Effects of Bufalin on Up-regulating Methylation of Wilm's Tumor 1 Gene in Human Erythroid Leukemic Cells

• 来源期刊: 中国结合医学杂志（英文版）
• 年，卷（期）: 2017,（4）
• 页码范围: 288-294
• 页数: 7页
• 语种: 英文
• DOI: 10.1007/s11655-017-2404-1

摘要

Objective:To explore the effects of bufalin on inhibiting proliferation,up-regulating methylation of Wilm'tumor 1 gene (WT1) as well as its possible mechanisms in human erythroid leukemic (HEL) cells.Methods:The HEL cells were treated with bufalin at various concentrations to observe cellular morphology,proliferation assay and cell cycle.The mRNA and protein expression levels of Wrl1 were detected by reverse transcription polymerase chain reaction (RT-PCR),Western blot and immunocytochemistry,DNA methylation of WT1 and protein expression levels of DNA methyltransferase 3a (DNMT3a) and DNMT3b were analyzed by methylation-specific PCR,and Westem blot respectively.Results:The bufalin was effective to inhibit proliferation of HEL cells in a dose-dependent manner,their suppression rates were from 23.4％±2.1％ to 87.2％±5.4％ with an half maximal inhibit concentration (IC50) of 0.046 μ mol/L.Typical apoptosis morphology was observed in bufalin-treated HEL cells.The proliferation index of cell cycle decreased from 76.4％± 1.9％ to 49.7％ ± 1.3％.The expression levels of WT1 mRNA and its protein reduced gradually with increasing doses of bufalin,meanwhile,the methylation status of WT1 gene changed from unmethylated into partially or totally methylated.While,the expression levels of DNMT3a and DNMT3b protein gradually increased by bufalin treatment in a dose-dependent manner.Conclusions:Bufalin can not only significantly inhibit the proliferation of HEL cells and arrest cell cycle at G0/G1 phase,but also induce cellular apoptosis and down-regulate the expression level of WT1.Our results provide the evidence of bufalin for anti-leukemia,its mechanism may involve in increasing WT1 methylation status which is related to the up-regulation of DNMT3a and DNMT3b proteins in enythroid leukemic HEL cells.