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作 者:张耀光[1] 王建业[1] 齐若梅[3] 张力青[1] 万奔[1] 魏东[1] 朱生才[1] 何美懿[2] 陈仁涉[3] 曾品玲
机构地区:[1]卫生部北京医院泌尿外科,100730 [2]卫生部北京医院检验科,100730 [3]卫生部北京老年医学研究所免疫研究室 [4]北京首都国际机场医院检验科
出 处:《中华老年医学杂志》2011年第4期305-309,共5页Chinese Journal of Geriatrics
摘 要:目的 采用酶联免疫吸附法(ELISA)测定血小板反应素-1(TSP-1),并分析TSP-1对前列腺癌的诊断价值.方法 用ELISA斑点法测定TSP-1,研制了3种具有分离特异抗原功能的试剂,研发了一项具有纯化蛋白能力的技术,解决非特异蛋白的交叉反应问题,建立测定TSP-1的ELISA常规方法.并用该方法测定14例良性前列腺增生和18例前列腺癌患者血清标本的TSP-1.结果 前列腺癌组TSP-1值平均(73.77±12.72)%,前列腺增生组为(121.86±19.47),差异有统计学意义(t=8.44,P<0.01).TSP-1和前列腺特异性抗原(PSA)对前列腺癌诊断的敏感性和特异性分别为92.9%、88.9%和85.7%、66.7%,差异有统计学意义(均P<0.01).TSP-1的受试者工作特征曲线(ROC)曲线下面积为0.9663,PSA的ROC曲线下面积为0.7421,差异有统计学意义(P<0.05).结论 应用ELISA方法测定TSP-1现实可行,TSP-1是一种理想的前列腺癌诊断指标,可能比PSA更能够准确地鉴别良性和恶性前列腺疾病.Objective To use enzyme-linked immunosorbent assay (ELISA) for measuring thrombospondin-1 (TSP-1),and to analyze its diagnostic value for prostatic carcinoma.Methods The possible difficulties and the way to solve the difficulties with ELISA spot were explored first.Three agents which could segregate idio-antigen and one technique which could depurate proteinum were designed and developed.The non-idio- proteinum cross reaction problems were solved and the routine method to measure TSP-1 with ELISA was set up successfully.The serum TSP-1 was measured in 14 patients with benign prostatic hyperplasia (BPH) and 18 patients with prostatic carcinoma.Results The TSP-1 values were (73.77±12.72)% and (121.86±-19.47)% in prostatic carcinoma group and benign prostatic hyperplasia group,respectively (t= 8.44,P〈0.01).The diagnostic sensitivity and specificity of TSP-1 and prostate specific antigen (PSA) for prostatic cancer were 92.7%,88.9% and 85.7%,66.7%,respectively (P〈0.01).The area under the receiver operating characteristic curve (ROC) of TSP-1 and PSA were 0.9663 and 0.7421 (P〈0.05).Conclusions The determination of TSP-1 with ELISA is feasible.TSP-1 is an ideal diagnostic parameter for prostatic carcinoma and it may distinguish BPH from malignant prostatic disease more exactly than PSA.
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