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Preliminary studies on the mechanisms of a new anti-tumor agent PH II-7 with special preference to multidrug resistant tumor cells / 中国医学科学院学报
Article en Zh | WPRIM | ID: wpr-350060
Biblioteca responsable: WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To determine the anti-tumor activity of PH II-7 in vitro and explore preliminarily its mechanisms.</p><p><b>METHODS</b>The anti-tumor activity was measured using colorimetric MTT assay. Apoptosis was determined with fluorescence-activated cell sorter (FACS), electron microscopy and agarose gel electrophoresis. The expressions of mdr1 and sorcin genes were determined by Northern blot assay.</p><p><b>RESULTS</b>PH II-7 inhibited the proliferation of various human tumor cells derived from different tumor cell lines. The IC50 values varied from 0.34-18.61 mumol/L. Especially, PH II-7 had strong inhibitory effect on multidrug resistant tumor cells, whereas adriamycin (ADR) was resistant. Apoptosis was induced in HL60 and HL60/ADR cells treated with 1 microgram/ml PH II-7, while PH II-7 inhibited the expressions of mdr1 and sorcin genes.</p><p><b>CONCLUSIONS</b>PH II-7 is a new potential agent which has strong inhibitory effect on both multidrug resistant cells and their parental cells. PH II-7 may increase the intracellular drug concentration in MDR cells by inhibiting the expressions of the MDR-related genes mdr1 and sorcin and induce the apoptosis of MDR cells and their parental tumor cells.</p>
Asunto(s)
Texto completo: 1 Base de datos: WPRIM Asunto principal: Farmacología / Medicamentos Herbarios Chinos / División Celular / Química / Apoptosis / Miembro 1 de la Subfamilia B de Casetes de Unión a ATP / Células HL-60 / Células K562 / Combinación de Medicamentos / Genética Aspecto: Patient_preference Límite: Humans Idioma: Zh Revista: Acta Academiae Medicinae Sinicae Año: 2002 Tipo del documento: Article
Texto completo: 1 Base de datos: WPRIM Asunto principal: Farmacología / Medicamentos Herbarios Chinos / División Celular / Química / Apoptosis / Miembro 1 de la Subfamilia B de Casetes de Unión a ATP / Células HL-60 / Células K562 / Combinación de Medicamentos / Genética Aspecto: Patient_preference Límite: Humans Idioma: Zh Revista: Acta Academiae Medicinae Sinicae Año: 2002 Tipo del documento: Article