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一种黄原酸盐化合物在实验性小鼠皮肤肿瘤发生中的肿瘤预防作用。

Tumor prevention by a xanthate compound in experimental mouse-skin tumorigenesis.

作者信息

Fürstenberger G, Amtmann E, Marks F, Sauer G

机构信息

Institute for Biochemistry, German Cancer Research Center, Heidelberg, FRG.

出版信息

Int J Cancer. 1989 Mar 15;43(3):508-12. doi: 10.1002/ijc.2910430328.

Abstract

The antiviral and antitumoral compound tricyclodecan-9-yl-xanthogenate (D609), which is an inhibitor of protein kinase C activation, has been used for tumor prevention in vivo. When applied chronically together with 12-O-tetradecanoylphorbol-13-acetate (TPA) in the classic initiation-promotion mouse-skin model, D609 prevented tumor induction in a dose-dependent manner. At the concentration that inhibited tumor formation by 97%, no toxic effects were detected and the TPA-induced hyperplasia remained unaffected. As D609 failed to prevent the activity of a chronically applied carcinogen, it is concluded that the observed tumor prevention achieved with D609 is tumor-promotion-specific and is not due to killing of tumor cells.

摘要

抗病毒和抗肿瘤化合物三环癸烷-9-基-黄原酸酯(D609)是蛋白激酶C激活的抑制剂,已用于体内肿瘤预防。在经典的启动-促进小鼠皮肤模型中,当与12-O-十四烷酰佛波醇-13-乙酸酯(TPA)长期联合应用时,D609以剂量依赖的方式预防肿瘤诱导。在抑制肿瘤形成达97%的浓度下,未检测到毒性作用,且TPA诱导的增生未受影响。由于D609未能阻止长期应用致癌物的活性,得出的结论是,观察到的D609实现的肿瘤预防是肿瘤促进特异性的,并非由于杀死肿瘤细胞。

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