Plasma extracellular vesicle circRNA signature and resistance to abiraterone in metastatic castration-resistant prostate cancer

被引:8
|
作者
Tao, Wen [1 ]
Luo, Zi-Huan [1 ]
He, Ya-Di [2 ]
Wang, Bang-Yu [3 ]
Xia, Tao-Lin [4 ]
Deng, Wei-Ming [5 ]
Zhang, Ling-Xiao [6 ]
Tang, Xiu-Mei [2 ]
Meng, Zhan-Ao [7 ]
Gao, Xin [1 ]
Li, Liao-Yuan [1 ]
机构
[1] Sun Yat sen Univ, Affiliated Hosp 3, Dept Urol, Guangzhou 510630, Peoples R China
[2] Sun Yat sen Univ, Affiliated Hosp 3, Ctr Hlth Management, Guangzhou 510630, Peoples R China
[3] Sun Yat sen Univ, Affiliated Hosp 3, Dept Breast Surg, Guangzhou 510630, Peoples R China
[4] Sun Yat sen Univ, Foshan Municipal Peoples Hosp 1, Dept Urol, Foshan 528000, Peoples R China
[5] Univ South China, Affiliated Hosp 1, Dept Urol, Hengyang 421000, Peoples R China
[6] Hainan Med Univ, Affiliated Hosp 1, Dept Urol, Haikou 570102, Peoples R China
[7] Sun Yat sen Univ, Affiliated Hosp 3, Dept Radiol, Guangzhou 510630, Peoples R China
基金
中国国家自然科学基金;
关键词
CIRCULAR RNA; VARIANT; 7; ENZALUTAMIDE; INHIBITOR; BIOMARKER; EXOSOMES; ACETATE; TRIALS; MODEL;
D O I
10.1038/s41416-023-02147-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundWe aimed to develop and validate a plasma extracellular vesicle circular RNA (circRNA)-based signature that can predict overall survival (OS) in first-line abiraterone therapy for metastatic castration-resistant prostate cancer (mCRPC) patients.MethodsIn total, 582 mCRPC patients undergoing first-line abiraterone therapy from four institutions were sorted by three phases. In the discovery phase, 30 plasma samples from 30 case-matched patients with or without early progression were obtained to generate circRNA expression profiles using RNA sequencing. In the training phase, differentially expressed circRNAs were examined using digital droplet PCR in a training cohort (n = 203). The circRNA signature was constructed using a least absolute shrinkage and selection operator Cox regression to predict OS. In the validation phase, the prognostic ability of this signature was prospectively validated in two external cohorts (Cohort I, n = 183; Cohort II, n = 166).ResultsWe developed a five-circRNA signature, based on circCEP112, circFAM13A, circBRWD1, circVPS13C and circMACROD2, which successfully stratified patients into high-risk and low-risk groups. The prognostic ability of this signature was prospectively validated in two external cohorts (P < 0.0001, P < 0.0001). Patients with high-risk scores had shorter OS than patients with low-risk scores.ConclusionThis five-circRNA signature is a reliable predictor of OS for mCRPC patients undergoing abiraterone.
引用
收藏
页码:1320 / 1332
页数:13
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