首页|miR-217靶向PI3K/Akt通路增强阿霉素对急性髓系白血病的敏感性

miR-217靶向PI3K/Akt通路增强阿霉素对急性髓系白血病的敏感性

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目的:探讨miR-217对急性髓系白血病细胞增殖及阿霉素敏感性的影响.方法:构建mimic NC和miR-217 mimic载体转染至HL-60细胞中,qPCR检测转染效率.不同浓度的阿霉素处理细胞24和48 h,CCK-8法检测阿霉素化学敏感性并筛选阿霉素的最佳处理浓度和时间.将细胞分为对照、mimic NC、miR-217 mimic、阿霉素和miR-217 mimic+阿霉素共5组,流式细胞术检测细胞凋亡,qPCR检测miR-217、PI3K和Akt3的表达,Western blot检测PI3K/Akt通路蛋白PI3K、Akt3和凋亡蛋白Bcl-2、Bax的表达,双荧光素酶验证miR-217和Akt3的关系.结果:miR-217 mimic能够增强HL-60细胞对阿霉素的敏感性,阿霉素的最佳处理浓度和时间为160 ng/ml、48 h.与对照组相比,miR-217 mimic组和阿霉素组细胞凋亡率、miR-217和Bax蛋白水平显著升高(P<0.01),而Bcl-2蛋白和PI3K、Akt3 mRNA和蛋白水平显著降低(P<0.01);与阿霉素组相比,miR-217 mimic+阿霉素组细胞凋亡率、miR-217和Bax蛋白水平显著升高(P<0.01),Bcl-2蛋白和PI3K、Akt3 mRNA和蛋白水平显著降低(P<0.01).双荧光素酶实验表明miR-217 与Akt3之间存在靶向调控关系.结论:miR-217靶向Akt3调控PI3K/Akt通路,抑制细胞增殖,促进细胞凋亡并增强阿霉素对急性髓系白血病细胞的敏感性.
MiR-217 Targeting PI3K/Akt Pathway Enhances Sensitivity of Adriamycin to Acute Myeloid Leukemia
Objective:To investigate the effects of miR-217 on proliferation and adriamycin sensitivity of acute myeloid leukemia(AML)cells.Methods:The mimic NC and miR-217 mimic vectors were constructed and transfected into HL-60 cells,and transfection efficiency was detected by qPCR.The cells were treated with different concentrations of adriamycin for 24 h and 48 h.CCK-8 assay was used to detect the chemical sensitivity of adriamycin and screen the optimal concentration and time of adriamycin treatment.Cells were divided into control group,mimic NC group,miR-217 mimic group,adriamycin group and miR-217 mimic+adriamycin group.Apoptosis was detected by flow cytometry,and the expressions of miR-217,PI3K and Akt3 were detected by qPCR.Western blot was used to detect the expression of PI3K/Akt pathway proteins PI3K,Akt3 and apoptosis proteins Bcl-2,Bax,and double luciferase was used to verify the relationship between miR-217 and Akt3.Results:MiR-217 mimic could enhance the sensitivity of HL-60 cells to adriamycin.The optimal concentration and treatment time of adriamycin were 160 ng/ml and 48 h,respectively.Compared with control group,apoptosis rate,miR-217 and Bax protein levels were significantly increased in miR-217 mimic and adriamycin groups(P<0.01),while Bcl-2 protein,PI3K,Akt3 mRNA and protein levels were significantly decreased(P<0.01).Compared with adriamycin group,apoptosis rate,miR-217 and Bax protein levels were significantly increased in miR-217 mimic+adriamycin group(P<0.01),while Bcl-2 protein,PI3K,Akt3 mRNA and protein levels were significantly decreased(P<0.0 1).Dual luciferase assay showed that there was a targeted regulatory relationship between miR-217 and Akt3.Conclusion:MiR-217 regulates the PI3K/Akt pathway targeting Akt3,inhibits cell proliferation,promotes cell apoptosis and enhances the sensitivity of adriamycin to AML cells.

miR-217acute myeloid leukemiaadriamycinPI3K/Akt pathway

干定云、吴军、周曼、陈婉、姜雯

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武汉市第三医院血液内科,湖北武汉 430070

miR-217 急性髓系白血病 阿霉素 PI3K/Akt通路

湖北省卫生健康委科研项目武汉市卫生健康委医学科研项目

WJ2021M012WX20B31

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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