2010Linchuang huicuiRequires access

Effect of simvastatin and valproic acid on apoptosis and proliferation of K562 cells

LU De-yan

Open publisher page 0 citations

Abstract

Objective To investigate the effect of simvastatin and valproic acid(VPA) on the apoptosis and proliferation of K562 cells and its mechanism.Methods There were three groups in the experiment,srmvastatin,VPA simvastatin+VAP;with equalvolyme RPMI-1640 medium for the blank control group.The morphologic changes of K562 cells induced by simvastatin and VPA were observed under light microscopy with Wright-Giemsa staining.The cell proliferation was detected by MTT assay.The cell apoptosis ratio was detected by flow cytometry with labeling of AnnexinⅤ-FITC/PI.Results As compared with control group,after treatment with simvastatin 10,20,40 μmol/L,the apoptotic ratio at 48 h increased by(17.36±1.91)%,(23.26±2.35)%,(34.15±2.54)%;the apoptotic ratio at 72 hours increased by(31.43±2.15)%,(49.42±1.05)%,(56.57±3.06)%.After treatment with VPA 1,2,4 mmol/L,the apoptotic ratio at 48 hours increased by(14.30±1.39)%,(22.90±2.35)%,(39.79±2.65)%;the apoptotic ratio at 72 hours increased by(22.79±2.31)%,(34.67±2.78)%,(49.51±2.37)%.The apoptotic ratio was in time and dose-dependent manner.Conclusion Simvastatin and VPA may exert growth inhibition and apoptosis induction on K562 cells.There are increasing effects while treating with combination of simvastatin and VPA.

About this research paper

What this paper is about

Objective To investigate the effect of simvastatin and valproic acid(VPA) on the apoptosis and proliferation of K562 cells and its mechanism.Methods There were three groups in the experiment,srmvastatin,VPA simvastatin+VAP;with equalvolyme RPMI-1640 medium for the blank control group.The morphologic changes of K562 cells induced by simvastatin and VPA were observed under light microscopy with Wright-Giemsa staining.The cell proliferation was detected by MTT assay.The cell apoptosis ratio was detected by flow cytometry with labeling of AnnexinⅤ-FITC/PI.Results As compared with control group,after treatment with simvastatin 10,20,40 μmol/L,the apoptotic ratio at 48 h increased by(17.36±1.91)%,(23.26±2.35)%,(34.15±2.54)%;the apoptotic ratio at 72 hours increased by(31.43±2.15)%,(49.42±1.05)%,(56.57±3.06)%.After treatment with VPA 1,2,4 mmol/L,the apoptotic ratio at 48 hours increased by(14.30±1.39)%,(22.90±2.35)%,(39.79±2.65)%;the apoptotic ratio at 72 hours increased by(22.79±2.31)%,(34.67±2.78)%,(49.51±2.37)%.The apoptotic ratio was in time and dose-dependent manner.Conclusion Simvastatin and VPA may exert growth inhibition and apoptosis induction on K562 cells.There are increasing effects while treating with combination of simvastatin and VPA.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Objective To investigate the effect of simvastatin and valproic acid(VPA) on the apoptosis and proliferation of K562 cells and its mechanism.Methods There were three groups in the experiment,srmvastatin,VPA simvastatin+VAP;with equalvolyme RPMI-1640 medium for the blank control group.The morphologic changes of K562 cells induced by simvastatin and VPA were observed under light microscopy with Wright-Giemsa staining.The cell proliferation was detected by MTT assay.The cell apoptosis ratio was detected by flow cytometry with labeling of AnnexinⅤ-FITC/PI.Results As compared with control group,after treatment with simvastatin 10,20,40 μmol/L,the apoptotic ratio at 48 h increased by(17.36±1.91)%,(23.26±2.35)%,(34.15±2.54)%;the apoptotic ratio at 72 hours increased by(31.43±2.15)%,(49.42±1.05)%,(56.57±3.06)%.After treatment with VPA 1,2,4 mmol/L,the apoptotic ratio at 48 hours increased by(14.30±1.39)%,(22.90±2.35)%,(39.79±2.65)%;the apoptotic ratio at 72 hours increased by(22.79±2.31)%,(34.67±2.78)%,(49.51±2.37)%.The apoptotic ratio was in time and dose-dependent manner.Conclusion Simvastatin and VPA may exert growth inhibition and apoptosis induction on K562 cells.There are increasing effects while treating with combination of simvastatin and VPA.

Key concepts: Simvastatin, Apoptosis, Annexin, Medicine, Valproic Acid, Flow cytometry, MTT assay, K562 cells

Related papers

Back to paper searchBrowse research topicsOriginal source
Effect of simvastatin and valproic acid on apoptosis and proliferation of K562 cells — Research Paper | ScholarLens