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Reversed effect of valproic acid on transcription inhibition of AML1-ETO fusion protein of kasumi-1 leukemic cell line / 中国实验血液学杂志
Journal of Experimental Hematology ; (6): 363-367, 2009.
Article Dans Chinois | WPRIM | ID: wpr-302132
ABSTRACT
This study was aimed to investigate the mechanism of histone deacetylase (HDAC) inhibitor, valproic acid (VPA), reversing transcription inhibition of AML1-ETO fusion protein in Kasumi-1 cell line. The mRNA expressions of AML1-ETO, AML1 and cyclin D2 were detected by semi-quantitation RT-PCR after treating kasumi-1 cells with VPA at different doses/and different time points. The results indicated that the mRNA expression of AML1-ETO showed no obvious change, when kasumi-1 cells were treated with VPA. Compared with control group, the expression level of AML1 mRNA significantly increased in a dose-dependent manner. Compared with control group, the expression level of cyclin D2 mRNA significantly decreased when kasumi-1 cells had been treated with 3 mmol/L VPA as well as kasumi-1 cells were treated with different concentrations of VPA for 3 days. In conclusion, VPA could remove transcription inhibition of AML1-ETO fusion protein, increase transcription of AML1 and down-regulate mRNA expression of AML1 target gene cyclin D2 through HDAC inhibiting activity.
Sujets)
Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Pharmacologie / Acétylation / Histone / Régulation de l'expression des gènes dans la leucémie / Protéines de fusion oncogènes / Acide valproïque / Lignée cellulaire tumorale / Sous-unité alpha 2 du facteur CBF / Cycline D2 / Inhibiteurs de désacétylase d'histone Limites du sujet: Humains langue: Chinois Texte intégral: Journal of Experimental Hematology Année: 2009 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Pharmacologie / Acétylation / Histone / Régulation de l'expression des gènes dans la leucémie / Protéines de fusion oncogènes / Acide valproïque / Lignée cellulaire tumorale / Sous-unité alpha 2 du facteur CBF / Cycline D2 / Inhibiteurs de désacétylase d'histone Limites du sujet: Humains langue: Chinois Texte intégral: Journal of Experimental Hematology Année: 2009 Type: Article