首页> 美国卫生研究院文献>British Journal of Cancer >Ability of sera from mice treated with Ge-132 an organic germanium compound to inhibit experimental murine ascites tumours.
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Ability of sera from mice treated with Ge-132 an organic germanium compound to inhibit experimental murine ascites tumours.

机译:用有机锗化合物Ge-132处理的小鼠的血清抑制实验鼠腹水肿瘤的能力。

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摘要

Sera from C57Bl/6 mice treated orally with Ge-132 exhibited antitumour activity against Ehrlich (allogeneic) and RL male 1 (syngeneic) ascites tumours in BALB/c mice. Sera obtained from mice 24 h after Ge-132 administration displayed the greatest antitumour effect and this was dose dependent. Sera prepared from mice 12, 36, or 48 h after Ge-132 treatment had no protective effect. Circulating interferon (IFN) was induced at 24 h after administration of Ge-132 but was not detected in the sera at 12, 36, or 48 h after administration. The antiviral activity of sera from Ge-132-treated mice was inactivated by treatments with trypsin, low pH, and anti-IFN gamma antiserum. The inactivated preparations of serum IFN induced by Ge-132 did not exhibit antitumour activity when administered to tumour-bearing mice. These results suggest that antitumour activity in the sera of Ge-132-treated mice may be expressed through activities of Ge-132-induced lymphokine(s), such as IFN gamma.
机译:用Ge-132口服治疗的C57Bl / 6小鼠的血清对BALB / c小鼠的Ehrlich(同基因)和RL雄性1(同基因)腹水肿瘤表现出抗肿瘤活性。 Ge-132给药后24小时从小鼠获得的血清显示出最大的抗肿瘤作用,这是剂量依赖性的。在Ge-132处理后的12、36或48 h从小鼠制备的血清没有保护作用。施用Ge-132后24小时诱导了循环干扰素(IFN),但在施用后12、36或48 h在血清中未检测到循环干扰素。用胰蛋白酶,低pH和抗IFNγ抗血清处理可灭活Ge-132处理的小鼠血清的抗病毒活性。当对荷瘤小鼠给药时,由Ge-132诱导的血清IFN灭活制剂没有抗肿瘤活性。这些结果表明,通过Ge-132诱导的淋巴因子,例如IFNγ的活性,可以表达Ge-132治疗的小鼠的血清中的抗肿瘤活性。

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