Ishii M, Abe O, Okura H, Okazaki N, Kawai T, Saito Y, Sawabu N, Takamizawa Y, Takeuchi T, Niitani H
Gan To Kagaku Ryoho. 1987 Aug;14(8):2548-55.
The CA-50 enzyme immunoassay kit (EIA kit) that has been developed with the use of C-50 monoclonal antibody prepared by L. Lindholm et al. was evaluated for diagnosis of human cancer. The levels of CA-50 in the sera were determined using this kit supplied from Mitsui Pharmaceuticals, Inc. Co. in 759 healthy donors, 728 patients with benign disease and 1,263 untreated patients with cancer. A CA-50 concentration of 40 U/ml of serum was used as the cut-off value. Patients with pancreatic cancer and patients with bile duct cancer had high positive incidence of 75% and 68%, respectively, compared with a low positive incidence of under 40% in patients with other cancers. On the other hand, positive rates in patients with benign disease were as low as 13%. Comparison of the serum levels of CA-50 with CA19-9 in the same samples did not exhibit complete positive correlation in patients with pancreatic cancer, patients with bile duct cancer and patients with liver cancer. These findings indicated that C-50 antibody reacted with two epitopes of CA19-9 and sialosyllactotetraose. From the above results, the usefulness of CA-50 as a tumor marker for pancreatic cancer and bile duct cancer was recognized with this EIA kit.
利用L. Lindholm等人制备的C - 50单克隆抗体制备的CA - 50酶免疫分析试剂盒(EIA试剂盒)用于人类癌症诊断评估。使用三井制药公司提供的该试剂盒测定了759名健康供体、728名良性疾病患者和1263名未经治疗的癌症患者血清中的CA - 50水平。血清CA - 50浓度40 U/ml用作临界值。胰腺癌患者和胆管癌患者的阳性发生率较高,分别为75%和68%,而其他癌症患者的阳性发生率低于40%。另一方面,良性疾病患者的阳性率低至13%。在相同样本中,胰腺癌患者、胆管癌患者和肝癌患者血清中CA - 50水平与CA19 - 9水平的比较未显示完全正相关。这些发现表明C - 50抗体与CA19 - 9和唾液酸乳糖四糖的两个表位发生反应。根据上述结果,该EIA试剂盒确认了CA - 50作为胰腺癌和胆管癌肿瘤标志物的有用性。