Construction of a ceRNA Network and a Prognostic lncRNA Signature associated with Vascular Invasion in Hepatocellular Carcinoma based on Weighted Gene Co-Expression Network Analysis

被引:12
|
作者
Tao, Haisu [1 ,2 ]
Li, Jiang [1 ,2 ]
Liu, Junjie [1 ,2 ]
Yuan, Tong [1 ,2 ]
Zhang, Erlei [1 ,2 ]
Liang, Huifang [1 ,2 ]
Huang, Zhiyong [1 ,2 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Hosp, Tongji Med Coll, Hepat Surg Ctr, Wuhan, Peoples R China
[2] Hubei Key Lab Hepatopancreato Biliary Dis, Wuhan, Peoples R China
来源
JOURNAL OF CANCER | 2021年 / 12卷 / 13期
基金
中国国家自然科学基金;
关键词
HCC; vascular invasion; ceRNA; prognostic signature; BBOX1-AS1; PROMOTES; METASTASIS; EMT; MICRORNAS; MIGRATION; SURVIVAL; GROWTH; CELLS;
D O I
10.7150/jca.57260
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Understanding risk factors for vascular invasion (VI) is crucial for assessing the risk of recurrence and overall prognosis of hepatocellular carcinoma (HCC). This study aimed to construct a prognostic long non-coding RNA (lncRNA) signature and a ceRNA Network associated with vascular invasion in HCC. Methods: Differentially expressed genes (DEGs) of HCC patients associated with VI were identified by analyzing data from TCGA. Weighted gene co-expression network analysis (WGCNA) was used to identify associations between gene expression modules and clinical features. A VI-related prognostic lncRNA signature was then established using univariate, LASSO and multivariate Cox proportional hazards regression analyses. Based on the hub modules identified by the WGCNA, we constructed a VI-related lncRNA-miRNA-mRNA ceRNA network and screened hub lncRNAs for further research. Finally, we conducted in vitro and in vivo experiments to determine the biological roles of the identified hub gene BBOX1-AS1. Results: The key module related to VI and OS was identified using WGCNA, after which a prognostic model consisting of eight lncRNAs was established, and verified using time-dependent receiver operating characteristic (ROC) curve analysis. BBOX1-AS1 was confirmed to be highly expressed in HCC tissues, and its expression was significantly correlated with a poor prognosis. Silencing BBOX1-AS1 in vitro significantly suppressed the proliferation, migration and invasion of HCC cells. In vivo experiments demonstrated that knocking down of BBOX1-AS1 could result in significant decrease of tumor volume and tumor weight. Conclusions: The VI-related lncRNA signature established in this study can be used to predict the clinical outcomes of HCC patients. In addition, we constructed a VI-related lncRNA-miRNA-mRNA ceRNA network and demonstrated that BBOX1-AS1 might be a novel biomarker associated with VI in HCC.
引用
收藏
页码:3754 / 3768
页数:15
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