Effect of DNA Methyltransferase Inhibitor SGI-1027 on Proliferation and Apoptosis of Human Hepatocellular Carcinoma Cells
10.12007/j.issn.0258-4646.2017.09.009
- VernacularTitle:DNA甲基转移酶抑制剂SGI-1027对人肝细胞癌细胞增殖及凋亡的影响
- Author:
Ning SUN
1
;
Jialin ZHANG
;
Chengshuo ZHANG
;
Ao JIAO
;
Baomin CHEN
Author Information
1. 中国医科大学附属第一医院肝胆外科暨器官移植科
- Keywords:
DNA methylation;
DNA methyltransferase inhibitor;
SGI-1027;
hepatocellular carcinoma
- From:
Journal of China Medical University
2017;46(9):807-811
- CountryChina
- Language:Chinese
-
Abstract:
Objective To elucidate the inhibitory effect of SGI-1027 on cell proliferation and apoptosis of Huh7 cells.Methods Huh7 cells were treated with different concentrations (0,5,10,15,20,25,30,and 35 μ mol/L) of SGI-1027 for 24 h.MTS assay was performed to detect cell proliferation.Huh7 cells treated with 0.1％ DMSO were used as the control group,and those treated with 30 μmol/L SGI-1027 as the experimental group.Flow cytometry was performed to study the cell cycle,and Annexin V-FITC/PI detection for studying cell apoptosis.TUNEL staining was performed to observe changes in cell morphology.Results The results of the MTS assay revealed that SGI-1027 significantly inhibited the proliferation of Huh7 cells in a dose-dependent manner,and the IC50 was 27.3 μmol/L.SGI-1027 did not block the cell cycle of Huh7 cells,but induced cell apoptosis in Huh7 cells.The rates of apoptosis were 3.242％ ± 0.204％ in the control group and 46.57％ ± 2.512％ in the experimental group (P ＜ 0.05).In the experimental group,typical apoptotic nucleus alterations were observed by fluorescence microscopy after TUNEL staining.The percentage of apoptotic cells was 1.077％ ± 0.407％ in the control group and 58.24％ ± 8.427％ in the experimental group (P ＜ 0.05).Condusion SGI-1027 inhibits Huh7 cell proliferation and induces apoptosis in vitro.
