Department of Cytobiochemistry, Faculty of Biology and Environmental Protection, University of Lodz, Pomorska 141/143, 90-236 Lodz, Poland.
Mol Cell Biochem. 2013 Jan;372(1-2):149-53. doi: 10.1007/s11010-012-1455-z. Epub 2012 Sep 16.
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.
为了评估前列腺癌患者和对照组的氧化应激水平,我们使用了脂质过氧化标志物——异前列腺素(8-isoPGF(2))和选定抗氧化剂(葡萄糖和尿酸[UA])的水平。我们根据制造商的说明,使用免疫测定试剂盒在患者和对照组中测定尿液中的异前列腺素水平。还通过使用 UA 测定试剂盒和葡萄糖测定试剂盒在血清中测定 UA 和葡萄糖的水平。我们观察到与对照组相比,前列腺癌患者尿液中的异前列腺素水平呈统计学增加。前列腺癌患者血液中测试抗氧化剂的浓度也高于健康受试者。此外,我们的实验表明,在前列腺癌患者中存在 UA 增加量与脂质过氧化之间的相关性(在所有测试组中)。分析了尿液异前列腺烷水平的前列腺癌风险,发现存在正相关(尿液异前列腺烷最高与最低四分位的相对风险=1.6;95%置信区间 1.2-2.4;趋势检验 p=0.03)。我们认为活性氧诱导前列腺癌患者不饱和脂肪酸的过氧化,异前列腺烷水平可用作确定氧化应激的非侵入性标志物。我们还提出 UA 可能会增强前列腺癌患者的氧化应激。