Novel risk model based on angiogenesis-related lncRNAs for prognosis prediction of hepatocellular carcinoma

被引:0
作者
Shicheng Xie
Jinwei Zhong
Zhongjing Zhang
Weiguo Huang
Xiaoben Lin
Yating Pan
Xiuyan Kong
Hongping Xia
Zhijie Yu
Haizhen Ni
Jinglin Xia
机构
[1] The First Affiliated Hospital of Wenzhou Medical University,Key Laboratory of Diagnosis and Treatment of Severe Hepato
[2] The First Affiliated Hospital of Wenzhou Medical University,Pancreatic Diseases of Zhejiang Province
[3] The First Affiliated Hospital of Wenzhou Medical University,Department of Vascular Surgery
[4] The First Affiliated Hospital of Wenzhou Medical University,Wenzhou Key Laboratory of Hematology
[5] Fudan University,Department of Interventional Radiology
[6] Zhongda Hospital,Liver Cancer Institute, Zhongshan Hospital
[7] Southeast University,School of Medicine & Advanced Institute for Life and Health
来源
Cancer Cell International | / 23卷
关键词
Hepatocellular carcinoma; lncRNA; Machine learning; Angiogenesis; MIR210HG;
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学科分类号
摘要
Hepatocellular carcinoma (HCC) is a major cause of cancer-related death due to early metastasis or recurrence. Tumor angiogenesis plays an essential role in the tumorigenesis of HCC. Accumulated studies have validated the crucial role of lncRNAs in tumor angiogenesis. Here, we established an angiogenesis-related multi-lncRNAs risk model based on the machine learning for HCC prognosis prediction. Firstly, a total of 348 differential expression angiogenesis-related lncRNAs were identified by correlation analysis. Then, 20 of these lncRNAs were selected through univariate cox analysis and used for in-depth study of machine learning. After 1,000 random sampling cycles calculating by random forest algorithm, four lncRNAs were found to be highly associated with HCC prognosis, namely LUCAT1, AC010761.1, AC006504.7 and MIR210HG. Subsequently, the results from both the training and validation sets revealed that the four lncRNAs-based risk model was suitable for predicting HCC recurrence. Moreover, the infiltration of macrophages and CD8 T cells were shown to be closely associated with risk score and promotion of immune escape. The reliability of this model was validated by exploring the biological functions of lncRNA MIR210HG in HCC cells. The results showed that MIR210HG silence inhibited HCC growth and migration through upregulating PFKFB4 and SPAG4. Taken together, this angiogenesis-related risk model could serve as a reliable and promising tool to predict the prognosis of HCC.
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