Identification of a novel PANoptosis-related gene signature for predicting the prognosis in clear cell renal cell carcinoma

被引:0
|
作者
Yue, Dezhi [1 ]
Ren, Congzhe [1 ]
Li, Hu [2 ]
Liu, Xiaoqiang [1 ]
机构
[1] Tianjin Med Univ, Gen Hosp, Dept Urol, Tianjin 300000, Peoples R China
[2] Shanxian Cent Hosp, Dept Urol, Heze, Shandong, Peoples R China
关键词
clear cell renal cell carcinoma; nomogram; PANoptosis; risk score; signature; CANCER; NECROPTOSIS; APOPTOSIS; PROLIFERATION; INFLAMMASOME; PYROPTOSIS; CASPASE-8;
D O I
10.1097/MD.0000000000039874
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
PANoptosis has been shown to play an important role in tumorigenesis and gain more attention. Yet, the prognostic significance of PANoptosis-related genes has not been investigated more in clear cell renal cell carcinoma (ccRCC). The aim of this research was designed to identify and create a signature of PANoptosis-related genes which was expected to predict prognosis of ccRCC more effectively. The transcriptome data and clinical information were collected from The Cancer Genome Atlas database and the Gene Expression Omnibus database. Optimal differentially expressed PANoptosis-related genes, which were closely associated with prognosis and employed to construct a risk score, were extracted by univariate Cox analysis, least absolute shrinkage and selection operator Cox regression and multivariate Cox analysis. We performed Kaplan-Meier survival analysis and time-dependent receiver operating characteristic curves to complete this process. By adopting univariate and multivariate analysis, the constructed risk score was assessed to verify whether it could be taken as an independent contributor for prognosis. Moreover, we created a nomogram in order to predict overall survival (OS) of ccRCC. Five differentially expressed PANoptosis-related genes were screened out and used to construct a risk score. Our results showed that ccRCC patients with high risk score had a poor prognosis and shorter OS. The results of Kaplan-Meier curves and the area under the receiver operating characteristic curves of 1-, 3-, and 5-year OS indicated that the prediction performance was satisfactory. Additionally, the risk model could be taken as an independent prognostic factor in training and validation cohorts. The nomogram exhibited excellent reliability in predicting OS, which was validated by calibration curves. We identified 5 PANoptosis-related genes, which were used to construct a risk score and a nomogram for prognostic prediction with reliable predictive capability. The present study may provide new potential therapeutic targets and precise treatment strategies for ccRCC.
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页数:15
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