Research Paper Volume 15, Issue 13 pp 6445—6466

A novel cuproptosis-related lncRNAs signature predicts prognosis in bladder cancer

Lingfeng Wu1, , Wei Chen1, , Yifang Cao1, , Bin Chen1, , Yi He1, , Xueping Wang1, ,

  • 1 Department of Urology, The Affiliated Hospital of Jiaxing University, Jiaxing, Jiangzhe 314000, China

Received: March 11, 2023       Accepted: June 14, 2023       Published: July 9, 2023      

https://doi.org/10.18632/aging.204861
How to Cite

Copyright: © 2023 Wu et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

This study constructed a novel cuproptosis-related lncRNAs signature to predict the prognosis of BLCA patients. The Cancer Genome Atlas (TCGA) database was used to retrieve the RNA-seq data together with the relevant clinical information. The cuproptosis-related genes were first discovered. The cuproptosis-related lncRNAs were then acquired by univariate, the least absolute shrinkage and selection operator (LASSO) and multivariate Cox regression analysis to create a predictive signature. An eight cuproptosis-related lncRNAs (AC005261.1, AC008074.2, AC021321.1, AL024508.2, AL354919.2, ARHGAP5-AS1, LINC01106, LINC02446) predictive signature was created. Compared with the low-risk group, the prognosis was poorer for the high-risk group. The signature served as an independent overall survival (OS) predictor. Receiver operating characteristic (ROC) curve indicated that the signature demonstrated superior predictive ability, as evidenced by the area under the curve (AUC) of 0.782 than the clinicopathological variables. When we performed a subgroup analysis of the different variables, the high-risk group’s OS for BLCA patients was lower than that of the low-risk group’s patients. Gene Set Enrichment Analysis (GSEA) showed that high-risk groups were clearly enriched in many immune-related biological processes and tumor-related signaling pathways. Single sample gene set enrichment analysis (ssGSEA) revealed that the immune infiltration level was different between the two groups. Finally, quantitative RT-PCR showed that AC005261.1, AC021321.1, AL024508.2, LINC02446 and LINC01106 were lowly expressed in tumor cells, while ARHGAP5-AS1 showed the opposite trend. In summary, the predictive signature can independently predict the prognosis and provide clinical treatment guidance for BLCA patients.

Abbreviations

BLCA: Bladder Urothelial Carcinoma; NMIBC: non-muscle invasive bladder cancer; MIBC: muscle invasive bladder cancer; TCA: tricarboxylic acid; LncRNAs: Long non-coding RNAs; TCGA: The Cancer Genome Atlas; LASSO: the least absolute shrinkage and selection operator; PPI: the protein-protein interaction; OS: overall survival; GSEA: Gene Set Enrichment Analysis; ssGSEA: Single sample gene set enrichment analysis; ROC: receiver operating characteristic; AUC: area under the curve; TNM: Tumor Node Metastasis; PCA: Principal component analysis; CRGs: cuproptosis-related genes.