Beaupain R, Martyré M C
Laboratoire d'Immunopharmacologie Exprérimentale, UPR-405 CNRS, Paris, France.
Anticancer Res. 1990 Jul-Aug;10(4):1061-6.
We have studied the short- and long-term effects of human recombinant tumor necrosis factor (TNF) and TNF/recombinant human interferon-gamma (IFN-gamma) mixtures on A549 human lung carcinoma cells maintained in organotypic culture. Continuous treatments with 2 x 10; 2 x 10(2); 2 x 10(3) and 2 x 10(4) U/ml TNF or with mixtures of TNF/IFN-gamma at 2 x 10(2) and 10(3) U/ml, respectively, were administered. Nodule growth, cell proliferation and cell survival were studied. On the 2nd day of treatment with TNF, only the highest dose (2 x 10(4) U/ml) diminished cell proliferation significantly, as measured by tritiated thymidine uptake into DNA. On the 10th day, only the lowest TNF dose (2 x 10 U/ml) induced no significant growth inhibition. Necrosis and nodule disintegration were apparent in the 2 x 10(4) U/ml-treated nodules where DNA synthesis decreased. In this case, using agar cloning assays, no cell survival could be observed. Similar results could be obtained with TNF at low concentration (2 x 10(2) U/ml) in combination with INF-gamma (10(3) U/ml), showing a synergistic effect on inhibition of cell proliferation. In the long-term experiments, with the lower TNF doses, in situ evidence of regrowth was observed (outgrowing zones in the nodules) on about the 40th day of treatment, and nodule recovery was confirmed by the resumption of DNA synthesis measured on the 50th day of treatment. No regrowth, however, occurred when the IFN-gamma/TNF combination was used, and the nodules disintegrated completely on the 35th day of treatment without evidence of any cellular survival.
我们研究了重组人肿瘤坏死因子(TNF)及TNF与重组人干扰素-γ(IFN-γ)混合物对维持在器官型培养中的A549人肺癌细胞的短期和长期影响。分别用2×10、2×10²、2×10³和2×10⁴ U/ml的TNF或2×10²和10³ U/ml的TNF/IFN-γ混合物进行持续处理。研究了结节生长、细胞增殖和细胞存活情况。在用TNF处理的第2天,只有最高剂量(2×10⁴ U/ml)能显著降低细胞增殖,这通过氚标记胸腺嘧啶掺入DNA来测定。在第10天,只有最低的TNF剂量(2×10 U/ml)未诱导出明显的生长抑制。在DNA合成减少的2×10⁴ U/ml处理的结节中,坏死和结节崩解明显。在这种情况下,使用琼脂克隆试验,未观察到细胞存活。低浓度(2×10² U/ml)的TNF与INF-γ(10³ U/ml)联合使用可获得类似结果,显示出对细胞增殖抑制的协同作用。在长期实验中,使用较低的TNF剂量时,在处理约第40天时观察到原位再生长的证据(结节中的生长区域),并且通过处理第50天时DNA合成的恢复证实了结节的恢复。然而,当使用IFN-γ/TNF组合时未发生再生长,并且在处理第35天时结节完全崩解,没有任何细胞存活的证据。