Schiller J H, Bittner G, Storer B, Willson J K
Cancer Res. 1987 Jun 1;47(11):2809-13.
We assessed the antiproliferative effects of tumor necrosis factor (TNF-alpha) and gamma-interferon (IFN-gamma) alone and in combination, on nine human colon carcinoma cell lines. All were resistant (less than 30% inhibition) to TNF-alpha alone. Four cell lines were resistant to IFN-gamma alone, two exhibited a minimal degree of sensitivity (30-50% inhibition), one was moderately sensitive, and two were inhibited 70% or greater. A synergistic antiproliferative effect occurred in eight of the nine cell lines treated with a combination of TNF-alpha and IFN-gamma. In seven of these eight, the combination of cytokines resulted in 30-40% more growth inhibition than predicted had an additive interaction occurred (P less than 0.005). In two cell lines with an induced resistance to mitomycin C, an increase in resistance to combined TNF-alpha and IFN-gamma treatment correlated with an increasing resistance to mitomycin C. The data were further analyzed to determine if combination treatment altered the sensitivity of the cells to one or both agents in addition to synergistically potentiating growth inhibitory effects. Combinations of TNF-alpha/IFN-gamma enhanced the dose response activity of TNF-alpha in three cell lines (P less than or equal to 0.09) and decreased the dose response activity of IFN-gamma in another three (P less than or equal to 0.02). Colony forming experiments on HCT 116 cells demonstrated a reduction in the number of 250-micron colonies in the IFN-gamma/TNF-alpha treatment groups when compared to controls, indicating that combined treatment had a cytotoxic effect. We conclude that combination TNF-alpha/IFN-gamma treatment has a synergistic cytotoxic effect on human colon carcinoma cells. IFN-gamma may enhance the effectiveness of TNF-alpha in some cell lines, but not conversely. These results may have therapeutic implications.
我们评估了肿瘤坏死因子(TNF-α)和γ-干扰素(IFN-γ)单独及联合使用时对九种人结肠癌细胞系的抗增殖作用。所有细胞系对单独使用的TNF-α均有抗性(抑制率低于30%)。四种细胞系对单独使用的IFN-γ有抗性,两种表现出最低程度的敏感性(抑制率30%-50%),一种中度敏感,两种的抑制率达70%或更高。在使用TNF-α和IFN-γ联合处理的九种细胞系中,有八种出现了协同抗增殖作用。在这八种中的七种中,细胞因子联合使用所导致的生长抑制比假设发生相加相互作用时预测的多30%-40%(P<0.005)。在两种对丝裂霉素C诱导产生抗性的细胞系中,对TNF-α和IFN-γ联合处理的抗性增加与对丝裂霉素C的抗性增加相关。对数据进一步分析以确定联合处理除了协同增强生长抑制作用外,是否还改变了细胞对一种或两种药物的敏感性。TNF-α/IFN-γ联合使用增强了三种细胞系中TNF-α的剂量反应活性(P≤0.09),并降低了另外三种细胞系中IFN-γ的剂量反应活性(P≤0.02)。对HCT 116细胞进行的集落形成实验表明,与对照组相比,IFN-γ/TNF-α处理组中250微米集落的数量减少,表明联合处理具有细胞毒性作用。我们得出结论,TNF-α/IFN-γ联合处理对人结肠癌细胞具有协同细胞毒性作用。IFN-γ可能在某些细胞系中增强TNF-α的有效性,但反之则不然。这些结果可能具有治疗意义。