Cargando…

Six RNA binding proteins (RBPs) related prognostic model predicts overall survival for clear cell renal cell carcinoma and is associated with immune infiltration

The aim of this article was to construct an accurate prognostic model using RNA-binding proteins (RBPs) to predict overall survival (OS) for patients with clear cell renal cell carcinoma (ccRCC) as well as to reveal its associations with immune infiltration. Expression profiles based on RBPs and cli...

Descripción completa

Detalles Bibliográficos
Autores principales: Xing, Qianwei, Luan, Jiaochen, Liu, Shouyong, Ma, Limin, Wang, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Association of Basic Medical Sciences of Federation of Bosnia and Herzegovina 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9162755/
https://www.ncbi.nlm.nih.gov/pubmed/34420511
http://dx.doi.org/10.17305/bjbms.2021.6097
Descripción
Sumario:The aim of this article was to construct an accurate prognostic model using RNA-binding proteins (RBPs) to predict overall survival (OS) for patients with clear cell renal cell carcinoma (ccRCC) as well as to reveal its associations with immune infiltration. Expression profiles based on RBPs and clinical follow-up parameters were obtained from the Cancer Genome Atlas (TCGA) and the ArrayExpress databases. Through univariate COX and LASSO regression analyses, the RBPs based signature was developed. A total of six RBPs (CLK2, IGF2BP2, RNASE2, EZH2, PABPC1L, and RPL22L1) were eventually used to establish a prognostic signature. Based on this signature, ccRCC patients were classified into high-risk and low-risk subgroups and significant OS was obtained in both the internal and external datasets (p < 0.05). AUCs of its ROC curve were all above 0.70 and this signature was an independent prognostic factor of OS for ccRCC (p < 0.05). Nomograms were also constructed to visualize the relationships among individual predictors and 1-, 3-, and 5-year OS for ccRCC. Furthermore, the established RBPs based signature was strongly related to critical clinicopathologic characteristics such as grade (p = 8.921e−12), stage (p = 1.421e−11), M (p = 1.662e−05), and T stage (p = 7.907e−10). Moreover, 12 kinds of tumor-infiltrating immune cells were significantly linked to high-risk and low-risk groups classified by our constructed model (all p < 0.05). Our study successfully identified six RBPs as a robust prognostic signature in ccRCC by both external and internal verifications. Besides, our established model displayed significant associations with immune infiltration. In addition to original clinical parameters, our findings may further help clinicians in predicting patients’ survival status and creating individualized treatment plans.