李佩玲, 刘梅梅, 倪江. 泰素诱导卵巢癌细胞凋亡及其作用途径的体外初步观察[J]. 中国肿瘤临床, 2004, 31(7): 372-375.
引用本文: 李佩玲, 刘梅梅, 倪江. 泰素诱导卵巢癌细胞凋亡及其作用途径的体外初步观察[J]. 中国肿瘤临床, 2004, 31(7): 372-375.
Li Pei-ling, Liu Mei-mei, Ni Jiang. Taxol Mediated Apoptosis May Involve Pathways Other than Microtubule Stabilization[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2004, 31(7): 372-375.
Citation: Li Pei-ling, Liu Mei-mei, Ni Jiang. Taxol Mediated Apoptosis May Involve Pathways Other than Microtubule Stabilization[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2004, 31(7): 372-375.

泰素诱导卵巢癌细胞凋亡及其作用途径的体外初步观察

Taxol Mediated Apoptosis May Involve Pathways Other than Microtubule Stabilization

  • 摘要: 目的:体外实验评价泰素在不同卵巢癌细胞中对细胞骨架的作用,以证实泰素不仅是通过微管稳定而发挥作用.方法:将人类卵巢癌细胞系OVCA-420和最近分离的6个卵巢上皮实体肿瘤细胞成分暴露于不同浓度的泰素处理后,通过免疫荧光染色细胞骨架中的微管蛋白和肌动蛋白来评估各种细胞骨架之间的区别.结果:对照组OVCA-420细胞系在核周有过多的核仁纤维组织,而该细胞核在泰素处理后虽有多核可见,但上述现象并没有变化.一部分经离体培养的癌细胞在经泰素治疗后已经分散,可见点状的肌动蛋白成簇聚集于微核部位;而另一部分离体培养的癌细胞经泰素处理后聚集的微管围绕在细胞核周围,并没有明显的多核现象.结论:泰素在不同离体培养的卵巢癌细胞中的作用是不同的,但在同一类型的卵巢癌细胞中作用是相似的,即微管稳定;泰素的作用与浓度具有一定的相关性;肌动蛋白对泰素的反应与多核现象出现背离情况;泰素可能通过不同于微管稳定路径而是其他作用机制发挥作用.

     

    Abstract: Objective: To evaluate the effects of Taxol on the cytoskeleton of different ovarian cells and to prove that there may be a different mechanism of action for Taxol other than through microtubulin stabilization. Methods: A human ovarian cancer cell line (0VCA-420) and the solid component from six recently isolated epithelial ovarian tumors were exposed to Taxol(20uM and 50nM).The cells were evaluated for differences in the cytoskeleton by immunostaining for tubulin and actin.Results: Multimininucleation, which is consistent with apoptotic nuclei, was identified using Hoerscht D N A staining. All the cells exhibited an organized cytoskeleton when stained for actin. The control OVCA-420 cells had an extensive fibrillar tubulin organization around the nucleus which did not change in appearance after treatment which Taxol, despite the multimininucleation which occurred. In contrast, the control cells (for example HS-1) had diffuse, punctate tubulin which then accumulated in bundles at the sites of frequent mininuclei after treatment with Taxol. The other cells (for example HS-2), after treatment with Taxol, accumulated tubulin around the periphery of the nucleus. However, there was no evidence of multinucleation. Conclusions: The effect of Taxol on tubulin varies between ovarian cancer cell populations, but is homogenous within a cell population. There also appears to be a dissociation between tubulin response to Taxol and multimininucleation. Therefore, there may be a different mechanism of action for Taxol other than through microtubulin stabilization.

     

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