Sheridan V R, Speicher L A, Tew K D
Department of Pharmacology, Fox Chase Cancer Center, Philadelphia, PA 19111.
Eur J Cell Biol. 1991 Apr;54(2):268-76.
The chemotherapeutic drug, estramustine, has been shown to cause the disassembly of microtubules via binding to microtubule-associated proteins. In this report, estramustine is shown to be a potent inhibitor of mitotic progression in the human prostatic carcinoma cell line, DU 145. Examination of individual living cells via video-enhanced differential interference contrast (DIC) optics shows that the drug delays the onset of anaphase, reduces anaphase spindle-pole elongation (anaphase B), and delays cytokinesis. In addition, immunofluorescent studies demonstrate that estramustine causes a rapid disorganization of the mitotic apparatus at significantly lower concentrations than those reported previously. Electron microscopic studies show that microtubule bundles are present in drug-treated mitotic cells in association with kinetochores and centrioles.
化疗药物雌莫司汀已被证明可通过与微管相关蛋白结合导致微管解聚。在本报告中,雌莫司汀被证明是人类前列腺癌细胞系DU 145有丝分裂进程的有效抑制剂。通过视频增强微分干涉相差(DIC)光学显微镜对单个活细胞进行观察显示,该药物会延迟后期开始,减少后期纺锤体极伸长(后期B),并延迟胞质分裂。此外,免疫荧光研究表明,与之前报道的浓度相比,雌莫司汀在显著更低的浓度下就能使有丝分裂器迅速解体。电子显微镜研究显示,在经药物处理的有丝分裂细胞中,微管束与动粒和中心粒相关联。