Parsons R G, Aldenderfer P H, Kowal R
J Natl Cancer Inst. 1979 Jul;63(1):43-7.
Human serum DNA-binding proteins were fractionated by DNA-cellulose affinity chromatography. Electrophoretic resolution of these protein fractions allowed the direct comparison of DNA-binding proteins from pools of serum from cancer patients, fetuses, or normal humans. A protein band detected in the fraction eluted by 0.6 M NaCl was elevated in pooled cancer serum, compared to normal or fetal serum. This malignant disease-associated DNA-binding protein (MAD-2) did not react with a variety of antisera directed against specific human serum proteins, blood components, or tumor markers. A chromatography-electrophoresis assay system for MAD-2 that allows the simultaneous determination of 20-30 serum samples was developed. This assay system was used for a preliminary clinical study, which revealed elevated MAD-2 levels in sera from pregnant women and individuals with various carcinomas, compared to levels in sera obtained from normal individuals, patients with nonmalignant diseases, or fetal cord samples.
通过DNA - 纤维素亲和色谱法对人血清DNA结合蛋白进行分级分离。对这些蛋白级分进行电泳分离,可直接比较癌症患者、胎儿或正常人血清池中的DNA结合蛋白。与正常或胎儿血清相比,在0.6M NaCl洗脱级分中检测到的一条蛋白带在合并的癌症血清中有所升高。这种与恶性疾病相关的DNA结合蛋白(MAD - 2)不与多种针对特定人血清蛋白、血液成分或肿瘤标志物的抗血清发生反应。开发了一种用于MAD - 2的色谱 - 电泳分析系统,该系统可同时测定20 - 30份血清样本。该分析系统用于一项初步临床研究,结果显示,与正常个体、非恶性疾病患者或胎儿脐带样本的血清水平相比,孕妇和各种癌症患者血清中的MAD - 2水平升高。