A Glycolysis-Related Five-Gene Signature Predicts Biochemical Recurrence-Free Survival in Patients With Prostate Adenocarcinoma

• Published in: Frontiers in oncology Vol. 11; p. 625452
• Main Authors: Xu, Zijun, Xu, Lijuan, Liu, Liping, Li, Hai, Jin, Jiewen, Peng, Miaoguan, Huang, Yanrui, Xiao, Haipeng, Li, Yanbing, Guan, Hongyu
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Media S.A 19.04.2021
• Subjects: biochemical recurrence; gene signature; glycolysis; Oncology; prostate adenocarcinoma; The Cancer Genome Atlas; prostate adenocarcinoma; gene signature; biochemical recurrence; glycolysis; The Cancer Genome Atlas
• ISSN: 2234-943X; 2234-943X
• DOI: 10.3389/fonc.2021.625452

Prostate cancer (PCa) is one of the most frequently diagnosed cancers in males worldwide. Approximately 25% of all patients experience biochemical recurrence (BCR) after radical prostatectomy (RP) and BCR indicates increased risk for metastasis and castration resistance. PCa patients with highly glycolytic tumors have a worse prognosis. Thus, this study aimed to explore glycolysis-based predictive biomarkers for BCR. Expression data and clinical information of PCa samples were retrieved from three publicly available datasets. One from The Cancer Genome Atlas (TCGA) dataset was used as the training cohort, and two from the Gene Expression Omnibus (GEO) dataset (GSE54460 and GSE70769) were used as validation cohorts. Using the training cohort, univariate Cox regression survival analysis, robust likelihood-based survival model, and stepwise multiply Cox analysis were sequentially applied to explore predictive glycolysis-related candidates. A five-gene risk score was then constructed based on the Cox coefficient as the following: (−0.8367*GYS2) + (0.3448*STMN1) + (0.3595*PPFIA4) + (−0.1940*KDELR3) + (0.4779*ABCB6). Receiver operating characteristic curve (ROC) analysis was used to identify the optimal cut-off point, and patients were divided into low risk and high risk groups. Kaplan–Meier analysis revealed that high risk group had significantly shorter BCR free survival time as compared with that in low risk group in training and validation cohorts. In conclusion, our data support the glycolysis-based five-gene signature as a novel and robust signature for predicting BCR of PCa patients.