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拓扑替康诱导卵巢癌COC1/ DDP 细胞凋亡的分子机制初步探讨

Molecular Mechanism of Apoptosis in Cisplatin-resistant Human Ovarian Cancer Cell Line Promoted by Topotecan

  • 摘要: 目的 探讨拓扑替康(TPT)对人卵巢癌顺铂耐药细胞株COC1/DDP的杀伤和诱导凋亡活性及其作用机制。方法 MTT比色法与软琼脂克隆形成测定TPT对人卵巢癌顺铂耐药细胞株COC1/DDP的杀伤效应;TUNEL法和流式细胞仪研究TPT对靶细胞的凋亡诱导作用;Western blot检测TPT对COC1/DDP细胞内bcl-2、bax和caspase-3基因表达的影响以及caspase-3活性的改变。结果 TPT对COC1/DDP细胞有明显细胞毒性作用,不仅有剂量依赖性,也存在明显的时间依赖性;COC1/DDP细胞在TPT作用后出现特征性凋亡形态特征,且凋亡率由8.54%上升为23.16%(P<0.05)。TPT不影响COC1/DDP细胞内bcl-2蛋白表达,却明显增加19ax蛋白和caspase-3蛋白表达,并提高caspase-3活性。结论 TPT对人卵巢癌顺铂耐药细胞株COC1/DDP有明显的杀伤和促凋亡作用,其机制可能依赖于细胞内bax蛋白表达增高和caspase-3的活化。

     

    Abstract: Objective  To investigate the cytotoxicity and proapoptotic activity of topotecan ( TPT) on cisplatin - resistant human ovarian cancer cell lines COC1/ DDP and its mocular mechanisms. Methods  The cytotoxicity of TPT on COC1/ DDP was monitered using MTT assay and sof t agaragar assay. TUNEL and flow cytometry were employed to observe the apoptosis of COC1/ DDP induced by topotecan. Western blot were used to determine the expression of bcl-2, bax and caspase-3, in addition to the activity of caspase-3. Results  TPT had strong cytotoxicity on COC1/ DDP cell in vit ro, and the cytotoxicity was dose-and time-dependent . TPT treated cells demonst rated apoptosis property while the apoptotic rate was increased from 8. 54 % to 23. 16 %( P < 0. 05) . Although the expression of bcl-2 was not affected, the expression of bax and caspase-3 were upregulated and the caspase-3 activity was promoted in the course of COC1/ DDP apoptosis when t reated with topotecan. Conclusion  The cytotoxicity and proapoptosis activity of TPT, which is significantly observed in cisplatin-resistant human ovarian cancer, may be related to the increased bax expression and the promoted caspase-3 activity.

     

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