Freeman J W, Busch R K, Gyorkey F, Gyorkey P, Ross B E, Busch H
Department of Pharmacology, Baylor College of Medicine, Houston, Texas 77030.
Cancer Res. 1988 Mar 1;48(5):1244-51.
Tumor nucleoli were treated with polyclonal antisera to normal human tissue nucleoli to block some determinants common to tumor and normal tissue nucleoli. Immunization of mice with these immune complexes resulted in the development of a monoclonal antibody (FB2) to a novel Mr 120,000 nucleolar proliferation-associated antigen. By indirect immunofluorescence, antibody FB2 produced bright nucleolar staining in a variety of malignant tumors, including cancers of the breast, liver, gastrointestinal tract, genitourinary tract, blood, lymph system, lung, and brain. Although specific nucleolar immunofluorescence was not detectable in most normal tissues, it was detectable in some proliferating nonmalignant tissues including spermatogonia of the testes, ductal regions of hypertrophied prostates, and phytohemagglutinin-stimulated lymphocytes. The Mr 120,000 antigen was not detectable in 48-h serum-deprived HeLa cells but was readily detectable (within 30 min) following serum refeeding. The Mr 120,000 antigen was not detected in retinoic acid-treated HL-60 cells following morphological differentiation but was detectable in 48-h phytohemagglutinin-treated lymphocytes. These studies suggest that the Mr 120,000 antigen is a proliferation-associated antigen which plays a role in the early G1 phase of the cell cycle.
用针对正常人组织核仁的多克隆抗血清处理肿瘤核仁,以阻断肿瘤和正常组织核仁共有的一些决定簇。用这些免疫复合物免疫小鼠,产生了一种针对一种新的分子量为120,000的核仁增殖相关抗原的单克隆抗体(FB2)。通过间接免疫荧光法,抗体FB2在多种恶性肿瘤中产生明亮的核仁染色,包括乳腺癌、肝癌、胃肠道癌、泌尿生殖道癌、血液癌、淋巴系统癌、肺癌和脑癌。虽然在大多数正常组织中未检测到特异性核仁免疫荧光,但在一些增殖性非恶性组织中可检测到,包括睾丸精原细胞、肥大前列腺的导管区域以及植物血凝素刺激的淋巴细胞。在血清剥夺48小时的HeLa细胞中未检测到分子量为120,000的抗原,但在重新添加血清后(30分钟内)很容易检测到。在经视黄酸处理的HL-60细胞形态分化后未检测到分子量为120,000的抗原,但在经植物血凝素处理48小时的淋巴细胞中可检测到。这些研究表明,分子量为120,000的抗原是一种增殖相关抗原,在细胞周期的G1早期阶段起作用。