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Effects of honokiol on the proliferation and apoptosis of human acute leukemia U937 cells / 国际肿瘤学杂志
Journal of International Oncology ; (12): 797-800, 2012.
Article Dans Chinois | WPRIM | ID: wpr-419416
ABSTRACT
ObjectiveTo detect the mechanism of the growth inhibition and apoptosis of human acute leukemia cell line U937 cells induced by honokiol.MethedsThe proliferation inhibition was detected by MTT method.Cell apoptosis was tested by Hoechst 33342 staining and flow cytometry with Annexin V/PI staining.RT-PCR was used to detect the mRNA expression of the apoptosis gene Bcl-2,Bax,Caspase 3,Caspase 8 and Caspase 9.ResultsThe inhibition effect of honokiol(5 μg/ml,48 h) on U937 cells proliferation could he observed,and the inhibition rate of 10 μg/ml honokiol on cell proliferation reached above 50% (48 h).U937 cells proliferation could be completely inhibited for 120 h. U937 cells apoptosis rate reached 26.8% (P <0.01)after being treated with 10 μg/ml honokiol.After being treated with 10 μg/ml honokiol for 48 h,the Bcl-2 gene expression in U937 cells was reduced (control group0.33 ± 0.02,experimental group0.14 ±0.01,P < 0.01 ),and the Bax gene expression was elevated ( control group0.1 ± 0.01,experimental group0.87 ± 0.08,P < 0.01 ).The gene expressions of Caspase 3 ( control group0.48 ± 0.01,experimental group0.87±0.06,P <0.01),Caspase 8(control group0.23±0.02,experimental group0.41 ±0.07,P < 0.01 ) and Caspase 9 ( control group0.44 ± 0.05,experimental group0.76 ± 0.06,P < 0.01 ) were all increased.The activity of Caspase-3 was 0.325 ±0.089,which was significantly higher than that of the control group ( P <0.01 ).ConclusionHonokiol can significantly inhibit the proliferation and induce cell apoptosis of human acute leukemia cell line U937 cells.The mechanism is related to the up-regulation of Bax and down-regulation of Bcl-2,and the endogenous and exogenous pathways are both inolved in the apoptosis process.

Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) langue: Chinois Texte intégral: Journal of International Oncology Année: 2012 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) langue: Chinois Texte intégral: Journal of International Oncology Année: 2012 Type: Article