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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.
Artículo en Chino | WPRIM | ID: wpr-689519
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>
Asunto(s)
Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Farmacología / Quinolinas / Ciclo Celular / Apoptosis / Línea Celular Tumoral / Proliferación Celular / Inhibidor p21 de las Quinasas Dependientes de la Ciclina / Inhibidores de Histona Desacetilasas / Hidroxilaminas Límite: Humanos Idioma: Chino Revista: Journal of Experimental Hematology Año: 2018 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Farmacología / Quinolinas / Ciclo Celular / Apoptosis / Línea Celular Tumoral / Proliferación Celular / Inhibidor p21 de las Quinasas Dependientes de la Ciclina / Inhibidores de Histona Desacetilasas / Hidroxilaminas Límite: Humanos Idioma: Chino Revista: Journal of Experimental Hematology Año: 2018 Tipo del documento: Artículo