首页|二甲双胍与三氧化二砷对KG1a细胞增殖的抑制作用

二甲双胍与三氧化二砷对KG1a细胞增殖的抑制作用

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目的:探讨二甲双胍协同三氧化二砷对急性髓系白血病KG1a细胞增殖的影响及其可能的机制.方法:采用CCK-8法检测二甲双胍、三氧化二砷以及联合应用对KG1a细胞的杀伤作用;Annexin V-FITC/PI双染法流式细胞术检测应用二甲双胍协同三氧化二砷对KG1a细胞凋亡的影响;Western blot检测胞内凋亡、自噬相关蛋白的表达.结果:二甲双胍与三氧化二砷联合及单独应用均可抑制KG1a细胞增殖,诱导KG1a细胞凋亡,联合用药组增殖抑制率及凋亡率高于单独用药组(P<0.05).联合用药诱导KG1a细胞中Caspase 8和P62蛋白表达上调且高于单药组(P<0.05).结论:二甲双胍能协同三氧化二砷杀伤KG1a细胞,其作用机制可能与诱导凋亡和增强自噬有关.
Inhibitory Effect of Metformin and Arsenic Trioxide on KG1a Cell Proliferation
Objective:To investigate the effect of metformin and arsenic trioxide on KG1a cells proliferation of acute myeloid leukemia and its possible mechanism.Methods:CCK-8 method was used to detect the killing effect of metformin,arsenic trioxide and combined application on KG1a cells.Annexin V-FITC/P1 Dual Stain Flow Cytometry was used to detect the effect of combined application on apoptosis of KG1 a cells.Western blot was used to detect the expression of intracellular apoptosis-,autophagy-related protein.Results:Metformin and arsenic trioxide alone or in combination could inhibit the proliferation of KG1 a cells and induce apoptosis of KG1 a cells,and the proliferation inhibition rate and apoptosis rate in the combined drug group were higher than those in the drug group alone(P<0.05).The combination of drugs induced upregulation of Caspase 8 protein and P62 protein expression and was higher than that in the drug group alone(P<0.05).Conclusion:Metformin can synergize with arsenic trioxide to kill KG1a cells,and its mechanism of action may be related to inducing apoptosis and enhancing autophagy.

arsenic trioxidemetforminacute myeloid leukemiaCaspase 8P62

黄李文惠、刘萌、桂淑敏、冯明明、刘慧、司晓慧、牛新清

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新乡医学院医学技术学院

河南省免疫与靶向药物重点实验室

河南省分子诊断与医学检验技术协同创新中心,河南新乡453003

三氧化二砷 二甲双胍 急性髓系白血病 Caspase 8 P62

国家自然科学基金河南省自然科学基金高等学校学科创新引智计划(111计划)

81800139182300410300D20036

2024

中国实验血液学杂志
中国病理生理学会

中国实验血液学杂志

CSTPCD北大核心
影响因子:0.988
ISSN:1009-2137
年,卷(期):2024.32(1)
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