拓扑异构酶ii抑制剂NC-190降低小鼠肿瘤细胞胸苷激酶mRNA水平。

Kazunori Samata, Takehiro Yamagishi, Tomotake Ikeda, Aiko Kuraishi, Shiro Nakaike, Makoto Tanaka, Keiko Kashiwagi, Kazuei Igarashi
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引用次数: 0

摘要

新型抗肿瘤化合物NC-190与NC-190共同培养48 h后,对FM3A细胞的生长有较强的抑制作用,IC50值为0.019 μ g/ml (0.042 μ m)。NC-190对DNA合成有较强的抑制作用,在0.1 μ g/ml NC-190浓度下,抑制率达90%。在相同的条件下,RNA和蛋白质的合成也受到抑制,但程度较轻。然后,我们测量了添加或不添加NC-190的FM3A细胞的DNA聚合酶α、RNA聚合酶、胸苷激酶、胸苷酸合成酶和Leu-tRNA合成酶的细胞酶活性。在这5种酶中,NC-190对胸苷激酶活性的抑制作用最强,达到77%。虽然NC-190在无细胞系统中不直接抑制胸苷激酶的活性,但NC-190处理的细胞中胸苷激酶mRNA的表达被抑制了75%。这些结果表明NC-190可以抑制胸苷激酶基因的表达,抑制胸苷激酶有助于NC-190抑制细胞生长,同时抑制拓扑异构酶II。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The topoisomerase II-inhibitor NC-190 reduces the level of thymidine kinase mRNA in murine tumor cells.

The novel antitumor compound NC-190 strongly inhibited the growth of FM3A cells with an IC50 of 0.019 microg/ml (0.042 microM) when cultured with NC-190 for 48 h. NC-190 potently suppressed DNA synthesis, with 90% inhibition observed at 0.1 microg/ml of NC-190. RNA and protein syntheses were also suppressed under the same conditions, but to a lesser extent. We then measured the cellular enzymatic activities of DNA polymerase alpha, RNA polymerase, thymidine kinase, thymidylate synthase and Leu-tRNA synthetase of FM3A cells cultured with or without NC-190. Of these 5 enzymes, the activity of thymidine kinase was most strongly suppressed by NC-190, by 77%. Although NC-190 did not directly inhibit the activitiy of thymidine kinase in a cell-free system, expression of mRNA of thymidine kinase was suppressed by 75% in NC-190-treated cells. These results indicate that NC-190 can suppress the expression of the gene for thymidine kinase and the inhibition of thymidine kinase contributes to the inhibition of cell growth by NC-190 together with the inhibition of topoisomerase II.

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