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Reversal effect of gambogic acid on multidrug resistance of K562/A02 cell line / 中国实验血液学杂志
Journal of Experimental Hematology ; (6): 252-257, 2012.
Artigo em Chinês | WPRIM | ID: wpr-330980
ABSTRACT
This study was purposed to investigate the reversal effect of gambogic acid (GA) on multidrug resistance of K562/A02 cells and its mechanism. The IC(50) (half maximal inhibitory concentration) of adriamycin (ADM) was evaluated by MTT. Cell apoptosis was detected by flow cytometry. Morphological changes of K562/A02 cells were observed by fluorescent microscopy with DAPI staining. The expressions of Survivin and P-gp were determined by Western blot. The results showed that the IC(50) of ADM on K562 and K562/A02 cell proliferation were (1.42 ± 0.07) µg/ml and (28.42 ± 1.40) µg/ml respectively. GA ≤ 0.0625 µmol/L had no inhibitory effect on proliferation of K562 and K562/A02. 0.0625 µmol/L GA could enhance the sensitivity of K562/A02 cells to ADM (P < 0.05) and the reversal multiples was 1.53. The apoptotic rate was raised after treating with ADM combined with 0.0625 µmol/L GA for 48 h (P < 0.05). Morphological differences were typical and obvious between cells of control and treated groups under fluorescence microscopy using DAPI staining. After treating K562/A02 cells with ADM combined with 0.0625 µmol/L GA for 48 h, the expressions of Survivin and P-gp were down-regulated at protein levels. It is concluded that GA can enhance the sensitivity of K562/A02 cells to ADM, which may be related to increasing cell apoptosis and down-regulating expressions of Survivin and P-gp.
Assuntos
Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Farmacologia / Doxorrubicina / Substância P / Regulação Leucêmica da Expressão Gênica / Apoptose / Resistência a Múltiplos Medicamentos / Resistencia a Medicamentos Antineoplásicos / Células K562 / Xantonas / Proteínas Inibidoras de Apoptose Limite: Humanos Idioma: Chinês Revista: Journal of Experimental Hematology Ano de publicação: 2012 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Farmacologia / Doxorrubicina / Substância P / Regulação Leucêmica da Expressão Gênica / Apoptose / Resistência a Múltiplos Medicamentos / Resistencia a Medicamentos Antineoplásicos / Células K562 / Xantonas / Proteínas Inibidoras de Apoptose Limite: Humanos Idioma: Chinês Revista: Journal of Experimental Hematology Ano de publicação: 2012 Tipo de documento: Artigo