A urine extracellular vesicle circRNA classifier for detection of high-grade prostate cancer in patients with prostate-specific antigen 2–10 ng/mL at initial biopsy

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作者
Ya-Di He
Wen Tao
Tao He
Bang-Yu Wang
Xiu-Mei Tang
Liang-Ming Zhang
Zhen-Quan Wu
Wei-Ming Deng
Ling-Xiao Zhang
Chun-Kui Shao
Jing Zhou
Li-Min Rong
Xin Gao
Liao-Yuan Li
机构
[1] Sun Yat-Sen University,Centre of Physical Examination, The Third Affiliated Hospital
[2] Sun Yat-Sen University,Department of Urology, The Third Affiliated Hospital
[3] Sun Yat-Sen University,Breast Surgery, The Third Affiliated Hospital
[4] Sun Yat-Sen University,Department of Spine Surgery, The Third Affiliated Hospital
[5] Sun Yat-Sen University,Department of Urology, Foshan First Municipal People’s Hospital
[6] University of South China,Department of Urology, The First Affiliated Hospital
[7] Hainan Medical College,Department of Urology, The First Affiliated Hospital
[8] Sun Yat-Sen University,Department of Pathology, The Third Affiliated Hospital
来源
Molecular Cancer | / 20卷
关键词
Prostate cancer; Circular RNA (circRNA); Diagnosis; Urine; Extracellular vesicle;
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摘要
The aim of this study was to identify a urine extracellular vesicle circular RNA (circRNA) classifier that could detect high-grade prostate cancer (PCa) of Grade Group (GG) 2 or greater. For this purpose, we used RNA sequencing to identify candidate circRNAs from urinary extracellular vesicles from 11 patients with high-grade PCa and 11 case-matched patients with benign prostatic hyperplasia. Using ddPCR in a training cohort (n = 263), we built a urine extracellular vesicle circRNA classifier (Ccirc, containing circPDLIM5, circSCAF8, circPLXDC2, circSCAMP1, and circCCNT2), which was evaluated in two independent cohorts (n = 497, n = 505). Ccirc showed higher accuracy than two standard of care risk calculators (RCs) (PCPT-RC 2.0 and ERSPC-RC) in both the training cohort and the validation cohorts. In all three cohorts, this novel urine extracellular vesicle circRNA classifier plus RCs was statistically more predictive than RCs alone for predicting ≥ GG2 PCa. This assay, which does not require precollection digital rectal examination nor special handling, is repeatable, noninvasive, and can be easily implemented as part of the basic clinical workflow.
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