Substrate gelatin zymogrophy analysis of matrix metalloproteinase-2 and -9 (gelatinase A and B) in sera from patients with benign and malignant prostate disease

D. Bruzzese
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Abstract

Background: it is widely recognized that the measurement of serum prostate-specific antigen (PSA) levels as a biomarker of prostate cancer is imperfect, in that it can have many false positive elevations attributable to benign hyperplasia and subclinical prostatic inflammation. There is increasing data that support a positive correlation between gelatinases (MMP-2 and MMP-9) activity and tumor cell invasion and tumor aggressiveness. Objectives: we evaluated gelatinolytic activities in the sera of patients with prostate carcinoma (PCa) and benign prostate hyperplasia (BPH) in order to verify whether MMP-2 and MMP-9 might have a potential as non-invasive biomarkers. Methods: by gelatin zymography, we verified MMP activity in a total of 42 patients. Of these, 8 had benign prostate hyperplasia and 34 had carcinoma. A total of 16 normal healthy volunteers with no concomitant illnesses were used as controls. Results: four dominant proteinases were detected migrating at ~ 240, 130, 92 and 72 kDa. The most abundant lytic activity is at 92 kDa (MMP-9); whereas MMP-2 is present in smaller quantities. MMP-9 activity is significantly enhanced in the sera from patients with cancer compared with control individuals (p=0.003). Moreover, MMP-9/MMP-2 ratio was able to discriminate cancer patients from healthy subjects as well as from BPH, and the ROC curve showed that the ratio was a significant predictor for prostate cancer with sensitivity of 80% and specificity of 87%. Discussion: these results suggest that the inexpensive measurement of MMPs in serum may serve as a suitable supplementary tool to distinguish patients with prostate cancer from patients with BPH, and the addition of these enzymes to currently available PSA and/or f-PSA/t-PSA ratio might provide clinicians additional objective information on prostate carcinomas.
良恶性前列腺病患者血清基质金属蛋白酶-2和-9(明胶酶A和B)的明胶酶谱分析
背景:人们普遍认为血清前列腺特异性抗原(PSA)水平作为前列腺癌的生物标志物的测量是不完善的,因为它可能有许多可归因于良性增生和亚临床前列腺炎症的假阳性升高。越来越多的数据支持明胶酶(MMP-2和MMP-9)活性与肿瘤细胞侵袭和肿瘤侵袭性之间的正相关。目的:我们评估前列腺癌(PCa)和良性前列腺增生(BPH)患者血清中的明胶溶解活性,以验证MMP-2和MMP-9是否有可能作为非侵入性生物标志物。方法:采用明胶酶谱法对42例患者的MMP活性进行验证。其中8例为良性前列腺增生,34例为癌。共16名正常健康志愿者,无伴发疾病作为对照。结果:检测到4种优势蛋白酶在~ 240、130、92和72 kDa处迁移。最丰富的裂解活性为92 kDa (MMP-9);而MMP-2的数量较少。与对照组相比,癌症患者血清中MMP-9活性显著增强(p=0.003)。此外,MMP-9/MMP-2比值能够区分癌症患者与健康受试者以及BPH, ROC曲线显示该比值是前列腺癌的显著预测因子,敏感性为80%,特异性为87%。讨论:这些结果表明,血清中MMPs的廉价测量可能作为区分前列腺癌患者和BPH患者的合适补充工具,并且将这些酶添加到目前可用的PSA和/或f-PSA/t-PSA比值中可能为临床医生提供更多关于前列腺癌的客观信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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