Marth C, Müller-Holzner E, Gaugg I, Daxenbichler G, Dapunt O
Department of Obstetrics and Gynecology, Innsbruck University Clinic, Austria.
Oncology. 1992;49(1):53-7. doi: 10.1159/000227011.
Interferons are known to modulate several cellular functions by the induction of different proteins. In our study interferon-gamma and -alpha augmented presentation of one specific ovarian cancer antigen recognized by the antibody OV632 on the cell surface on one of four ovarian carcinoma cell lines in vitro (HTB-77). The interferon-gamma effect reached a maximum after 24 of treatment. Both HLA-DR and OV632 antigen expression were increased by interferon-gamma on HTB-77 cells whereas the two cell lines OVCAR-3 and 2780, which respond to an interferon-gamma treatment with a reduced proliferation and induction of HLA-DR, and also the interferon-resistant CRL-1572 were found to be resistant regarding OV632 epitope modulation. The demonstration of OV632 expression provides an important insight into the potential regulatory mechanism governing this tumor marker.
已知干扰素可通过诱导不同蛋白质来调节多种细胞功能。在我们的研究中,γ干扰素和α干扰素增强了一种特定卵巢癌抗原的呈递,该抗原可被抗体OV632在体外的四种卵巢癌细胞系之一(HTB - 77)的细胞表面识别。γ干扰素的作用在处理24小时后达到最大值。在HTB - 77细胞上,γ干扰素使HLA - DR和OV632抗原表达均增加,而OVCAR - 3和2780这两种细胞系在用γ干扰素处理后增殖减少且HLA - DR诱导增加,还有对干扰素耐药的CRL - 1572细胞系,在OV632表位调节方面均表现出耐药性。OV632表达的证明为调控这种肿瘤标志物的潜在调节机制提供了重要见解。