CCL18 in a Multiplex Urine-Based Assay for the Detection of Bladder Cancer

• Published in: PloS one Vol. 7; no. 5; p. e37797
• Main Authors: Urquidi, Virginia, Kim, Jeongsoon, Chang, Myron, Dai, Yunfeng, Rosser, Charles J., Goodison, Steve
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 21.05.2012; Public Library of Science (PLoS)
• Subjects: Accuracy; Adult; Aged; Assaying; Biology; Biomarkers; Biomarkers, Tumor - urine; Bladder; Bladder cancer; Cancer; Cancer diagnosis; Cancer research; Case-Control Studies; CCL18 protein; CD44 antigen; Cellular biology; Chemokines, CC - urine; Comparative analysis; Confidence intervals; Cytology; Early Detection of Cancer - methods; Enzyme-linked immunosorbent assay; Enzymes; Female; Humans; Hyaluronan Receptors - urine; Male; Medical diagnosis; Medical research; Medicine; Middle Aged; Multiplexing; Plasminogen Activator Inhibitor 1 - urine; Plasminogen activator inhibitors; Polyamide-imides; Proteins; Proteomics; Regression analysis; Sensitivity and Specificity; Statistical analysis; Studies; Tumors; Urinary bladder; Urinary Bladder Neoplasms - diagnosis; Urinary Bladder Neoplasms - urine; Urine; Florida; United States > US
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0037797

The early detection of bladder cancer (BCa) is pivotal for successful patient treatment and management. Through genomic and proteomic studies, we have identified a number of bladder cancer-associated biomarkers that have potential clinical utility. In a case-control study, we examined voided urines from 127 subjects: 64 tumor-bearing subjects and 63 controls. The urine concentrations of the following proteins were assessed by enzyme-linked immunosorbent assay (ELISA); C-C motif chemokine 18 (CCL18), Plasminogen Activator Inhibitor 1 (PAI-1) and CD44. Data were compared to a commercial ELISA-based BCa detection assay (BTA-Trak©) and voided urinary cytology. We used analysis of the area under the curve of receiver operating characteristic curves to compare the ability of CCL18, PAI-1, CD44, and BTA to detect BCa in voided urine samples. Urinary concentrations of CCL18, PAI-1, and BTA were significantly elevated in subjects with BCa. CCL18 was the most accurate biomarker (AUC; 0.919; 95% confidence interval [CI], 0.8704-0.9674). Multivariate regression analysis highlighted CCL18 (OR; 18.31; 95% CI, 4.95-67.70, p<0.0001) and BTA (OR; 6.43; 95% CI, 1.86-22.21, p = 0.0033) as independent predictors of BCa in voided urine samples. The combination of CCL18, PAI-1 and CD44 improved the area under the curve to 0.938. Preliminary results indicate that CCL18 was a highly accurate biomarker for BCa detection in this cohort. Monitoring CCL18 in voided urine samples has the potential to improve non-invasive tests for BCa diagnosis. Furthermore using the combination of CCL18, PAI-1 and CD44 may make the model more robust to errors to detect BCa over the individual biomarkers or BTA.