{"title":"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","authors":"D. Bruzzese","doi":"10.11138/PER/2014.3.3.089","DOIUrl":null,"url":null,"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.","PeriodicalId":109386,"journal":{"name":"Prevention and Research","volume":"30 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Substrate gelatin zymogrophy analysis of matrix metalloproteinase-2 and -9 (gelatinase A and B) in sera from patients with benign and malignant prostate disease\",\"authors\":\"D. Bruzzese\",\"doi\":\"10.11138/PER/2014.3.3.089\",\"DOIUrl\":null,\"url\":null,\"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.\",\"PeriodicalId\":109386,\"journal\":{\"name\":\"Prevention and Research\",\"volume\":\"30 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1900-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Prevention and Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.11138/PER/2014.3.3.089\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Prevention and Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.11138/PER/2014.3.3.089","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Substrate gelatin zymogrophy analysis of matrix metalloproteinase-2 and -9 (gelatinase A and B) in sera from patients with benign and malignant prostate disease
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.