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Investigation of CCL18 and A1AT as potential urinary biomarkers for bladder cancer detection

BACKGROUND: In this study, we further investigated the association of two biomarkers, CCL18 and A1AT, with bladder cancer (BCa) and evaluated the influence of potentially confounding factors in an experimental model. METHODS: In a cohort of 308 subjects (102 with BCa), urinary concentrations of CCL1...

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Autores principales: Miyake, Makito, Ross, Shanti, Lawton, Adrienne, Chang, Myron, Dai, Yunfeng, Mengual, Lourdes, Alcaraz, Antonio, Giacoia, Evan Gomes, Goodison, Steve, Rosser, Charles J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3846766/
https://www.ncbi.nlm.nih.gov/pubmed/24011266
http://dx.doi.org/10.1186/1471-2490-13-42
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author Miyake, Makito
Ross, Shanti
Lawton, Adrienne
Chang, Myron
Dai, Yunfeng
Mengual, Lourdes
Alcaraz, Antonio
Giacoia, Evan Gomes
Goodison, Steve
Rosser, Charles J
author_facet Miyake, Makito
Ross, Shanti
Lawton, Adrienne
Chang, Myron
Dai, Yunfeng
Mengual, Lourdes
Alcaraz, Antonio
Giacoia, Evan Gomes
Goodison, Steve
Rosser, Charles J
author_sort Miyake, Makito
collection PubMed
description BACKGROUND: In this study, we further investigated the association of two biomarkers, CCL18 and A1AT, with bladder cancer (BCa) and evaluated the influence of potentially confounding factors in an experimental model. METHODS: In a cohort of 308 subjects (102 with BCa), urinary concentrations of CCL18 and A1AT were assessed by enzyme-linked immunosorbent assay (ELISA). In an experimental model, benign or cancerous cells, in addition to blood, were added to urines from healthy controls and analyzed by ELISA. Lastly, immunohistochemical staining for CCL18 and A1AT in human bladder tumors was performed. RESULTS: Median urinary protein concentrations of CCL18 (52.84 pg/ml vs. 11.13 pg/ml, p < 0.0001) and A1AT (606.4 ng/ml vs. 120.0 ng/ml, p < 0.0001) were significantly elevated in BCa subjects compared to controls. Furthermore, the addition of whole blood to pooled normal urine resulted in a significant increase in both CCL18 and A1AT. IHC staining of bladder tumors revealed CCL18 immunoreactivity in inflammatory cells only, and there was no significant increase in these immunoreactive cells within benign and cancerous tissue and no association with BCa grade nor stage was noted. A1AT immunoreactivity was observed in the cytoplasm of epithelia cells and intensity of immunostaining increased with tumor grade, but not tumor stage. CONCLUSIONS: Further development of A1AT as a diagnostic biomarker for BCa is warranted.
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spelling pubmed-38467662013-12-03 Investigation of CCL18 and A1AT as potential urinary biomarkers for bladder cancer detection Miyake, Makito Ross, Shanti Lawton, Adrienne Chang, Myron Dai, Yunfeng Mengual, Lourdes Alcaraz, Antonio Giacoia, Evan Gomes Goodison, Steve Rosser, Charles J BMC Urol Research Article BACKGROUND: In this study, we further investigated the association of two biomarkers, CCL18 and A1AT, with bladder cancer (BCa) and evaluated the influence of potentially confounding factors in an experimental model. METHODS: In a cohort of 308 subjects (102 with BCa), urinary concentrations of CCL18 and A1AT were assessed by enzyme-linked immunosorbent assay (ELISA). In an experimental model, benign or cancerous cells, in addition to blood, were added to urines from healthy controls and analyzed by ELISA. Lastly, immunohistochemical staining for CCL18 and A1AT in human bladder tumors was performed. RESULTS: Median urinary protein concentrations of CCL18 (52.84 pg/ml vs. 11.13 pg/ml, p < 0.0001) and A1AT (606.4 ng/ml vs. 120.0 ng/ml, p < 0.0001) were significantly elevated in BCa subjects compared to controls. Furthermore, the addition of whole blood to pooled normal urine resulted in a significant increase in both CCL18 and A1AT. IHC staining of bladder tumors revealed CCL18 immunoreactivity in inflammatory cells only, and there was no significant increase in these immunoreactive cells within benign and cancerous tissue and no association with BCa grade nor stage was noted. A1AT immunoreactivity was observed in the cytoplasm of epithelia cells and intensity of immunostaining increased with tumor grade, but not tumor stage. CONCLUSIONS: Further development of A1AT as a diagnostic biomarker for BCa is warranted. BioMed Central 2013-09-05 /pmc/articles/PMC3846766/ /pubmed/24011266 http://dx.doi.org/10.1186/1471-2490-13-42 Text en Copyright © 2013 Miyake 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 cited. 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
Miyake, Makito
Ross, Shanti
Lawton, Adrienne
Chang, Myron
Dai, Yunfeng
Mengual, Lourdes
Alcaraz, Antonio
Giacoia, Evan Gomes
Goodison, Steve
Rosser, Charles J
Investigation of CCL18 and A1AT as potential urinary biomarkers for bladder cancer detection
title Investigation of CCL18 and A1AT as potential urinary biomarkers for bladder cancer detection
title_full Investigation of CCL18 and A1AT as potential urinary biomarkers for bladder cancer detection
title_fullStr Investigation of CCL18 and A1AT as potential urinary biomarkers for bladder cancer detection
title_full_unstemmed Investigation of CCL18 and A1AT as potential urinary biomarkers for bladder cancer detection
title_short Investigation of CCL18 and A1AT as potential urinary biomarkers for bladder cancer detection
title_sort investigation of ccl18 and a1at as potential urinary biomarkers for bladder cancer detection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3846766/
https://www.ncbi.nlm.nih.gov/pubmed/24011266
http://dx.doi.org/10.1186/1471-2490-13-42
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