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Effect of valproic acid on apoptosis of leukemia HL-60 cells and expression of h-tert gene / 中国实验血液学杂志
Journal of Experimental Hematology ; (6): 1445-1450, 2010.
Article in Chinese | WPRIM | ID: wpr-332341
ABSTRACT
This study was aimed to clarify whether valproic acid (VPA) induces apoptosis of leukemia HL-60 cell line and its possible mechanism. The effect of different concentrations and treatment time of VPA on HL-60 cell proliferation was assayed by cytotoxicity test (CCK-8 method) and fluorescence microscopy, and flow cytometry was used to detect cell apoptosis. The expressions of telomerase subunit h-tert mRNA and apoptosis-related protein as well as caspase-3 activity were detected by real time-quantitative PCR, Western blot and ELISA respectively. The results indicated that VPA inhibited proliferation of HL-60 cells and induced cell apoptosis in a dose dependent manner (r = -0.87). The expressions of anti-apoptotic protein BCL-2 and h-tert mRNA were significantly decreased while the pro-apoptotic protein BAX and caspase-3 activity increased after treatment with VPA. The apoptosis rate of HL-60 cell was negatively correlated with expression of h-tert mRNA. It is concluded that VPA can inhibit leukemia HL-60 cell proliferation and induce apoptosis. The VPA displays anti-leukemia activity possibly through reducing h-tert mRNA and BCL-2 protein expression, increasing BAX expression and activity of caspase-3.
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Pharmacology / Valproic Acid / Apoptosis / Telomerase / HL-60 Cells / Proto-Oncogene Proteins c-bcl-2 / Bcl-2-Associated X Protein / Caspase 3 / Metabolism Limits: Humans Language: Chinese Journal: Journal of Experimental Hematology Year: 2010 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pharmacology / Valproic Acid / Apoptosis / Telomerase / HL-60 Cells / Proto-Oncogene Proteins c-bcl-2 / Bcl-2-Associated X Protein / Caspase 3 / Metabolism Limits: Humans Language: Chinese Journal: Journal of Experimental Hematology Year: 2010 Type: Article