Isbrucker Richard A, Cummins Jennifer, Pomponi Shirley A, Longley Ross E, Wright Amy E
Harbor Branch Oceanographic Institution, Inc., Division of Biomedical Marine Research, 5600 US 1 North, Fort Pierce, FL 34946, USA.
Biochem Pharmacol. 2003 Jul 1;66(1):75-82. doi: 10.1016/s0006-2952(03)00192-8.
Dictyostatin-1 had previously been isolated from a marine sponge of the genus Spongia sp. and described as a cytotoxic agent to murine and human cancer cells, but its mechanism of activity was unknown. In a routine screening assay used to detect cytotoxic compounds of marine origin, dictyostatin-1 was identified as a highly active component in an extract from a Lithistida sponge and exploration into its pharmacology was pursued. Initial studies demonstrated that dictyostatin-1 arrested cells in the G(2)/M phase of the cell cycle. Staining of these cells with antitubulin revealed cells having multiple aster formations and microtubule matrix bundling patterns similar to that seen in cells exposed to paclitaxel. Dictyostatin-1 was able to induce the polymerization of purified bovine brain tubulin in vitro and the polymerized tubulin remained stable at cold temperatures. Dictyostatin-1 also proved to be highly potent in two paclitaxel-resistant human cancer cell lines expressing active P-glycoprotein. Together, these results indicate that dictyostatin-1 is a potent inducer of tubulin polymerization and retains activity in cells expressing the P-glycoprotein efflux pump.
双鞭甲藻素 -1 先前是从一种海绵属(Spongia sp.)的海洋海绵中分离出来的,并被描述为对鼠类和人类癌细胞具有细胞毒性的药物,但其活性机制尚不清楚。在用于检测海洋来源细胞毒性化合物的常规筛选试验中,双鞭甲藻素 -1 被鉴定为一种来自石海绵纲海绵提取物中的高活性成分,并对其药理学进行了探索。初步研究表明,双鞭甲藻素 -1 使细胞停滞在细胞周期的 G(2)/M 期。用抗微管蛋白对这些细胞进行染色,发现细胞具有多个星体形成以及微管基质束状模式,这与在接触紫杉醇的细胞中所见的相似。双鞭甲藻素 -1 能够在体外诱导纯化的牛脑微管蛋白聚合,并且聚合后的微管蛋白在低温下保持稳定。双鞭甲藻素 -1 在两种表达活性 P - 糖蛋白的紫杉醇耐药人类癌细胞系中也被证明具有高效性。总之,这些结果表明双鞭甲藻素 -1 是微管蛋白聚合的强效诱导剂,并且在表达 P - 糖蛋白外排泵的细胞中保持活性。