Urine-derived exosomal PSMA is a promising diagnostic biomarker for the detection of prostate cancer on initial biopsy

被引:10
|
作者
Wang, Cheng-Bang [1 ,2 ]
Chen, Shao-Hua [1 ,2 ]
Zhao, Lin [3 ]
Jin, Xin [4 ,5 ,6 ]
Chen, Xi [3 ]
Ji, Jin [3 ]
Mo, Zeng-Nan [1 ,2 ]
Wang, Fu-Bo [1 ,2 ]
机构
[1] Guangxi Med Univ, Dept Urol, Affiliated Hosp 1, Nanning, Peoples R China
[2] Guangxi Med Univ, Ctr Genom & Personalized Med, Guangxi Collaborat Innovat Ctr Genom & Personaliz, Guangxi Key Lab Genom & Personalized Med, Nanning, Peoples R China
[3] Second Mil Med Univ, Changhai Hosp, Dept Urol, Shanghai 200433, Peoples R China
[4] Southeast Univ, Zhongda Hosp, Dept Urol, Nanjing 210009, Peoples R China
[5] Southeast Univ, Surg Res Ctr, Inst Urol, Med Sch, Nanjing 210009, Peoples R China
[6] Taizhou Peoples Hosp, Dept Urol, Taizhou 225300, Peoples R China
来源
CLINICAL & TRANSLATIONAL ONCOLOGY | 2023年 / 25卷 / 03期
基金
中国国家自然科学基金;
关键词
Prostate-specific membrane antigen; Diagnostic biomarker; Clinically significant prostate cancer; Urine-derived exosomes; Liquid biopsy; MEMBRANE ANTIGEN-EXPRESSION;
D O I
10.1007/s12094-022-02983-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose It is well-established that the lack of accurate diagnostic modalities for prostate cancer (PCa) leads to overdiagnosis and overtreatments. Accordingly, this study aimed to assess the value of urine-derived exosomal prostate-specific membrane antigen (PSMA) as a biomarker for the diagnosis of PCa and clinically significant prostate cancer (csPCa). Methods A total of 284 urine samples were collected from patients after the digital rectal examination (DRE). Urinary exosomes were extracted using commercial kits, and urine-derived exosomal PSMA was determined via enzyme-linked immunosorbent assay (ELISA). Evaluation of diagnostic accuracy of PSMA was performed via receiver operating characteristic (ROC) analysis, decision curve analysis (DCA), and waterfall plots. Results We found that urine-derived exosomal PSMA was significantly higher in PCa and csPCa than in benign prostatic hyperplasia (BPH) and BPH + non-aggressive prostate cancer (naPCa) groups (P < 0.001). Furthermore, the urine-derived exosome PSMA yielded area under the ROC curve (AUC) values of 0.876 and 0.826 for detecting PCa and csPCa, respectively, suggesting better performance than traditional clinical biomarkers. Besides, when the cutoff value used corresponded to a sensitivity of 95%, urine-derived exosomal PSMA could avoid unnecessary biopsies in 41.2% of cases and missed only 0.7% of csPCa cases. Conclusions Urine-derived exosomal PSMA exhibits a good diagnostic yield for detecting PCa and csPCa. Findings of the present study provide the foothold for future studies on cancer management and research in this patient population.
引用
收藏
页码:758 / 767
页数:10
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