Recurrently deregulated lncRNAs in hepatocellular carcinoma

Yang Yang(Center for Life Sciences), Lei Chen(Second Military Medical University), Jin Gu(Tsinghua University), Hanshuo Zhang(Peking University), Jiapei Yuan(Center for Life Sciences), Qiuyu Lian(Tsinghua University), Guishuai Lv(Second Military Medical University), Siqi Wang(Center for Life Sciences), Yang Wu(Center for Life Sciences), Yucheng Yang(Center for Life Sciences), Dongfang Wang(Center for Life Sciences), Yang Liu(Center for Life Sciences), Jing Tang(Wuhan General Hospital of Guangzhou), Guijuan Luo(Second Military Medical University), Yang Li(Center for Life Sciences), Long Hu(Center for Life Sciences), Xinbao Sun(Center for Life Sciences), Dong Wang(Center for Life Sciences), Mingzhou Guo(Chinese PLA General Hospital), Qiaoran Xi(Center for Life Sciences), Jianzhong Xi(Peking University), Hongyang Wang(Second Military Medical University), Michael Q. Zhang(The University of Texas at Dallas), Zhi John Lu(Center for Life Sciences)
Nature Communications
February 13, 2017
Cited by 383Open Access
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Abstract

Hepatocellular carcinoma (HCC) cells often invade the portal venous system and subsequently develop into portal vein tumour thrombosis (PVTT). Long noncoding RNAs (lncRNAs) have been associated with HCC, but a comprehensive analysis of their specific association with HCC metastasis has not been conducted. Here, by analysing 60 clinical samples' RNA-seq data from 20 HCC patients, we have identified and characterized 8,603 candidate lncRNAs. The expression patterns of 917 recurrently deregulated lncRNAs are correlated with clinical data in a TCGA cohort and published liver cancer data. Matched array data from the 60 samples show that copy number variations (CNVs) and alterations in DNA methylation contribute to the observed recurrent deregulation of 235 lncRNAs. Many recurrently deregulated lncRNAs are enriched in co-expressed clusters of genes related to cell adhesion, immune response and metabolic processes. Candidate lncRNAs related to metastasis, such as HAND2-AS1, were further validated using RNAi-based loss-of-function assays. Thus, we provide a valuable resource of functional lncRNAs and biomarkers associated with HCC tumorigenesis and metastasis.


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