Prognostic Value of an Immune Long Non-Coding RNA Signature in Liver Hepatocellular Carcinoma

被引:1
作者
Kong, Rui [1 ]
Wang, Nan [3 ]
Zhou, Chun li [1 ]
Lu, Jie [2 ,3 ]
机构
[1] Nanjing Med Univ, Affiliated Suzhou Hosp, Suzhou Municipal Hosp, Gusu Sch,Dept Gastroenterol, Nanjing, Peoples R China
[2] Shanghai Univ, Pu Dong Area Gongli Hosp, Sch Med, Dept Gastroenterol, Shanghai 200135, Peoples R China
[3] Shanghai Jiao Tong Univ, Sch Med, Shanghai Gen Hosp, Dept Gastroenterol, Shanghai 200080, Peoples R China
关键词
Long non -coding RNA; immune prognostic signature; hepatocellular carcinoma; overall survival; CANCER; PROLIFERATION; IMMUNOTHERAPY; BIOMARKERS; EXPRESSION; CELLS;
D O I
10.4014/jmb.2308.08022
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
In recent years, there has been a growing recognition of the important role that long non -coding RNAs (lncRNAs) play in the immunological process of hepatocellular carcinoma (LIHC). An increasing number of studies have shown that certain lncRNAs hold great potential as viable options for diagnosis and treatment in clinical practice. The primary objective of our investigation was to devise an immune lncRNA profile to explore the significance of immune -associated lncRNAs in the accurate diagnosis and prognosis of LIHC. Gene expression profiles of LIHC samples obtained from TCGA database were screened for immune -related genes. The optimal immune -related lncRNA signature was built via correlational analysis, univariate and multivariate Cox analysis. Then, the Kaplan -Meier plot, ROC curve, clinical analysis, gene set enrichment analysis, and principal component analysis were performed to evaluate the capability of the immune lncRNA signature as a prognostic indicator. Six long non -coding RNAs were identified via correlation analysis and Cox regression analysis considering their interactions with immune genes. Subsequently, tumor samples were categorized into two distinct risk groups based on different clinical outcomes. Stratification analysis indicated that the prognostic ability of this signature acted as an independent factor. The KaplanMeier method was employed to conduct survival analysis, results showed a significant difference between the two risk groups. The predictive performance of this signature was validated by principal component analysis (PCA). Additionally, data obtained from gene set enrichment analysis (GSEA) revealed several potential biological processes in which these biomarkers may be involved. To summarize, this study demonstrated that this six-lncRNA signature could be identified as a potential factor that can independently predict the prognosis of LIHC patients.
引用
收藏
页码:958 / 968
页数:11
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