Chakravarthy A, Pollak M, Hamburger A W
Department of Pathology, University of Maryland, Baltimore 21201.
J Interferon Res. 1991 Feb;11(1):1-8. doi: 10.1089/jir.1991.11.1.
We have determined that interferon-alpha (IFN-alpha) and IFN-gamma inhibit the growth of a human breast tumor cell line, S4, in vitro. Cells were more sensitive to the antiproliferative effects of low-dose IFN-gamma than IFN-alpha. As the growth of the S4 cell line is enhanced by epidermal growth factor (EGF), we examined the effect of IFN on EGF-dependent growth of S4 cells. Cells plated in 2.5% serum alone failed to grow. EGF stimulated these cells to grow more than twofold. IFN substantially attenuated the EGF-stimulated growth of S4 cells. Binding of EGF to its receptor was unaffected by pretreatment of cells with IFN-alpha. However, a 24-h exposure of cells to IFN-gamma significantly increased the number of EGF receptors on S4 cells. Internalization of the EGF receptor was unaffected by IFN treatment. Binding remained elevated through 4 days of IFN-gamma exposure. Scatchard analysis of receptor binding data revealed that IFN-gamma increased the number of binding sites without changing the affinity of the receptor for its ligand. These results demonstrate that IFN inhibits EGF-stimulated growth of a breast tumor cell line and suggest that the antiproliferative effect of IFN may be due, in part, to its interaction with growth factor-initiated pathways.
我们已确定,α干扰素(IFN-α)和γ干扰素在体外可抑制人乳腺癌细胞系S4的生长。细胞对低剂量γ干扰素的抗增殖作用比α干扰素更敏感。由于表皮生长因子(EGF)可促进S4细胞系的生长,我们研究了干扰素对S4细胞依赖EGF的生长的影响。单独接种于2.5%血清中的细胞无法生长。EGF刺激这些细胞生长超过两倍。干扰素显著减弱了EGF刺激的S4细胞生长。用α干扰素预处理细胞不影响EGF与其受体的结合。然而,细胞暴露于γ干扰素24小时可显著增加S4细胞上EGF受体的数量。干扰素处理不影响EGF受体的内化。γ干扰素暴露4天后结合仍保持升高。对受体结合数据进行Scatchard分析表明,γ干扰素增加了结合位点的数量,而不改变受体对其配体的亲和力。这些结果表明,干扰素抑制EGF刺激的乳腺癌细胞系生长,并提示干扰素的抗增殖作用可能部分归因于其与生长因子启动途径的相互作用。