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The mechanism of alteronol inhibiting the proliferation of human promyelocytic leukemia HL-60 cells / 药学学报
Acta Pharmaceutica Sinica ; (12): 1477-1482, 2012.
Article in Chinese | WPRIM | ID: wpr-274635
ABSTRACT
This study is to investigate the mechanism of human promyelocytic leukemia HL-60 cells proliferation induced by alteronol in vitro. Human promyelocytic leukemia HL-60 cells cultured in vitro were treated with different concentrations of alteronol. Inhibition rate was detected by SRB assay. Cellular morphological changes were observed by Hoechst and AO/EB (acridine orange/ethidium bromide dye) staining. The apoptosis rate was determined by Annexin V-FITC/PI assay. Cell cycle distribution was determined by flow cytometry. Western blotting analysis was carried out to determine the cell cycle related proteins. The proliferation of HL-60 cells treated with alteronol was inhibited in a concentration-dependent manner. Based on cell viability assay, observation on cell morphology and apoptosis rate, it confirmed that alteronol played an obvious role in proliferation inhibition of human promyelocytic leukemia HL-60 cells, but it did not induce apoptosis in human promyelocytic leukemia HL-60 cells in different concentrations groups. Alteronol could effectively inhibit the proliferation of human promyelocytic leukemia HL-60 cells inducing cell cycle arrest at G1 phase, as well as, alteration expression of cell cycle proteins level of CyclinD1 and pRb.
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Pharmacology / Phosphorylation / Cell Cycle / Retinoblastoma Protein / Naphthoquinones / Apoptosis / HL-60 Cells / Cyclin D1 / Cell Proliferation / Dose-Response Relationship, Drug Limits: Humans Language: Chinese Journal: Acta Pharmaceutica Sinica Year: 2012 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pharmacology / Phosphorylation / Cell Cycle / Retinoblastoma Protein / Naphthoquinones / Apoptosis / HL-60 Cells / Cyclin D1 / Cell Proliferation / Dose-Response Relationship, Drug Limits: Humans Language: Chinese Journal: Acta Pharmaceutica Sinica Year: 2012 Type: Article