Hara S, Ishii E, Tanaka S, Yokoyama J, Katsumata K, Fujimoto J, Hata J
Department of Pathology, National Children's Medical Research Centre, Tokyo, Japan.
Br J Cancer. 1989 Dec;60(6):875-9. doi: 10.1038/bjc.1989.383.
We have developed a mouse monoclonal antibody 5C11 (IgG2a) against cell surface antigen of Ewing's sarcoma (ES). 5C11 specifically reacted with ESs but not with other small round cell tumours in childhood, i.e. neuroblastomas, primitive neuroectodermal tumours (PNETs), rhabdomyosarcomas and malignant lymphomas. 5C11 did not react with any other tumours in children except for hepatoblastomas. No reactivity has been identified in normal tissues with the exception of fetal hepatocytes. Immunoelectron microscopically, 5C11 reactive antigen was located on cell membrane of ES cells. Biochemically, 5C11 immunoprecipitated a cell surface protein having molecular weight of 81,000 Da. 5C11 is the first antibody which can clearly distinguish ES from neurogenic tumours, especially from PNETs which were recently reported to have common features to ESs regarding chromosal abnormality and proto-oncogene expression but show evident differentiation into neurogenic direction. The results strongly indicate the usefulness of 5C11 not only for diagnostic purpose when no specific marker is available but also for studying the histogenesis of ES. In addition, no reactivity in normal tissue implies its potential application as a therapeutic reagent when the management of ES patients is still a great problem in clinical field.
我们已经开发出一种针对尤因肉瘤(ES)细胞表面抗原的小鼠单克隆抗体5C11(IgG2a)。5C11能与ES特异性反应,但不与儿童期其他小圆细胞肿瘤反应,即神经母细胞瘤、原始神经外胚层肿瘤(PNETs)、横纹肌肉瘤和恶性淋巴瘤。5C11除了与肝母细胞瘤外,不与儿童期的任何其他肿瘤反应。除了胎儿肝细胞外,在正常组织中未发现反应性。免疫电子显微镜检查显示,5C11反应性抗原位于ES细胞的细胞膜上。生化分析表明,5C11免疫沉淀出一种分子量为81,000 Da的细胞表面蛋白。5C11是第一种能够将ES与神经源性肿瘤,特别是与PNETs明确区分开来的抗体;最近有报道称,PNETs在染色体异常和原癌基因表达方面与ES有共同特征,但显示出明显的向神经源性方向分化。这些结果有力地表明,5C11不仅在没有特异性标志物时可用于诊断,而且对于研究ES的组织发生也很有用。此外,在正常组织中无反应性意味着当ES患者的治疗在临床领域仍然是一个重大问题时,它有可能作为一种治疗试剂应用。