Urine Liquid Biopsies via Highly Integrated Digital PCR System for Accurate Detection of Bladder Cancer

IF 3.7 4区 医学 Q2 PHARMACOLOGY & PHARMACY Advanced Therapeutics Pub Date : 2024-06-17 DOI:10.1002/adtp.202400191
Yue Zhang, Ming Xu, Zhihong Wu, Fan Yang, Lu Zhang, Yiquan Liu, Jiahao Lv, Shuyue Xiang, Beiyuan Fan, Zijian Zhao, Yanzhao Li, Yang Yu
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Abstract

Bladder cancer (BC) is a prevalent urological tumor with high recurrence rates, requiring long-term monitoring. Although cystoscopy is the primary diagnostic method, its invasiveness and cost hinder routine screening and follow-up. This study aimed to develop a novel diagnostic tool utilizing newly developed on-chip heating dPCR platform, which features integrated and rapid temperature control capabilities, for non-invasive BC detection. The dPCR platform is improved by integrating a multi-color detection system, enabling precise quantification of mutant allelic fraction (MAF) of TERT promoter mutations with a limit of detection (LOD) of 0.29%. Diagnostic performance is enhanced by integrating the NRN1 methylation biomarker and employing machine learning to optimize biomarker weighting. Testing the model on urine samples from controls (n = 35) and BC patients (n = 41) yielded a sensitivity of 0.92, specificity of 0.94, and an AUC of 0.98, surpassing conventional cytology in sensitivity while maintaining comparable specificity. Furthermore, the model effectively differentiated between normal controls and different stages, achieving accuracies of 0.92, 0.71, and 0.79 for NC, stage I, and stage II+ respectively. These findings suggest the proposed dPCR assays could serve as a sensitive and non-invasive approach for BC detection in clinical practice.

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通过高度集成的数字 PCR 系统进行尿液液体活检,准确检测膀胱癌
膀胱癌(BC)是一种常见的泌尿系统肿瘤,复发率高,需要长期监测。虽然膀胱镜检查是主要的诊断方法,但其侵入性和成本阻碍了常规筛查和随访。本研究旨在利用新开发的片上加热 dPCR 平台开发一种新型诊断工具,该平台具有集成和快速温控功能,可用于无创膀胱癌检测。该 dPCR 平台通过集成多色检测系统进行了改进,可精确定量 TERT 启动子突变的等位基因突变率 (MAF),检测限 (LOD) 为 0.29%。通过整合 NRN1 甲基化生物标记物和利用机器学习优化生物标记物权重,诊断性能得到了提高。在对照组(35 人)和 BC 患者(41 人)的尿液样本上测试该模型,结果灵敏度为 0.92,特异性为 0.94,AUC 为 0.98,在灵敏度方面超过了传统细胞学,同时保持了相当的特异性。此外,该模型还能有效区分正常对照组和不同分期,NC、I 期和 II+ 期的准确度分别为 0.92、0.71 和 0.79。这些研究结果表明,所提出的 dPCR 检测方法可作为临床实践中检测 BC 的一种灵敏而无创的方法。
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来源期刊
Advanced Therapeutics
Advanced Therapeutics Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
7.10
自引率
2.20%
发文量
130
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