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肿瘤DNA在同源培养系统中诱导干扰素生成

Interferon induction by a tumoral DNA in an homologous culture system.

作者信息

de Kohan S S, Teyssie A R, de Pirosky R R, Loria D, de Holstein B A

出版信息

Biomedicine. 1975 Dec 20;23(10):419-22.

PMID:177113
Abstract

The interferon induction by Rous sarcoma DNA in an homologous culture system and a further insight of its kinetics and antimetabolites action were the principal aim of the present study. There was a direct relation between the dose of the inducer and the protection against the cytoplathogenic effect of the challenging virus (VSV) reaching the highest activity (68-75% CPE inhibition) with 100 mug RS-DNA. The kinetics of the induction revealed a peak inhibition by 18 hours after the inducer. Treatment with Actinomycin D evidenced that both interferon production and activity are modified. Its early addition resulted in a poor protection; but an accentuated interferon release was observed when antimetabolite was added 18 hours after the inducer. Similar results were obtained when its effect was studied on the activity of exogenous interferon. Interferon induction by Rous sarcoma DNA in an homologous system, allows the detection of a difference between tumoral and normal DNA at a biological level.

摘要

本研究的主要目的是在同源培养系统中研究劳氏肉瘤DNA诱导干扰素的情况,并进一步深入了解其动力学及抗代谢物的作用。诱导剂剂量与针对攻击病毒(水泡性口炎病毒,VSV)细胞病变效应的保护作用之间存在直接关系,100微克劳氏肉瘤DNA时达到最高活性(68 - 75%抑制细胞病变效应)。诱导动力学显示,诱导剂作用18小时后抑制作用达到峰值。放线菌素D处理表明,干扰素的产生和活性均发生了改变。早期添加放线菌素D导致保护作用不佳;但在诱导剂作用18小时后添加抗代谢物时,观察到干扰素释放增强。研究其对外源干扰素活性的影响时也得到了类似结果。在同源系统中劳氏肉瘤DNA诱导干扰素,能够在生物学水平上检测肿瘤DNA与正常DNA之间的差异。

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