首页> 外国专利> EARLY DETECTION OF PROSTRATE CANCER (CAP) BY DETERMINING A RATIO INVOLVING PROSTRATE SPECIFIC ANTIGEN (PSA) AND HUMAN GLANDULAR KALLIKREIN (HGK-1) CONCENTRATIONS

EARLY DETECTION OF PROSTRATE CANCER (CAP) BY DETERMINING A RATIO INVOLVING PROSTRATE SPECIFIC ANTIGEN (PSA) AND HUMAN GLANDULAR KALLIKREIN (HGK-1) CONCENTRATIONS

机译:通过确定比例涉及的前列腺特异性抗原(PSA)和人类腺样激肽释放酶(HGK-1)浓度来早期检测前列腺癌(CAP)

摘要

The invention relates to a bioaffinity assay of prostate-specific antigen (PSA) comprising the measurement of either the concentration of total PSA (PSA-T), the concentration of free form of PSA (PSA-F) or the concentration of PSA complexed to alpha-1-antichymotrypsin (PSA-ACT), PSA-T being the sum of PSA-F and PSA-ACT. According to the invention, additionally the concentration of human glandular kallikrein (hGK-1) is measured. The concentrations of PSA-T and hGK-1 can be measured in one single assay or in separate assays. The sum of the concentrations of PSA-T and hGK-1 is used to determine the ratio a) PSA-F/(PSA-T+hGK-1) and/or b) PSA-ACT/(PSA-T+hGK-1). Both of these ratios are shown to have clinical utility for the discrimination of prostate cancer and benign prostatic hyperplasia.
机译:本发明涉及前列腺特异性抗原(PSA)的生物亲和力测定,包括测量总PSA的浓度(PSA-T),游离形式的PSA的浓度(PSA-F)或与之复合的PSA的浓度。 α-1-抗胰凝乳蛋白酶(PSA-ACT),PSA-T是PSA-F和PSA-ACT的总和。根据本发明,另外测量人腺激肽释放酶(hGK-1)的浓度。 PSA-T和hGK-1的浓度可以通过一种测定法或单独的测定法进行测定。 PSA-T和hGK-1浓度的总和用于确定比率a)PSA-F /(PSA-T + hGK-1)和/或b)PSA-ACT /(PSA-T + hGK- 1)。这两个比率均显示出对前列腺癌和良性前列腺增生的鉴别具有临床实用性。

著录项

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号