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人γ干扰素与不同敏感性的人表皮肿瘤细胞的结合

Binding of human gamma-interferon to human epidermal tumor cells with different susceptibilities.

作者信息

Nagao S, Sato K, Osada Y

出版信息

Cancer Res. 1986 Jul;46(7):3279-82.

PMID:3085920
Abstract

The in vitro antiproliferative effect of highly purified recombinant human gamma-interferon was studied with special reference to specific binding to tumor cells of interferon (IFN) labeled with 125I. Recombinant human gamma-interferon markedly suppressed the growth of 6 of 10 human epidermal tumor cell lines tested; the concentration required to inhibit the growth of susceptible cell lines by 50% ranged from 8 to 36 units/ml (13.6 to 61.2 pM), whereas those for the other cell lines were higher than 10,000 units/ml. These anticellular effects were compatible with the suppressive effects of IFN on cellular DNA synthesis. Labeled IFN bound specifically to the susceptible cells, which showed, from the Scatchard analysis, 870 to 7700 binding sites/cell with apparent Kd of 1.70 to 5.84 X 10(-11) M. There was little binding of the labeled IFN to the resistant cells and nonspecific binding occurring in the presence of a 1000-fold excess of unlabeled IFN accounted for 40 to 90% of the total binding. These results suggest that specific binding sites for recombinant human gamma-interferon exist on the resistant cell lines.

摘要

以125I标记的干扰素(IFN)与肿瘤细胞的特异性结合为特别参照,研究了高度纯化的重组人γ干扰素的体外抗增殖作用。重组人γ干扰素显著抑制了所检测的10种人表皮肿瘤细胞系中6种细胞系的生长;抑制敏感细胞系生长50%所需的浓度范围为8至36单位/毫升(13.6至61.2皮摩尔),而其他细胞系所需的浓度高于10,000单位/毫升。这些抗细胞作用与IFN对细胞DNA合成的抑制作用相符。标记的IFN特异性结合到敏感细胞上,从Scatchard分析来看,敏感细胞显示出每个细胞有870至7700个结合位点,表观解离常数为1.70至5.84×10⁻¹¹ M。标记的IFN与耐药细胞几乎没有结合,在存在1000倍过量未标记IFN的情况下发生的非特异性结合占总结合的40%至90%。这些结果表明耐药细胞系上存在重组人γ干扰素的特异性结合位点。

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