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CCL18 in a Multiplex Urine-Based Assay for the Detection of Bladder Cancer
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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3357344/ https://www.ncbi.nlm.nih.gov/pubmed/22629457 http://dx.doi.org/10.1371/journal.pone.0037797 |
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author | Urquidi, Virginia Kim, Jeongsoon Chang, Myron Dai, Yunfeng Rosser, Charles J. Goodison, Steve |
author_facet | Urquidi, Virginia Kim, Jeongsoon Chang, Myron Dai, Yunfeng Rosser, Charles J. Goodison, Steve |
author_sort | Urquidi, Virginia |
collection | PubMed |
description | 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 to0.938. 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. |
format | Online Article Text |
id | pubmed-3357344 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-33573442012-05-24 CCL18 in a Multiplex Urine-Based Assay for the Detection of Bladder Cancer Urquidi, Virginia Kim, Jeongsoon Chang, Myron Dai, Yunfeng Rosser, Charles J. Goodison, Steve PLoS One Research Article 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 to0.938. 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. Public Library of Science 2012-05-21 /pmc/articles/PMC3357344/ /pubmed/22629457 http://dx.doi.org/10.1371/journal.pone.0037797 Text en Urquidi et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Urquidi, Virginia Kim, Jeongsoon Chang, Myron Dai, Yunfeng Rosser, Charles J. Goodison, Steve CCL18 in a Multiplex Urine-Based Assay for the Detection of Bladder Cancer |
title | CCL18 in a Multiplex Urine-Based Assay for the Detection of Bladder Cancer |
title_full | CCL18 in a Multiplex Urine-Based Assay for the Detection of Bladder Cancer |
title_fullStr | CCL18 in a Multiplex Urine-Based Assay for the Detection of Bladder Cancer |
title_full_unstemmed | CCL18 in a Multiplex Urine-Based Assay for the Detection of Bladder Cancer |
title_short | CCL18 in a Multiplex Urine-Based Assay for the Detection of Bladder Cancer |
title_sort | ccl18 in a multiplex urine-based assay for the detection of bladder cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3357344/ https://www.ncbi.nlm.nih.gov/pubmed/22629457 http://dx.doi.org/10.1371/journal.pone.0037797 |
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