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苏拉明与喜树碱的体外序列依赖性协同作用。

In vitro sequence-dependent synergistic effect of suramin and camptothecin.

作者信息

Lopez R, Peters G J, Smitskamp-Wilms E, Virizuela J A, van Ark-Otte J, Pinedo H M, Giaccone G

机构信息

Hospital Txagorritxu, Vitoria, Spain.

出版信息

Eur J Cancer. 1994;30A(11):1670-4. doi: 10.1016/0959-8049(94)00321-u.

Abstract

Suramin, a hexasulphonated naphthylurea with activity in prostatic cancer, possesses a wide variety of antitumour mechanisms of action, one of which is the inhibition of topoisomerase II. In this in vitro study, suramin was combined with the topoisomerase I inhibitor, camptothecin. Several suramin concentrations (0.2-3000 microM) were combined with camptothecin (0.4 pM-20 microM) in MCF-7 and PC3 human cancer cell line cultures. In addition, we studied the topoisomerase II and I gene expression by northern blot analysis, and the cell cycle distribution by flow cytometry, after exposure to suramin. While there was only an additive effect when suramin and camptothecin were added simultaneously, a remarkable synergism was obtained when camptothecin was added after a 3-day exposure to suramin. Topoisomerase II and I gene expression and the number of cells in S phase were significantly reduced after exposure to suramin. In conclusion, interaction of suramin with camptothecin is schedule-dependent and can be synergistic. These findings might help in identifying optimal combinations of suramin or other topoisomerase II inhibitors, with topoisomerase I inhibitors.

摘要

苏拉明是一种在前列腺癌中具有活性的六磺化萘脲,具有多种抗肿瘤作用机制,其中之一是抑制拓扑异构酶II。在这项体外研究中,苏拉明与拓扑异构酶I抑制剂喜树碱联合使用。在MCF-7和PC3人癌细胞系培养物中,将几种苏拉明浓度(0.2 - 3000微摩尔)与喜树碱(0.4皮摩尔 - 20微摩尔)联合使用。此外,我们在暴露于苏拉明后,通过Northern印迹分析研究了拓扑异构酶II和I的基因表达,并通过流式细胞术研究了细胞周期分布。当苏拉明和喜树碱同时添加时仅产生相加作用,而在暴露于苏拉明3天后添加喜树碱则获得了显著的协同作用。暴露于苏拉明后,拓扑异构酶II和I的基因表达以及S期细胞数量显著减少。总之,苏拉明与喜树碱的相互作用是时间依赖性的,并且可以是协同的。这些发现可能有助于确定苏拉明或其他拓扑异构酶II抑制剂与拓扑异构酶I抑制剂的最佳组合。

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