Discovery of Novel Bladder Cancer Biomarkers by Comparative Urine Proteomics Using iTRAQ Technology

被引:123
作者
Chen, Yi-Ting [1 ]
Chen, Chien-Lun [2 ]
Chen, Hsiao-Wei [1 ]
Chung, Ting [1 ]
Wu, Chih-Ching [1 ,4 ,5 ]
Chen, Chi-De [3 ]
Hsu, Chia-Wei [3 ]
Chen, Meng-Chieh [1 ]
Tsui, Ke-Hung [2 ]
Chang, Phei-Lang [2 ]
Chang, Yu-Sun [1 ,3 ]
Yu, Jau-Song [1 ,3 ]
机构
[1] Chang Gung Univ, Mol Med Res Ctr, Tao Yuan 333, Taiwan
[2] Chang Gung Mem Hosp, Dept Urol, Chang Gung Bioinformat Ctr, Tao Yuan 333, Taiwan
[3] Chang Gung Univ, Colleague Med, Grad Inst Biomed Sci, Tao Yuan 333, Taiwan
[4] Chang Gung Univ, Grad Inst Med Biotechnol, Tao Yuan 333, Taiwan
[5] Chang Gung Univ, Dept Med Biotechnol & Lab Sci, Tao Yuan 333, Taiwan
关键词
urine proteome; iTRAQ; bladder cancer; biomarkers; apolipoprotein; heparin cofactor 2 precursor; peroxiredoxin-2; APOLIPOPROTEIN-A-I; SERUM-LIPIDS; LIQUID-CHROMATOGRAPHY; MOLECULAR BIOMARKERS; PROTEIN BIOMARKERS; POTENTIAL MARKERS; STATISTICAL-MODEL; TUMOR-MARKERS; IDENTIFICATION; CHOLESTEROL;
D O I
10.1021/pr100576x
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A urine sample preparation workflow for the iTRAQ (isobaric tag for relative and absolute quantitation) technique was established. The reproducibility of this platform was evaluated and applied to discover proteins with differential levels between pooled urine samples from nontumor controls and three bladder cancer patient subgroups with different grades/stages (a total of 14 controls and 23 cancer cases in two multiplex iTRAQ runs). Combining the results of two independent clinical sample sets, a total of 638 urine proteins were identified. Among them, 55 proteins consistently showed >2-fold differences in both sample sets. Western blot analyses of individual urine samples confirmed that the levels of apolipoprotein A-I (APOA1), apolipoprotein A-II, heparin cofactor 2 precursor and peroxiredoxin-2 were significantly elevated in bladder cancer urine specimens (n = 25-74). Finally, we quantified APOA1 in a number of urine samples using a commercial ELISA and confirmed again its potential value for diagnosis (n = 126, 94.6% sensitivity and 92.0% specificity at a cutoff value of 11.16 ng/mL) and early detection (n = 71, 83.8% sensitivity and 94.0% specificity). Collectively, our results provide the first iTRAQ-based quantitative profile of bladder cancer urine proteins and represent a valuable resource for the discovery of bladder cancer markers.
引用
收藏
页码:5803 / 5815
页数:13
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