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肿瘤启动子和蛋白酶抑制剂在体外对辐射转化进行修饰的条件。

The conditions for the modification of radiation transformation in vitro by a tumor promoter and protease inhibitors.

作者信息

Kennedy A R

出版信息

Carcinogenesis. 1985 Oct;6(10):1441-5. doi: 10.1093/carcin/6.10.1441.

Abstract

These experiments were designed to define the conditions necessary for the modification of radiation-induced transformation in C3H/10T1/2 cells by TPA and protease inhibitors. The results show that: (i) the lowest effective dose of various protease inhibitors to suppress transformation in vitro varies over several orders of magnitude; on a molar basis, the inhibitors of chymotrypsin appear to be the most effective protease inhibitors at suppression of radiation-induced transformation in vitro, (ii) the protease inhibitors antipain and the Bowman-Birk (soybean) protease inhibitor have no effect on radiation transformation when present only during irradiation, (iii) the protease inhibitor antipain can suppress radiation transformation in vitro when applied to proliferating "initiated' cells as late as 10 days and 13 cell divisions post-irradiation, and (iv) TPA treatment following a 10-day protease inhibitor (anti-pain) exposure of X-irradiated "initiated' cells does not lead to promotion in vitro. These results suggest that protease inhibitor treatment of the initiated cells has irreversibly reverted cells to their original or "uninitiated' condition which existed before irradiation.

摘要

这些实验旨在确定佛波酯(TPA)和蛋白酶抑制剂对C3H/10T1/2细胞中辐射诱导转化进行修饰所需的条件。结果表明:(i)各种蛋白酶抑制剂在体外抑制转化的最低有效剂量相差几个数量级;以摩尔计,胰凝乳蛋白酶抑制剂似乎是体外抑制辐射诱导转化最有效的蛋白酶抑制剂,(ii)蛋白酶抑制剂抗痛素和鲍曼-伯克(大豆)蛋白酶抑制剂仅在照射期间存在时对辐射转化无影响,(iii)蛋白酶抑制剂抗痛素在照射后10天和13个细胞分裂时应用于增殖的“启动”细胞时,可在体外抑制辐射转化,以及(iv)经X射线照射的“启动”细胞在蛋白酶抑制剂(抗痛素)暴露10天后进行TPA处理不会导致体外促进作用。这些结果表明,对启动细胞进行蛋白酶抑制剂处理已使细胞不可逆地恢复到照射前存在的原始或“未启动”状态。

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