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Effect Of Interferon-γ and TNF-α on MUCl MUCIN Expression in Ovarian Carcinoma Cell Lines

机译:干扰素-γ和肿瘤坏死因子-α对卵巢癌细胞株MUC1 MUCIN表达的影响

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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-γ) and tumour necrosis factor-alpha (TNF-α) could effect the expression of an epitope on the tumour associated MUC I epithelial mucin. Four ovarian carcinoma cell lines showing high (OAW42 and GG) and low (JAM and PEO1) basal expression of MUC1 were treated with 10-1000 U/mL of IFN-γor TNF-α for one or five days. Changes in MUC1 expression in cells exposed to IFN-γ or TNF-α 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-α had little effect on MUC1 expression, but one or five days exposure to IFN-γ significantly increased MUC1 expression (p < 0.01) in all cell lines including the two cell lines that initially showed little or no expression.
机译:考虑到细胞表面肿瘤相关抗原在新型抗癌治疗中的潜在用途。一项研究旨在研究生物学应答修饰因子干扰素-γ(IFN-γ)和肿瘤坏死因子-α(TNF-α)是否可以影响与肿瘤相关的MUC I上皮粘蛋白的表位表达。用10-1000 U / mLIFN-γ或TNF-α处理四种MUC1基础表达高(OAW42和GG)和低(JAM和PEO1)的卵巢癌细胞系1或5天。使用ELISA技术,用单克隆抗体BC2与MUC1粘蛋白上的核心蛋白表位反应,监测暴露于IFN-γ或TNF-α的细胞中MUC1表达的变化,然后校正存在的活细胞数。 TNF-α对MUC1表达几乎没有影响,但是暴露于IFN-γ1天或5天后,所有细胞系中MUC1表达均显着增加(p <0.01),包括最初表达很少或没有表达的两种细胞系。

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