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Simultaneous multi-analyte urinary protein assay for bladder cancer detection
BACKGROUND: The ability to accurately measure multiple proteins simultaneously in a single assay has the potential to markedly improve the efficiency of a myriad of clinical assays. Here, we tested the performance of a new, multiplex protein array platform to quantitate three bladder cancer-associat...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4230247/ https://www.ncbi.nlm.nih.gov/pubmed/24684904 http://dx.doi.org/10.1186/1472-6750-14-24 |
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author | Rosser, Charles J Dai, Yunfeng Miyake, Makito Zhang, Ge Goodison, Steve |
author_facet | Rosser, Charles J Dai, Yunfeng Miyake, Makito Zhang, Ge Goodison, Steve |
author_sort | Rosser, Charles J |
collection | PubMed |
description | BACKGROUND: The ability to accurately measure multiple proteins simultaneously in a single assay has the potential to markedly improve the efficiency of a myriad of clinical assays. Here, we tested the performance of a new, multiplex protein array platform to quantitate three bladder cancer-associated proteins in urine samples. The following analytes, interleukin 8 (IL8), matrix metallopeptidase 9 (MMP9), and vascular endothelial growth factor A (VEGFA) were monitored using Q-plex, a customized multiplex ELISA system from Quansys Biosciences, and individual target commercial ELISA kits. The performance of the two approaches was compared by evaluating the diagnostic accuracy of the biomarker assays in samples from a cohort of 73 subjects of known bladder cancer status. RESULTS: The combination biomarker panel analyses revealed an AUROC value of 0.9476 for the Q-plex assay, and 0.9119 for the combination of the single-target ELISA assays. The Q-plex assay achieved an overall diagnostic sensitivity of 0.93 and specificity of 0.81, and the individual target ELISA assays achieved an overall sensitivity of 0.77 and specificity of 0.91. CONCLUSION: Based on these encouraging preliminary data, we believe that the Q-Plex technology is a viable platform that can be exploited as an efficient, highly accurate tool to quantitate multiplex panels of diagnostic proteins in biologic specimens. |
format | Online Article Text |
id | pubmed-4230247 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42302472014-11-14 Simultaneous multi-analyte urinary protein assay for bladder cancer detection Rosser, Charles J Dai, Yunfeng Miyake, Makito Zhang, Ge Goodison, Steve BMC Biotechnol Research Article BACKGROUND: The ability to accurately measure multiple proteins simultaneously in a single assay has the potential to markedly improve the efficiency of a myriad of clinical assays. Here, we tested the performance of a new, multiplex protein array platform to quantitate three bladder cancer-associated proteins in urine samples. The following analytes, interleukin 8 (IL8), matrix metallopeptidase 9 (MMP9), and vascular endothelial growth factor A (VEGFA) were monitored using Q-plex, a customized multiplex ELISA system from Quansys Biosciences, and individual target commercial ELISA kits. The performance of the two approaches was compared by evaluating the diagnostic accuracy of the biomarker assays in samples from a cohort of 73 subjects of known bladder cancer status. RESULTS: The combination biomarker panel analyses revealed an AUROC value of 0.9476 for the Q-plex assay, and 0.9119 for the combination of the single-target ELISA assays. The Q-plex assay achieved an overall diagnostic sensitivity of 0.93 and specificity of 0.81, and the individual target ELISA assays achieved an overall sensitivity of 0.77 and specificity of 0.91. CONCLUSION: Based on these encouraging preliminary data, we believe that the Q-Plex technology is a viable platform that can be exploited as an efficient, highly accurate tool to quantitate multiplex panels of diagnostic proteins in biologic specimens. BioMed Central 2014-04-01 /pmc/articles/PMC4230247/ /pubmed/24684904 http://dx.doi.org/10.1186/1472-6750-14-24 Text en Copyright © 2014 Rosser et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Rosser, Charles J Dai, Yunfeng Miyake, Makito Zhang, Ge Goodison, Steve Simultaneous multi-analyte urinary protein assay for bladder cancer detection |
title | Simultaneous multi-analyte urinary protein assay for bladder cancer detection |
title_full | Simultaneous multi-analyte urinary protein assay for bladder cancer detection |
title_fullStr | Simultaneous multi-analyte urinary protein assay for bladder cancer detection |
title_full_unstemmed | Simultaneous multi-analyte urinary protein assay for bladder cancer detection |
title_short | Simultaneous multi-analyte urinary protein assay for bladder cancer detection |
title_sort | simultaneous multi-analyte urinary protein assay for bladder cancer detection |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4230247/ https://www.ncbi.nlm.nih.gov/pubmed/24684904 http://dx.doi.org/10.1186/1472-6750-14-24 |
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