Abstract
We aimed to construct and validate a prognostic-predicting model of rectum adenocarcinoma (READ) based on RNA-binding protein-related genes (RBPGs) by bioinformatics and statistical analysis. We obtained the expression matrix containing 1542 RBPGs from the RBPDB database through the R package. Then, 126 differentially expressed RBPGs (DE-RBPGs) were obtained by differential expression analysis between groups, among which 63 down-regulated genes and 63 up-regulated genes. Next, Ribonucleoprotein complex biosynthesis and assembly were the primary biological processes (BP) identified by the Gene Ontology (GO) enrichment study, cytoplasmic translation, ncRNA processing, ncRNA and rRNA metabolic process. The functions of cellular components (CC) were closely related to organellar and mitochondrial ribosomes and their subunits, spliceosomal complex, mitochondrial matrix and ribonucleoprotein granule. Then, we put 126 DE-RBPGs into the protein–protein interaction (PPI) network, showing the mutual regulation between each DE-RBPGs. In addition, eight prognostics DE-RBPGs (PDE-RBPGs) were identified by Cox regression analysis, among which DIS3L, EFTUD2, FAM98B, IREB2, NOP58, PDCD7 and STRBP were low-risk PDE-RBPGs (HR less than 1), while GTF3A was a high-risk PDE-RBPG (HR greater than 1). A prognosis model consisting of two PDE-RBPGs (EFTUD2 and FAM98B) was finally optimized. The results of the study of the Receiver Operating Characteristics (ROC) curve and the survival analysis revealed that the prognostic-predicting model constructed by us could accurately predict the grouping and prognosis of READ patients. The above results further elucidated the important molecular functions, key biological pathways and gene (protein) interactions of DE-RBPGs. The prognostic-predicting model constructed by us can accurately predict the patients with READ, which is very valuable as a guide for READ early clinical evaluation and therapy.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
