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The concentration of 12-lipoxygenase in platelet rich plasma as an indication of cancer of the prostate

AIM OF THE STUDY: The aim of this study was to determine whether measuring concentrations of 12-LOX in platelet-rich plasma patients can: 1. Differentiate between the group of patients with prostate cancer and healthy men. 2. Correlate the degree of severity of the disease and the concentration of t...

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Autores principales: Piotrowska, Małgorzata, Szefel, Jarosław, Skrzypczak-Jankun, Ewa, Łysiak-Szydłowska, Wiesława, Szajewski, Mariusz, Aleksandrowicz-Wrona, Ewa, Jankun, Jerzy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3934055/
https://www.ncbi.nlm.nih.gov/pubmed/24592128
http://dx.doi.org/10.5114/wo.2013.37221
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author Piotrowska, Małgorzata
Szefel, Jarosław
Skrzypczak-Jankun, Ewa
Łysiak-Szydłowska, Wiesława
Szajewski, Mariusz
Aleksandrowicz-Wrona, Ewa
Jankun, Jerzy
author_facet Piotrowska, Małgorzata
Szefel, Jarosław
Skrzypczak-Jankun, Ewa
Łysiak-Szydłowska, Wiesława
Szajewski, Mariusz
Aleksandrowicz-Wrona, Ewa
Jankun, Jerzy
author_sort Piotrowska, Małgorzata
collection PubMed
description AIM OF THE STUDY: The aim of this study was to determine whether measuring concentrations of 12-LOX in platelet-rich plasma patients can: 1. Differentiate between the group of patients with prostate cancer and healthy men. 2. Correlate the degree of severity of the disease and the concentration of the enzyme. MATERIAL AND METHODS: The study group comprised 88 men (40–88 years), including 54 patients diagnosed with prostate cancer. The population was divided into 4 groups: group 1 (22 men, aged 55–84 years) –with a negative biopsy, group 2 (36 men, aged 54–88 years) – with a positive biopsy result, group 3 (18 participants aged 58–83) – patients with cancer metastatic disease, group 4 of healthy men (12 people aged 40–66 years) – biopsy was not performed. Routine PSA, morphology and CRP analysis were performed and platelet rich plasma was used for 12(S)LOX determination using an ELISA kit. RESULTS: 1. There was a weak (r = 0.0487) positive correlation between the number of blood platelets and plasma 12(S)LOX. 2. An inverse relationship between 12(S)LOX and Gleason grade was found. 3. Heterogeneity of 12(S)LOX in the group with prostate cancer metastatic disease may suggest differences in the response to the treatment carried out. 4. There were no statistically significant differences in concentrations of 12(S)LOX in different groups of patients. CONCLUSIONS: Our results suggest that 12(S)LOX is relevant in prostate cancer; however, further study should include a larger, more select group of men with prostate cancer.
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spelling pubmed-39340552014-03-03 The concentration of 12-lipoxygenase in platelet rich plasma as an indication of cancer of the prostate Piotrowska, Małgorzata Szefel, Jarosław Skrzypczak-Jankun, Ewa Łysiak-Szydłowska, Wiesława Szajewski, Mariusz Aleksandrowicz-Wrona, Ewa Jankun, Jerzy Contemp Oncol (Pozn) Original Paper AIM OF THE STUDY: The aim of this study was to determine whether measuring concentrations of 12-LOX in platelet-rich plasma patients can: 1. Differentiate between the group of patients with prostate cancer and healthy men. 2. Correlate the degree of severity of the disease and the concentration of the enzyme. MATERIAL AND METHODS: The study group comprised 88 men (40–88 years), including 54 patients diagnosed with prostate cancer. The population was divided into 4 groups: group 1 (22 men, aged 55–84 years) –with a negative biopsy, group 2 (36 men, aged 54–88 years) – with a positive biopsy result, group 3 (18 participants aged 58–83) – patients with cancer metastatic disease, group 4 of healthy men (12 people aged 40–66 years) – biopsy was not performed. Routine PSA, morphology and CRP analysis were performed and platelet rich plasma was used for 12(S)LOX determination using an ELISA kit. RESULTS: 1. There was a weak (r = 0.0487) positive correlation between the number of blood platelets and plasma 12(S)LOX. 2. An inverse relationship between 12(S)LOX and Gleason grade was found. 3. Heterogeneity of 12(S)LOX in the group with prostate cancer metastatic disease may suggest differences in the response to the treatment carried out. 4. There were no statistically significant differences in concentrations of 12(S)LOX in different groups of patients. CONCLUSIONS: Our results suggest that 12(S)LOX is relevant in prostate cancer; however, further study should include a larger, more select group of men with prostate cancer. Termedia Publishing House 2013-10-07 2013 /pmc/articles/PMC3934055/ /pubmed/24592128 http://dx.doi.org/10.5114/wo.2013.37221 Text en Copyright © 2013 Termedia http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Paper
Piotrowska, Małgorzata
Szefel, Jarosław
Skrzypczak-Jankun, Ewa
Łysiak-Szydłowska, Wiesława
Szajewski, Mariusz
Aleksandrowicz-Wrona, Ewa
Jankun, Jerzy
The concentration of 12-lipoxygenase in platelet rich plasma as an indication of cancer of the prostate
title The concentration of 12-lipoxygenase in platelet rich plasma as an indication of cancer of the prostate
title_full The concentration of 12-lipoxygenase in platelet rich plasma as an indication of cancer of the prostate
title_fullStr The concentration of 12-lipoxygenase in platelet rich plasma as an indication of cancer of the prostate
title_full_unstemmed The concentration of 12-lipoxygenase in platelet rich plasma as an indication of cancer of the prostate
title_short The concentration of 12-lipoxygenase in platelet rich plasma as an indication of cancer of the prostate
title_sort concentration of 12-lipoxygenase in platelet rich plasma as an indication of cancer of the prostate
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3934055/
https://www.ncbi.nlm.nih.gov/pubmed/24592128
http://dx.doi.org/10.5114/wo.2013.37221
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