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微管解聚剂和稳定剂的低剂量同时联合使用。

Simultaneous combination of microtubule depolymerizing and stabilizing agents acts at low doses.

作者信息

Garcia P, Braguer D, Carles G, Briand C

机构信息

URA CNRS 1924, Faculté de Pharmacie, Marseille, France.

出版信息

Anticancer Drugs. 1995 Aug;6(4):533-44. doi: 10.1097/00001813-199508000-00006.

Abstract

The combined activity of a stabilizing and a depolymerizing agent was studied on microtubule formation in vitro and on cellular parameters related to the cytoskeleton. New compounds in each class of microtubular drugs, docetaxel, as stabilizing agent, and CI 980, as colchicine analog, currently in clinical trials, were tested at high and low concentrations. Simultaneous combination of docetaxel and CI 980, both in vitro and in cell lines, induced microtubule structures resulting from the association of the effects of the two drugs: short and numerous microtubules in vitro, abnormal asters or short bundles in cells depolymerized in their periphery. Moreover, combining the two drugs at low concentrations inducing neither modification of the microtubular network nor variation in cell polymerized tubulin content showed synergistic effects in mitotic cell block and, at lower concentrations, in inhibition of proliferation in the KB 3-1 cell line. Similar qualitative results were obtained with paclitaxel and colcemid, used in the place of docetaxel and CI 980, respectively. At low doses, the taxoid/colchine analog combination seems to induce some degree of mitotic inhibition, resulting from a subtle effect on the inhibition of microtubule dynamics.

摘要

研究了一种稳定剂和一种解聚剂对体外微管形成以及与细胞骨架相关的细胞参数的联合作用。在每类微管药物中,分别以处于临床试验阶段的新型化合物多西他赛作为稳定剂,以秋水仙碱类似物CI 980作为解聚剂,进行了高浓度和低浓度测试。多西他赛和CI 980在体外和细胞系中的同时联合使用,诱导出了由两种药物作用共同产生的微管结构:体外形成短而密集的微管,细胞中出现异常星状体或外周解聚的短束状结构。此外,在低浓度下联合使用这两种药物,既不改变微管网络,也不改变细胞中聚合微管蛋白的含量,但在有丝分裂细胞阻滞方面显示出协同作用,在较低浓度下,对KB 3-1细胞系的增殖有抑制作用。分别用紫杉醇和秋水仙酰胺替代多西他赛和CI 980,得到了相似的定性结果。在低剂量下,紫杉烷/秋水仙碱类似物组合似乎会诱导一定程度的有丝分裂抑制,这是对微管动力学抑制的微妙作用所致。

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