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Effects of HDAC Inhibitor Scriptaid on IM9 Cell Line and Its Mechanism / 中国实验血液学杂志
Journal of Experimental Hematology ; (6): 1116-1121, 2018.
Article de Zh | WPRIM | ID: wpr-689519
Bibliothèque responsable: WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To study the effect of HDAC inhibitor Scriptaid on multiple myeloma IM9 cells and preliminarily clarify the mechanism of Scriptaid-induced cell apoptosis.</p><p><b>METHODS</b>The cell viability, cell cycle and cell apoptosis were measured by CCK8 assay and flow cytometry respectively, the relative target gene expression levels were detected by RT-PCR, the effect of Scriptaid on p21 promoter activity was detected by using luciferase reporter assay.</p><p><b>RESULTS</b>Scriptaid inhibited IM9 cell viability in a dose-dependent manner. Scriptaid induced IM9 cell cycle arrest at G/M phase in a dose-dependent manner. Scriptaid triggered IM9 cell apoptosis was obviously, the mRNA levels of apoptosis-related proteins Caspase 9, Caspase 3 and PARP1 were also activated. The apoptosis-associated factors BAD, PTEN and p21 increased following treatment with different dose of Scriptaid, meanwhile, p21 promoter activity was also activated significantly.</p><p><b>CONCLUSION</b>HDAC inhibitor Scriptaid can promote IM9 cell apoptosis by transcriptional activation of p21 promoter in concentration-dependent manner.</p>
Sujet(s)
Texte intégral: 1 Indice: WPRIM Sujet Principal: Pharmacologie / Quinoléines / Cycle cellulaire / Apoptose / Lignée cellulaire tumorale / Prolifération cellulaire / Inhibiteur p21 de kinase cycline-dépendante / Inhibiteurs de désacétylase d'histone / Hydroxylamines Limites du sujet: Humans langue: Zh Texte intégral: Journal of Experimental Hematology Année: 2018 Type: Article
Texte intégral: 1 Indice: WPRIM Sujet Principal: Pharmacologie / Quinoléines / Cycle cellulaire / Apoptose / Lignée cellulaire tumorale / Prolifération cellulaire / Inhibiteur p21 de kinase cycline-dépendante / Inhibiteurs de désacétylase d'histone / Hydroxylamines Limites du sujet: Humans langue: Zh Texte intégral: Journal of Experimental Hematology Année: 2018 Type: Article