DNA甲基化
转录组
组学
肝细胞癌
甲基化
计算生物学
生物
癌症
恶性肿瘤
生物信息学
基因
基因表达
癌症研究
遗传学
作者
Qiong Wu,Xubin Zheng,Kwong‐Sak Leung,Man‐Hon Wong,Stephen Kwok-Wing Tsui,Lixin Cheng
出处
期刊:Bioinformatics
[Oxford University Press]
日期:2022-06-08
卷期号:38 (14): 3513-3522
被引量:14
标识
DOI:10.1093/bioinformatics/btac379
摘要
Abstract Motivation Hepatocellular carcinoma (HCC) is a primary malignancy with a poor prognosis. Recently, multi-omics molecular-level measurement enables HCC diagnosis and prognosis prediction, which is crucial for early intervention of personalized therapy to diminish mortality. Here, we introduce a novel strategy utilizing DNA methylation and RNA expression data to achieve a multi-omics gene pair signature (GPS) for HCC discrimination. Results The immune genes with negative correlations between expression and promoter methylation are enriched in the highly connected cancer-related pathway network, which are considered as the candidates for HCC detection. After that, we separately construct a methylation GPS (mGPS) and an expression GPS (eGPS), and then assemble them as a meGPS with five gene pairs, in which the significant methylation and expression changes occur between HCC tumor and non-tumor groups. Reliable performance has been validated by independent tissue (age, gender and etiology) and blood datasets. This study proposes a procedure for multi-omics GPS identification and develops a novel HCC signature using both methylome and transcriptome data, suggesting potential molecular targets for the detection and therapy of HCC. Availability and implementation Models are available at https://github.com/bioinformaticStudy/meGPS.git. Supplementary information Supplementary data are available at Bioinformatics online.
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