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Relationship of urinary isoprostanes to prostate cancer occurence

To estimate the oxidative stress in patients with prostate cancer and in a control group, we used the biomarker of lipid peroxidation–isoprostanes (8-isoPGF(2)) and the level of selected antioxidants (glucose and uric acid [UA]). The level of urinary isoprostanes was determined in patients and contr...

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Autores principales: Brys, Magdalena, Morel, Agnieszka, Forma, Ewa, Krzeslak, Anna, Wilkosz, Jacek, Rozanski, Waldemar, Olas, Beata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3506833/
https://www.ncbi.nlm.nih.gov/pubmed/22983829
http://dx.doi.org/10.1007/s11010-012-1455-z
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author Brys, Magdalena
Morel, Agnieszka
Forma, Ewa
Krzeslak, Anna
Wilkosz, Jacek
Rozanski, Waldemar
Olas, Beata
author_facet Brys, Magdalena
Morel, Agnieszka
Forma, Ewa
Krzeslak, Anna
Wilkosz, Jacek
Rozanski, Waldemar
Olas, Beata
author_sort Brys, Magdalena
collection PubMed
description To estimate the oxidative stress in patients with prostate cancer and in a control group, we used the biomarker of lipid peroxidation–isoprostanes (8-isoPGF(2)) and the level of selected antioxidants (glucose and uric acid [UA]). The level of urinary isoprostanes was determined in patients and controls using an immunoassay kit according to the manufacturer’s instruction. The levels of UA and glucose were also determined in serum by the use of UA Assay Kit and Glucose Assay Kit. We observed a statistically increased the level of isoprostanes in urine of patients with prostate cancer in compared with a control group. The concentration of tested antioxidants in blood from patients with prostate cancer was also higher than in healthy subjects. Moreover, our experiments indicate that the correlation between the increased amount of UA and the lipid peroxidation exists in prostate cancer patients (in all tested groups). Prostate cancer risk by urinary isoprostanes level was analyzed, and a positive association was found (relative risk for highest vs. lowest quartile of urinary isoprostanes = 1.6; 95 % confidence interval 1.2–2.4; p for trend = 0.03). We suggest that reactive oxygen species induce peroxidation of unsaturated fatty acid in patients with prostate cancer, and the level of isoprostanes may be used as a non-invasive marker for determination of oxidative stress. We also propose that UA may enhance the oxidative stress in patients with prostate cancer.
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spelling pubmed-35068332012-11-28 Relationship of urinary isoprostanes to prostate cancer occurence Brys, Magdalena Morel, Agnieszka Forma, Ewa Krzeslak, Anna Wilkosz, Jacek Rozanski, Waldemar Olas, Beata Mol Cell Biochem Article To estimate the oxidative stress in patients with prostate cancer and in a control group, we used the biomarker of lipid peroxidation–isoprostanes (8-isoPGF(2)) and the level of selected antioxidants (glucose and uric acid [UA]). The level of urinary isoprostanes was determined in patients and controls using an immunoassay kit according to the manufacturer’s instruction. The levels of UA and glucose were also determined in serum by the use of UA Assay Kit and Glucose Assay Kit. We observed a statistically increased the level of isoprostanes in urine of patients with prostate cancer in compared with a control group. The concentration of tested antioxidants in blood from patients with prostate cancer was also higher than in healthy subjects. Moreover, our experiments indicate that the correlation between the increased amount of UA and the lipid peroxidation exists in prostate cancer patients (in all tested groups). Prostate cancer risk by urinary isoprostanes level was analyzed, and a positive association was found (relative risk for highest vs. lowest quartile of urinary isoprostanes = 1.6; 95 % confidence interval 1.2–2.4; p for trend = 0.03). We suggest that reactive oxygen species induce peroxidation of unsaturated fatty acid in patients with prostate cancer, and the level of isoprostanes may be used as a non-invasive marker for determination of oxidative stress. We also propose that UA may enhance the oxidative stress in patients with prostate cancer. Springer US 2012-09-16 2013 /pmc/articles/PMC3506833/ /pubmed/22983829 http://dx.doi.org/10.1007/s11010-012-1455-z Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Article
Brys, Magdalena
Morel, Agnieszka
Forma, Ewa
Krzeslak, Anna
Wilkosz, Jacek
Rozanski, Waldemar
Olas, Beata
Relationship of urinary isoprostanes to prostate cancer occurence
title Relationship of urinary isoprostanes to prostate cancer occurence
title_full Relationship of urinary isoprostanes to prostate cancer occurence
title_fullStr Relationship of urinary isoprostanes to prostate cancer occurence
title_full_unstemmed Relationship of urinary isoprostanes to prostate cancer occurence
title_short Relationship of urinary isoprostanes to prostate cancer occurence
title_sort relationship of urinary isoprostanes to prostate cancer occurence
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3506833/
https://www.ncbi.nlm.nih.gov/pubmed/22983829
http://dx.doi.org/10.1007/s11010-012-1455-z
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