Clark S, McGuckin M A, Hurst T, Ward B G
Department of Obstetrics and Gynaecology, University of Queensland, Royal Brisbane Hospital, Herston, Australia.
Dis Markers. 1994 Oct;12(1):43-50. doi: 10.1155/1994/480236.
In view of the potential uses of cell surface tumour associated antigens in novel anticancer treatment, a study was designed to investigate whether the biological response modifiers interferon-gamma (IFN-gamma) and tumour necrosis factor-alpha (TNF-alpha) could effect the expression of an epitope on the tumour associated MUC1 epithelial mucin. Four ovarian carcinoma cell lines showing high (OAW42 and GG) and low (JAM and PE01) basal expression of MUC1 were treated with 10-1000 U/mL of IFN-gamma or TNF-alpha for one or five days. Changes in MUC1 expression in cells exposed to IFN-gamma or TNF-alpha were monitored using an ELISA technique with the monoclonal antibody BC2 which reacts with a core protein epitope on the MUC1 mucin, and then corrected for the number of viable cells present. TNF-alpha had little effect on MUC1 expression, but one or five days exposure to IFN-gamma significantly increased MUC1 expression (p < 0.01) in all cell lines including the two cell lines that initially showed little or no expression.
鉴于细胞表面肿瘤相关抗原在新型抗癌治疗中的潜在用途,设计了一项研究来调查生物反应调节剂γ干扰素(IFN-γ)和肿瘤坏死因子-α(TNF-α)是否会影响肿瘤相关MUC1上皮粘蛋白上一个表位的表达。用10 - 1000 U/mL的IFN-γ或TNF-α处理四株显示MUC1基础表达高(OAW42和GG)和低(JAM和PE01)的卵巢癌细胞系1天或5天。使用与MUC1粘蛋白上一个核心蛋白表位反应的单克隆抗体BC2,通过ELISA技术监测暴露于IFN-γ或TNF-α的细胞中MUC1表达的变化,然后根据存在的活细胞数量进行校正。TNF-α对MUC1表达影响很小,但在包括最初显示很少或没有表达的两株细胞系在内的所有细胞系中,暴露于IFN-γ 1天或5天均显著增加了MUC1表达(p < 0.01)。