紫杉醇
微管蛋白
细胞毒性T细胞
微管
体外
细胞培养
有丝分裂
微管聚合
作用机理
化学
生物
细胞毒性
癌细胞
药理学
生物化学
癌症研究
癌症
细胞生物学
遗传学
作者
B H Long,Joan M. Carboni,Arthur J. Wasserman,L. CORNELL,Anna Maria Casazza,Paul R. Jensen,Thomas Lindel,William Fenical,C.R. Fairchild
出处
期刊:PubMed
日期:1998-03-15
卷期号:58 (6): 1111-5
被引量:221
摘要
Eleutherobin is a novel natural product isolated from a marine soft coral that is extremely potent for inducing tubulin polymerization in vitro and is cytotoxic for cancer cells with an IC50 similar to that of paclitaxel. This compound is cross-resistant along with other multidrug-resistant agents against P-glycoprotein-expressing cells and is cross-resistant with paclitaxel against a cell line that has altered tubulin. In mechanistic studies, eleutherobin shares with paclitaxel the ability to induce tubulin polymerization in vitro and is most likely cytotoxic by virtue of this mechanism. Human colon carcinoma cells exposed to eleutherobin contain multiple micronuclei and microtubule bundles, and they arrest in mitosis, depending on concentration, cell line, and length of exposure. These morphological abnormalities appearing in cultured cells are indistinguishable from those induced by paclitaxel. Electron microscopy reveals that eleutherobin induces homogeneous populations of long, rigid microtubules similar to those formed by paclitaxel. Thus, eleutherobin is a new chemotype with a mechanism of action similar to that of paclitaxel and, as such, has promising potential as a new anticancer agent.
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