医学
尿
泌尿系统
蛋白质组学
内科学
生物标志物
肿瘤科
恶性肿瘤
癌症
生物信息学
生物
生物化学
基因
作者
Chao‐Jung Chen,Che‐Yi Chou,Kuo-Hsiung Shu,Hung‐Chun Chen,Ming-Cheng Wang,Chia‐Chu Chang,Bang-Gee Hsu,Mai-Szu Wu,Yuan-Lung Yang,Wen‐Ling Liao,Chieh Yang,Yu-Tien Hsiao,Chiu‐Ching Huang
标识
DOI:10.1021/acs.jproteome.1c00164
摘要
Urothelial carcinoma (UC) is the ninth most prevalent malignancy worldwide. Noninvasive and efficient biomarkers with high accuracy are imperative for the surveillance and diagnosis of UC. CKD patients were enrolled as a control group in this study for the discovery of highly specific urinary protein markers of UC. An iTRAQ-labeled quantitative proteomic approach was used to discover novel potential markers. These markers were further validated with 501 samples by ELISA assay, and their diagnostic accuracies were compared to those of other reported UC markers. BRDT, CYBP, GARS, and HDGF were identified as novel urinary UC biomarkers with a high discrimination ability in a population comprising CKD and healthy subjects. The diagnostic values of the four novel UC markers were better than that of a panel of well-known or FDA-approved urinary protein markers CYFR21.1, Midkine, and NUMA1. Three of our discovered markers (BRDT, HDGF, GARS) and one well-known marker (CYFR21.1) were finally selected and combined as a marker panel having AUC values of 0.962 (95% CI, 0.94–0.98) and 0.860 (95% CI, 0.83–0.89) for the discrimination between UC and normal groups and UC and control (healthy + CKD) groups, respectively.
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