西达本胺对耐伊马替尼慢性髓系白血病细胞株K–562/Ima细胞增殖、凋亡的影响

Study of the Effects of Chidamide on Proliferation,and Apoptosis of K–562/Ima1 Cells

目的:研究西达本胺对耐伊马替尼慢性髓系白血病(CML)细胞株K–562(K–562/Ima)细胞增殖、凋亡的影响。方法:根据预实验结果,选定西达本胺(作用时间48 h)不同浓度(终浓度0、5、10、20、30 μmol·L^(-1))对K–562/Ima细胞进行干预,CCK–8法检测细胞活力即增殖能力。根据CCK–8实验结果,选定西达本胺(终浓度为0、1、3、5、7 μmol·L^(-1)),对K–562/Ima细胞进行干预,流式细胞术检测细胞的凋亡。结果:西达本胺作用K–562/Ima细胞48 h后,不同浓度均可显著抑制K–562/Ima细胞的增殖,且诱导K–562/Ima细胞凋亡,随着浓度增加,细胞增殖抑制率、凋亡率明显升高。结论:西达本胺对K–562/Ima细胞有显著的抑制增殖、促进凋亡作用,且均有浓度依赖性。

Objective The purpose of this study was to observe the effect of chidamide on the proliferation and apoptosis of K–562/Ima cell which is imatinib-resistant chronic myeloid leukemia cell lines.Methods According to the results of the preliminary experiment,the K–562/Ima cells were respectively treated by chidamide with different concentrations (final concentration 0,5,10,20,30 μmol·L^(-1)) for 48h.The cells proliferation inhibition rates were measured by CCK-8 method.Then,according to the results of the CCK-8 method,the K–562/Ima cells were treated by chidamide with different concentrations (final concentration0,1,3,5,7 μmol·L^(-1)) for 48h.The apoptosis rate was detected by flow cytometry.Results Different concentrations of chidamide were treated with K–562/Ima cells for 48 hours respectively.It was found that the inhibitory rate of cell proliferation was significantly increased with the increase of chidamide concentration,and the rate of cell apoptosis was apoptosis significantly increased with the increase of chidamide concentration.Conclusions Cedabide can significantly inhibit the proliferation and promote the apoptosis of K–562/Ima cells in a concentration-dependent manner.