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Orphanin FQ combined with adriamycin reverses multi-drug resistance of K562/ADM and its molecular mechanism / 中国实验血液学杂志
Journal of Experimental Hematology ; (6): 574-578, 2012.
Artigo em Chinês | WPRIM | ID: wpr-263347
ABSTRACT
Our study have confirmed that orphanin FQ (OFQ) alone can reverse the multi-drug resistance of K562/ADM at the cellular level. Thus, this study was purposed to investigate the molecular mechanism of OFQ combined with ADM that reverses multi-drug resistance of K562/ADM, as well as its correlation with the expression of MDR1 mRNA and P-glycoprotein (P-gp). MTT method was used to detect the proliferation ability of K562/ADM treated with OFQ and ADM alone and their combination; flow cytometry was performed to measure the cell apoptosis rate; real time-PCR was applied to detect the MDR1 mRAN expression; Western blot was used to determine the P-gp expression. The results showed that OFQ (0.1 µmol/L) combined with ADM (15 mg/L) significantly inhibited the cell proliferation of K562/ADM, compared with ADM group; the date gained at 48 h was statistically significant (P < 0.05), and cell apoptosis rate was significantly raised (P < 0.01); MDR1 mRNA and P-gp expression levels of OFR combined with ADM were significantly lower than that of ADM alone, and were time-dependent within 48 h. It is concluded that OFQ combined with ADM can reverse the multi-drug resistance of K562/ADM in time-dependent manner, and the 48 h after treatment with these 2 drugs is the best reverse time, which may be related with down regulating the expression of MDR1 mRNA and P-gp.
Assuntos
Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Farmacologia / Doxorrubicina / Membro 1 da Subfamília B de Cassetes de Ligação de ATP / Peptídeos Opioides / Resistência a Múltiplos Medicamentos / Resistencia a Medicamentos Antineoplásicos / Subfamília B de Transportador de Cassetes de Ligação de ATP / Células K562 / Metabolismo 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 / Membro 1 da Subfamília B de Cassetes de Ligação de ATP / Peptídeos Opioides / Resistência a Múltiplos Medicamentos / Resistencia a Medicamentos Antineoplásicos / Subfamília B de Transportador de Cassetes de Ligação de ATP / Células K562 / Metabolismo Limite: Humanos Idioma: Chinês Revista: Journal of Experimental Hematology Ano de publicação: 2012 Tipo de documento: Artigo