汪进, 何放亭, 曾志雄, 方宏勋, 肖培根, 韩锐, 杨梦甦. 紫杉醇诱导人乳腺癌MCF-7细胞周期阻断及凋亡的基因表达谱分析J. 药学学报, 2005, 40(12): 1099-1104.
引用本文: 汪进, 何放亭, 曾志雄, 方宏勋, 肖培根, 韩锐, 杨梦甦. 紫杉醇诱导人乳腺癌MCF-7细胞周期阻断及凋亡的基因表达谱分析J. 药学学报, 2005, 40(12): 1099-1104.
WANG Jin, HE Fang-ting, TZANG Chi-hung, FONG Wang-fan, XIAO Pei-gen, HAN Rui, YANG Meng-su. Differential gene expression profiles in paclitaxel-induced cell cycle arrest and apoptosis in human breast cancer MCF-7 cellsJ. Acta Pharmaceutica Sinica, 2005, 40(12): 1099-1104.
Citation: WANG Jin, HE Fang-ting, TZANG Chi-hung, FONG Wang-fan, XIAO Pei-gen, HAN Rui, YANG Meng-su. Differential gene expression profiles in paclitaxel-induced cell cycle arrest and apoptosis in human breast cancer MCF-7 cellsJ. Acta Pharmaceutica Sinica, 2005, 40(12): 1099-1104.

紫杉醇诱导人乳腺癌MCF-7细胞周期阻断及凋亡的基因表达谱分析

Differential gene expression profiles in paclitaxel-induced cell cycle arrest and apoptosis in human breast cancer MCF-7 cells

  • 摘要: 目的研究紫杉醇诱导人MCF-7细胞周期阻断及凋亡的分子机制。方法用流式细胞仪分析紫杉醇对MCF-7细胞周期变化的影响,用自制的含9 984个已知基因和EST的高密度基因芯片检测MCF-7细胞在不同浓度紫杉醇作用下的基因表达变化。结果MCF-7细胞在100 nmol·L-1紫杉醇作用24 h,流式细胞仪结果显示77.8%细胞阻断在G2/M期和1.3%细胞发生凋亡;基因表达谱分析发现:在12.5 nmol·L-1 (IC50)及100 nmol·L-1紫杉醇作用下,分别有27及77个基因差异表达。结论紫杉醇可诱导MCF-7细胞周期阻断在G2/M期并引起部分细胞凋亡,该作用与药物浓度有关。基因表达谱分析显示部分差异表达基因参与细胞微管及骨架结构、细胞周期调控、以及DNA损伤修复和凋亡过程。

     

    Abstract: AimTo elucidate the molecular mechanism of cell cycle arrest and apoptosis of MCF-7 cells induced by paclitaxel. MethodsFlow cytometry was used to determine the cell cycle changes of MCF-7 cells upon paclitaxel treatment. Gene expression profiles of MCF-7 cells induced by paclitaxel were obtained by using cDNA microarrays containing 9 984 genes and expressed sequence tags (ESTs). Results Cell cycle analysis showed that 77.8% of cells arrested at G2/M phase and 1.3% of cells underwent apoptosis upon 100 nmol·L-1 paclitaxel treatment for 24 hours; cDNA microarray results revealed that 27 and 77 genes were differentially expressed upon 12.5 nmol·L-1 (IC550) and 100 nmol·L-1 paclitaxel treatment, respectively. ConclusionPaclitaxel stabilized microtubules and caused G2/M cell cycle arrest and apoptotic cell death in a concentration-dependent manner, which is associated with the regulation of selected genes related to microtubule assembly and cytoskeleton, cell cycle regulation, and DNA repair and apoptosis.

     

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