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Mdr-1 ribozyme in the reversal of multidrug resistance in human ovarian cancer / 中华肿瘤杂志
Chinese Journal of Oncology ; (12): 425-428, 2003.
Artigo em Chinês | WPRIM | ID: wpr-347411
ABSTRACT
<p><b>OBJECTIVE</b>To study the mechanism of multidrug resistance and its reversal by mdr-1 ribozyme in human ovarian cancer.</p><p><b>METHODS</b>The expression of mdr-1 and p-glycoprotein (p-gp) was studied by confocal laser microscope (Confocal), RT-PCR and Western blot analysis in adriamycin-resistant human ovarian cancer cell line (A2780/ADM) and adriamycin-sensitive one (A2780). The mdr-1 ribozyme was transfected into the A2780/ADM by Lipofectamine 2000 to overcome the multidrug resistance in ovarian cancer.</p><p><b>RESULTS</b>The expression of mdr-1 mRNA and p-gp in A2780/ADM was significantly higher than that in A2780. The expression of mdr-1 mRNA and p-gp in A2780/ADM was lowered after being transfected by mdr-1 ribozyme.</p><p><b>CONCLUSION</b>Multidrug resistance of A2780/ADM, possibly being caused by overexpression of mdr-1 gene, can be partially reversed by mdr-1 ribozyme.</p>
Assuntos
Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Neoplasias Ovarianas / RNA Mensageiro / RNA Catalítico / Membro 1 da Subfamília B de Cassetes de Ligação de ATP / Resistência a Múltiplos Medicamentos / Resistencia a Medicamentos Antineoplásicos / Usos Terapêuticos / Tratamento Farmacológico / Genética / Metabolismo Limite: Feminino / Humanos Idioma: Chinês Revista: Chinese Journal of Oncology Ano de publicação: 2003 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Neoplasias Ovarianas / RNA Mensageiro / RNA Catalítico / Membro 1 da Subfamília B de Cassetes de Ligação de ATP / Resistência a Múltiplos Medicamentos / Resistencia a Medicamentos Antineoplásicos / Usos Terapêuticos / Tratamento Farmacológico / Genética / Metabolismo Limite: Feminino / Humanos Idioma: Chinês Revista: Chinese Journal of Oncology Ano de publicação: 2003 Tipo de documento: Artigo