Journal of Practical Hepatology ›› 2022, Vol. 25 ›› Issue (5): 693-697.doi: 10.3969/j.issn.1672-5069.2022.05.022

• Hepatoma • Previous Articles     Next Articles

Systematic analysis of functions of RNA-binding proteins in hepatocellular carcinoma

Wu Tong, Zhang Qiaoli, Qi Xuewei   

  1. Centre of Integrated Chinese and Western Medicine, Ditan Hospital, Capital Medical University, Beijing, China
  • Received:2021-11-17 Online:2022-09-10 Published:2022-09-22

Abstract: Objective Based on the cancer genome atlas (TCGA) database, we conducted a systematic bioinformatics analysis of abnormal cancerous RNA binding proteins (RBPs) in patients with hepatocellular carcinoma (HCC), with the aim of identifying the prognostic markers and potential therapeutic targets. Methods The cancerous and adjacent liver tissue HCC RNA sequencing data was downloaded from TCGA database, and the functional enrichment analysis and visualization of interaction relationships among them were performed. The univariate and multivariate Cox regression analyses were subsequently applied to identify RBPs that were significantly related to the prognosis and a prognostic model was constructed. The predictive performance of the prognostic model was evaluated by survival analysis and receiver operating characteristic (ROC) curve and was verified in the test cohort. The human protein atlas online database was applied to verify the RBP levels in the prognostic model. Results A total of 82 differentially expressed RBPs were identified, including 55 up-regulated and 27 down-regulated (FDR< 0.05 and |log2 FC|>1); the further functional enrichment and interaction analyses showed that the differentially expressed RBPs were mainly related to regulation of mRNA metabolic process, RNA catabolic, mRNA catabolic process, and macromolecule methylation; five RBP genes, e.g., the LIN28B, SMG5, PPARGC1A, LARP1B, and ANG were identified as prognostic-related genes and were used to construct the prognostic model; the predictive ability of the prognostic model was verified in the test cohort; the ROC curve analysis showed that the prognostic model had good sensitivity and specificity; the independent prognostic analysis showed that the risk score could be an independent prognostic factor for patients with HCC. Conclusion The constructed prognostic prediction model by analyzing the differentially expressed RBPs in cancerous tissues in patients with HCC is reliable, which might be served as a prognostic biomarkers and therapeutic targets.

Key words: Hepatocellular carcinoma, RNA-binding proteins, Prognostic model, Prediction, Cancer genome atlas database