A urine extracellular vesicle lncRNA classifier for high-grade prostate cancer and increased risk of progression: A multi-center study

被引:7
作者
Tao, Wen [1 ]
Wang, Bang-Yu [2 ]
Luo, Liang [1 ]
Li, Qing [3 ]
Meng, Zhan-Ao [4 ]
Xia, Tao-Lin [5 ]
Deng, Wei-Ming [6 ]
Yang, Ming [7 ]
Zhou, Jing [8 ]
Zhang, Xin [9 ]
Gao, Xin [1 ]
Li, Liao-Yuan [1 ]
He, Ya-Di [10 ]
机构
[1] Sun Yat Sen Univ, Affiliated Hosp 3, Dept Urol, Guangzhou 510630, Peoples R China
[2] Shanghai Jiao Tong Univ, Shanghai Gen Hosp, Dept Hematol, Sch Med, Shanghai, Shanghai, Peoples R China
[3] Chinese Univ Hong Kong, Sch Life Sci, Fac Sci, Hong Kong 999077, Peoples R China
[4] Sun Yat Sen Univ, Affiliated Hosp 3, Dept Radiol, Guangzhou 510630, Peoples R China
[5] Sun Yat Sen Univ, Foshan Municipal Peoples Hosp 1, Dept Urol, Foshan 528000, Peoples R China
[6] Univ South China, Affiliated Hosp 1, Dept Urol, Hengyang 421000, Hunan, Peoples R China
[7] Foshan Hosp Tradit Chinese Med, Dept Urol, Foshan 528000, Guangdong, Peoples R China
[8] Sun Yat sen Univ, Affiliated Hosp 3, Dept Gastroenterol, Guangzhou 510630, Peoples R China
[9] Sun Yat Sen Univ, Foshan Municipal Peoples Hosp 1, Dept Urol, Foshan 528000, Peoples R China
[10] Sun Yat Sen Univ, Affiliated Hosp 3, Hlth Management Ctr, Guangzhou 510630, Peoples R China
基金
中国国家自然科学基金;
关键词
RNA; PREDICTION; BIOMARKERS; INDEX; TRANSCRIPTOME; EXOSOMES; MEN;
D O I
10.1016/j.xcrm.2023.101240
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
To construct a urine extracellular vesicle long non-coding RNA (lncRNA) classifier that can detect high-grade prostate cancer (PCa) of grade group 2 or greater and estimate the risk of progression during active surveillance, we identify high-grade PCa-specific lncRNAs by combined analyses of cohorts from TAHSY, TCGA, and the GEO database. We develop and validate a 3-lncRNA diagnostic model (Clnc, being made of AC015987.1, CTD-2589M5.4, RP11-363E6.3) that can detect high-grade PCa. Clnc shows higher accuracy than prostate cancer antigen 3 (PCA3), multiparametric magnetic resonance imaging (mpMRI), and two risk calculators (Prostate Cancer Prevention Trial [PCPT]-RC 2.0 and European Randomized Study of Screening for Prostate Cancer [ERSPC]-RC) in the training cohort (n = 350), two independent cohorts (n = 232; n = 251), and TCGA cohort (n = 499). In the prospective active surveillance cohort (n = 182), Clnc at diagnosis remains a powerful independent predictor for overall active surveillance progression. Thus, Clnc is a potential biomarker for high-grade PCa and can also serve as a biomarker for improved selection of candidates for active surveillance.
引用
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页数:16
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