Dunk A A, Ikeda T, Pignatelli M, Thomas H C
J Hepatol. 1986;2(3):419-29. doi: 10.1016/s0168-8278(86)80053-8.
We have examined the growth inhibitory effects of human lymphoblastoid interferon (IFN) on the human hepatocellular carcinoma (HCC) cell line PLC/PRF/5. In vitro, PLC/PRF/5 cells were sensitive to the antiproliferative effects of IFN, growth inhibition being noted at concentrations as low as 1.25 i.u. ml-1. Athymic mice with xenografted tumours derived from the PLC/PRF/5 cell line were treated daily with IFN or a saline control. An IFN dose of 2 X 10(5) i.u./day was found capable of significantly slowing tumour growth rate and prolonging mouse survival. Further studies to examine the mechanisms involved in growth inhibition in vivo demonstrated that IFN was capable of inducing the activity of the enzyme 2,5-oligoadenylic acid (2,5 A) synthetase, a potent inhibitor of protein synthesis, in tumour xenografts but not in mouse tissue, and that IFN significantly enhanced the membrane display of HLA class I glycoproteins on tumour cells, though histology did not reveal any increase in tumour infiltration by host lymphocytes. We conclude that IFN exerts potent growth inhibitory effects on the HCC cell line PLC/PRF/5 both in vitro and in vivo and its mode of action in this animal model system appears to be predominantly mediated by a direct antiproliferative effect on tumour cells.
我们研究了人淋巴母细胞干扰素(IFN)对人肝癌(HCC)细胞系PLC/PRF/5的生长抑制作用。在体外,PLC/PRF/5细胞对IFN的抗增殖作用敏感,在低至1.25国际单位/毫升的浓度下即可观察到生长抑制。将源自PLC/PRF/5细胞系的肿瘤移植到裸鼠体内,每天用IFN或生理盐水对照进行处理。发现剂量为2×10⁵国际单位/天的IFN能够显著减缓肿瘤生长速度并延长小鼠存活时间。进一步研究体内生长抑制所涉及的机制表明,IFN能够在肿瘤异种移植物中诱导2,5-寡腺苷酸(2,5A)合成酶的活性,该酶是一种有效的蛋白质合成抑制剂,但在小鼠组织中则不能,并且IFN显著增强了肿瘤细胞上HLA I类糖蛋白的膜表达,尽管组织学检查未发现宿主淋巴细胞对肿瘤浸润有任何增加。我们得出结论,IFN在体外和体内均对HCC细胞系PLC/PRF/5发挥强大的生长抑制作用,在该动物模型系统中其作用模式似乎主要是通过对肿瘤细胞的直接抗增殖作用介导的。