Novelli F, Allione A, Bernabei P, Rigamonti L, Forni G
CNR-Center for Immunogenetics and Experimental Oncology, University of Turin, Italy.
Cancer Detect Prev. 1997;21(2):191-5.
We have previously shown that the contrasting ability of interferon-gamma (IFN-gamma) either to stimulate the proliferation of malignant T cells or to induce their apoptosis is determined by the low and high intensity of IFN-gamma receptor (IFN-gamma R) expression, respectively. High IFN-gamma R expression is a marker for the T cell stress that precedes apoptosis. In this paper, we show that a 12- to 24-h culture of three human malignant T-cell lines displaying distinct differentiation stages (ST4, PF382, and Jurkat) in medium supplemented with four chemotherapy drugs (etoposide, cisplatin, cytarabine, and daunomycin) up-modulates their IFN-gamma R expression followed by their apoptosis after 24-48 h later. Increased IFN-gamma R expression (by at least an order of magnitude) was observed in 30 to 90% of cells during exposure to pharmacologic drug concentrations. Timely combination of chemotherapy drugs with IFN-gamma may thus provide a more effective way of inhibiting the progress of human malignant T cells through synergistic induction of their apoptosis.
我们之前已经表明,干扰素-γ(IFN-γ)刺激恶性T细胞增殖或诱导其凋亡的相反能力,分别由IFN-γ受体(IFN-γR)表达的低强度和高强度所决定。高IFN-γR表达是凋亡前T细胞应激的标志物。在本文中,我们表明,在添加四种化疗药物(依托泊苷、顺铂、阿糖胞苷和柔红霉素)的培养基中,对三种处于不同分化阶段的人恶性T细胞系(ST4、PF382和Jurkat)进行12至24小时培养,会上调它们的IFN-γR表达,随后在24至48小时后发生凋亡。在暴露于药理药物浓度期间,30%至90%的细胞中观察到IFN-γR表达增加(至少一个数量级)。因此,化疗药物与IFN-γ的适时联合使用,可能通过协同诱导人恶性T细胞凋亡,提供一种更有效的抑制其进展的方法。