| Literature DB >> 32817589 |
Xu Chen1, Jingtong Zhang1, Weimei Ruan2, Ming Huang1, Chanjuan Wang3, Hong Wang2, Zeyu Jiang2, Shaogang Wang4, Zheng Liu4, Chunxiao Liu5, Wanlong Tan6, Jin Yang7, Jiaxin Chen2, Zhiwei Chen2, Xia Li2, Xiaoyu Zhang3, Peng Xu5, Lin Chen7, Ruihui Xie1, Qianghua Zhou1, Shizhong Xu1, Darryl Luke Irwin8, Jian-Bing Fan2,3, Jian Huang1,9,10, Tianxin Lin1,9,10,11.
Abstract
BACKGROUNDCurrent methods for the detection and surveillance of bladder cancer (BCa) are often invasive and/or possess suboptimal sensitivity and specificity, especially in early-stage, minimal, and residual tumors.METHODSWe developed an efficient method, termed utMeMA, for the detection of urine tumor DNA methylation at multiple genomic regions by MassARRAY. We identified the BCa-specific methylation markers by combined analyses of cohorts from Sun Yat-sen Memorial Hospital (SYSMH), The Cancer Genome Atlas (TCGA), and the Gene Expression Omnibus (GEO) database. The BCa diagnostic model was built in a retrospective cohort (n = 313) and validated in a multicenter, prospective cohort (n = 175). The performance of this diagnostic assay was analyzed and compared with urine cytology and FISH.RESULTSWe first discovered 26 significant methylation markers of BCa in combined analyses. We built and validated a 2-marker-based diagnostic model that discriminated among patients with BCa with high accuracy (86.7%), sensitivity (90.0%), and specificity (83.1%). Furthermore, the utMeMA-based assay achieved a great improvement in sensitivity over urine cytology and FISH, especially in the detection of early-stage (stage Ta and low-grade tumor, 64.5% vs. 11.8%, 15.8%), minimal (81.0% vs. 14.8%, 37.9%), residual (93.3% vs. 27.3%, 64.3%), and recurrent (89.5% vs. 31.4%, 52.8%) tumors. The urine diagnostic score from this assay was better associated with tumor malignancy and burden.CONCLUSIONUrine tumor DNA methylation assessment for early diagnosis, minimal, residual tumor detection and surveillance in BCa is a rapid, high-throughput, noninvasive, and promising approach, which may reduce the burden of cystoscopy and blind second surgery.FUNDINGThis study was supported by the National Key Research and Development Program of China and the National Natural Science Foundation of China.Entities:
Keywords: Cancer; Genetics; Molecular diagnosis; Oncology; Urology
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Year: 2020 PMID: 32817589 PMCID: PMC7685755 DOI: 10.1172/JCI139597
Source DB: PubMed Journal: J Clin Invest ISSN: 0021-9738 Impact factor: 14.808