10.18632/aging.101738.

Abstract

Evidence suggests that altered DNA methylation plays a causative role in the pathogenesis of various cancers, including hepatocellular carcinoma (HCC). Thus, methylated differently expressed genes (MDEGs) could potentially serve as biomarkers and therapeutic targets in HCC. In the present study, screening four genomics profiling datasets (GSE62232, GSE84402, GSE73003 and GSE57956) enabled us to identify a total of 148 MDEGs. A signature was then established based on the top four MDEGs (BRCA1, CAD, CDC20 and RBM8A). Taking clinical variables into consideration, we constructed a risk score system consisting of the four-MDEG signature and the patients' clinical features, which was predictive of prognosis in HCC. The prognostic value of the HCC risk score system was confirmed using TCGA HCC samples. The scores were then used to construct a nomogram, performance of which was evaluated using Harrel's concordance index (C-index) and a calibration curve. The signature-based nomogram for prediction of overall survival in HCC patients exhibited good performance and was superior to traditional staging systems (C-index: 0.676 vs 0.629, P< 0.05). We have thus established a novel risk score system that is predictive of prognosis and is a potentially useful guide for personalized treatment of HCC patients.

摘要

有证据表明,DNA甲基化改变在包括肝细胞癌(HCC)在内的各种癌症的发病机制中起因果作用。因此,甲基化差异表达基因(MDEG)有可能作为HCC的生物标志物和治疗靶点。在本研究中,通过筛选四个基因组分析数据集(GSE62232、GSE84402、GSE73003和GSE57956),我们共鉴定出148个MDEG。然后基于前四个MDEG(BRCA1、CAD、CDC20和RBM8A)建立了一个特征。考虑到临床变量,我们构建了一个由四个MDEG特征和患者临床特征组成的风险评分系统,该系统可预测HCC的预后。使用TCGA HCC样本证实了HCC风险评分系统的预后价值。然后使用这些分数构建列线图,并使用Harrel一致性指数(C指数)和校准曲线评估其性能。基于特征的HCC患者总生存预测列线图表现良好,优于传统分期系统(C指数:0.676对0.629,P<0.05)。因此,我们建立了一种新的风险评分系统,该系统可预测预后,是HCC患者个性化治疗的潜在有用指南。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9654/6339794/5ed449a8fd2f/aging-11-101738-g001.jpg

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