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三氧化二砷联合伊曲康唑对KG1a细胞的协同杀伤作用

[Synergistic Killing Effects of Arsenic Trioxide Combined with Itraconazole on KG1a Cells].

作者信息

Wu Jian-Wei, Xiao Wei-Ting, Zeng Ying-Jian, Fan Jia-Xin, Ye Yong-Bin, Li Yuan-Ming, Zhen Rong, Guo Kun-Yuan

机构信息

Department of Hematology, Jinan University Affiliated Jiangmen Hospital of Traditional Chinese Medicine, Jiangmen 529000, Guangdong Province, China.

Department of Hematology, Jinan University Affiliated Jiangmen Hospital of Traditional Chinese Medicine, Jiangmen 529000, Guangdong Province, China. E-mail:

出版信息

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2017 Aug;25(4):1003-1010. doi: 10.7534/j.issn.1009-2137.2017.04.008.

Abstract

OBJECTIVE

To explore the effect of arsenic trioxide combined with itraconazole on proliferation and apoptosis of KG1a cells and its potential mechanism.

METHODS

The cell morphology was observed with Wrighe-Giemsa staining; cell survival rate was examined by CCK-8; and colony formation capacity was measured by methylcellulose colony formation test; the flow cytometry was used to analyse the cell apoptosis rate and cell cycle; the protein expressions of BCL-2,caspase-3,BAX,SMO,Gli1 and Gli2 were detected by Western-blot.

RESULTS

The arsenic trioxide and itraconazole alone both could inhibit the KG1a cell proliferation in dose-and time-dependent manner. In comparison between single and combined drug-treatment group, both the cell survival rate and the colony number of the single drug-treatment group were significantly lower(P<0.05), and the apoptosis rate was higher in the combined drug-treatment group. In the combined-treatment group, the protein expression of Caspase-3 and BAX was upregulated, while the protein expression of BCL-2,SMO,Gli1 and Gli2 was downregulated.

CONCLUSION

Arsenic trioxide combined with itraconazole can inhibit the KG1a cell proliferation and induce apoptosis, which may be related with the inhibition of Hh signaling pathway and upregulation of both Caspase-3 and BAX protein expression, and provided experimental data of arsenic trioxide combined with itraconazole for the treatment of refractory AML.

摘要

目的

探讨三氧化二砷联合伊曲康唑对KG1a细胞增殖和凋亡的影响及其潜在机制。

方法

采用瑞氏-吉姆萨染色观察细胞形态;用CCK-8检测细胞存活率;用甲基纤维素集落形成试验检测集落形成能力;用流式细胞术分析细胞凋亡率和细胞周期;用蛋白质免疫印迹法检测BCL-2、caspase-3、BAX、SMO、Gli1和Gli2的蛋白表达。

结果

三氧化二砷和伊曲康唑单独使用均能以剂量和时间依赖性方式抑制KG1a细胞增殖。单药治疗组与联合用药组比较,单药治疗组细胞存活率和集落数均显著降低(P<0.05),联合用药组凋亡率更高。联合治疗组中,Caspase-3和BAX的蛋白表达上调,而BCL-2、SMO、Gli1和Gli2的蛋白表达下调。

结论

三氧化二砷联合伊曲康唑可抑制KG1a细胞增殖并诱导凋亡,这可能与抑制Hh信号通路以及Caspase-3和BAX蛋白表达上调有关,为三氧化二砷联合伊曲康唑治疗难治性急性髓系白血病提供了实验数据。

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