Kuriyama M
Department of Urology, Gifu University School of Medicine, Japan.
Int J Biol Markers. 1986 May-Aug;1(2):67-76.
Prostate-specific antigen (PA) has been evaluated clinically as a tumor marker of prostate cancer with the use of enzyme immunoassay (EIA). For serodetection of prostate cancer, PA was assayed in a total of 1,109 sera. From mean +/- 3 S.D. of normal controls, upper cut-off values in males were decided as 2.5 and 1.2 ng/ml in Americans and Japanese, respectively. Serum PA values in prostate cancer patients were positive in 78% of Americans and 62% of Japanese. However, in benign prostatic hypertrophy (BPH) cases, a high false positive rate of 41% was observed in Americans. Simultaneous assays of serum PA and PAP showed high sensitivity and specificity in the detection of prostate cancer. This antigen could be used, as well as PAP, for monitoring prostate cancer patients. Furthermore, serum PA levels prior to treatment may express to some degree the malignant potential of the cancer. These results suggest that PA may be useful as a tumor marker of prostate cancer.
前列腺特异性抗原(PA)已通过酶免疫测定法(EIA)作为前列腺癌的肿瘤标志物进行临床评估。为了进行前列腺癌的血清检测,共检测了1109份血清中的PA。根据正常对照的均值±3个标准差,美国男性和日本男性的上限值分别确定为2.5 ng/ml和1.2 ng/ml。前列腺癌患者的血清PA值在美国人为78%呈阳性,在日本人为62%呈阳性。然而,在良性前列腺增生(BPH)病例中,美国人的假阳性率高达41%。血清PA和PAP的同时检测在前列腺癌的检测中显示出高灵敏度和特异性。这种抗原与PAP一样,可用于监测前列腺癌患者。此外,治疗前的血清PA水平可能在一定程度上反映癌症的恶性潜能。这些结果表明,PA可能作为前列腺癌的肿瘤标志物有用。