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热疗联合足叶乙甙对K562 体外抑制效应及bcl-2 的表达[J]. 肿瘤防治研究, 2007, 34(04): 293-296. DOI: 10.3971/j.issn.1000-8578.1656
引用本文: 热疗联合足叶乙甙对K562 体外抑制效应及bcl-2 的表达[J]. 肿瘤防治研究, 2007, 34(04): 293-296. DOI: 10.3971/j.issn.1000-8578.1656
The Suppression Effect and bcl-2 Expression of K562 with Etoposide and Hyperthermia in Vitro[J]. Cancer Research on Prevention and Treatment, 2007, 34(04): 293-296. DOI: 10.3971/j.issn.1000-8578.1656
Citation: The Suppression Effect and bcl-2 Expression of K562 with Etoposide and Hyperthermia in Vitro[J]. Cancer Research on Prevention and Treatment, 2007, 34(04): 293-296. DOI: 10.3971/j.issn.1000-8578.1656

热疗联合足叶乙甙对K562 体外抑制效应及bcl-2 的表达

The Suppression Effect and bcl-2 Expression of K562 with Etoposide and Hyperthermia in Vitro

  • 摘要: 目的 观察热疗联合足叶乙甙增强对K562的体外增殖的抑制作用及对其凋亡、bcl-2表达的影响。方法 采用MTT法测定确定VP16的工作浓度,以该浓度进行化疗或与热疗的联合,选择温度40℃、42℃,体外作用于K562。48小时及作用前均采用台盼蓝拒染法检测肿瘤细胞的存活率;MTT法检测对肿瘤细胞增殖的抑制作用;流式细胞仪检测作用后肿瘤细胞的凋亡及bcl-2的表达。观察热疗联合足叶乙甙的抗肿瘤作用。结果 以作用48小时IC50的值作为实验的工作浓度。单纯40℃、42℃热疗60分钟在48小时对K562细胞系有抑制作用(P〈0.01),并随温度增高而增强;单纯化疗对K562细胞系也有明显抑制作用(P〈0.01);热化疗组在40℃、42℃温度下,对K562均有显著的抑制作用(P〈0.01),随着温度的增高而增强。热疗组、化疗组、热化疗组细胞凋亡率均较对照组显著升高,各组之间均有显著性差异(P〈0.01);bcl-2蛋白的表达下降,各组之间也有显著性差异(P〈0.01)。结论 热疗联合足叶乙甙能增强对K562细胞的体外抑制作用;热化疗联合应用可以提高肿瘤细胞的凋亡率,下调bcl-2的表达。

     

    Abstract: Objective  To observe the inhibitive effect, the apoptosis and bcl-2 expression of K562 cells with etoposide and hyperthermia. Methods  The working concent ration of etoposide against K562 cells was determined by MTT assay. Then hyperthermia and chemotherapy were used singly or concurrently and the cell survival rates were obtained at 48h. The inhibitive effect was evaluated by MTT assay. The apoptosis rates and bcl-2 expression of K562 were determined at 48h by flow cytomet ric. Results  The concent ration of etoposide was defined as those of IC50. The 40 ℃,42 ℃hyperthermia of 60min showed obvious inhibition to K562 cells ( P < 0. 01), etoposide chemotherapy or hyperthermia both obviously inhibited the growth of K562 cells ( P < 0. 01), etoposide chemotherapy combined with hyperthermia showed obvious effect to K562 cells. According to flow cytomet ric analyses, the treatment of hyperthermia and etoposide used alone or concurrently could obviously increase the apoptosis rates and down-regulate of bcl-2 expression of K562 cells. Conclusion  Etoposide chemotherapy combined with hyperthermia showed obvious inhibitive effect to K562 cells. The effect can increase the apoptosis rates and down-regulate of bcl-2.

     

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