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Mitogen-activated protein kinase-dependent apoptosis in norcan-tharidin-treated A375-S2 cells is proceeded by the activation of protein kinase C / 中华医学杂志(英文版)
Chinese Medical Journal ; (24): 198-203, 2005.
Artículo en Inglés | WPRIM | ID: wpr-257299
ABSTRACT
<p><b>BACKGROUND</b>We have reported that norcantharidin (NCTD) induces human melanoma A375-S2 cell apoptosis and that the activation of caspase and the mitochondrial pathway are involved in the apoptotic process. This study aimed at investigating the roles of mitogen-activated protein kinase (MAPK) and protein kinase C (PKC) in A375-S2 cell apoptosis induced by NCTD.</p><p><b>METHODS</b>We assessed the effects of NCTD on cell growth inhibition using the 3-(4,5-dimethylthiazol-2-yl)-2,5-dipheyltetrazolium bromide (MTT) assay, DNA fragmentation (DNA agarose gel electrophoresis), and MAPK protein levels (Western blot analysis) in A375-S2 cells. Photomicroscopic data were also collected.</p><p><b>RESULTS</b>The NCTD inhibitory effect on A375-S2 cells was partially reversed by MAPK and PKC inhibitors. The expression of phosphorylated JNK and p38 also increased after the treatment with NCTD, and inhibitors of c-Jun NH2-terminal kinase (JNK) and p38 (SP600125 and SB203580, respectively) had significant inhibitory effects on the upregulation of phosphorylated JNK and p38 expression. Simultaneously, the PKC inhibitor staurosporine blocked the upregulation of phosphorylated JNK and phosphorylated p38, but had little effect on extracellular signal-regulated kinase (ERK) expression.</p><p><b>CONCLUSION</b>These results suggest that the activation of JNK and p38 MAPK promotes the process of NCTD-induced A375-S2 cell apoptosis and that PKC plays an important regulation role in the activation of MAPKs.</p>
Asunto(s)
Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Patología / Farmacología / Fisiología / Proteína Quinasa C / Apoptosis / Compuestos Bicíclicos Heterocíclicos con Puentes / Estaurosporina / Proteínas Quinasas Activadas por Mitógenos / Línea Celular Tumoral / Quimioterapia Límite: Humanos Idioma: Inglés Revista: Chinese Medical Journal Año: 2005 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Patología / Farmacología / Fisiología / Proteína Quinasa C / Apoptosis / Compuestos Bicíclicos Heterocíclicos con Puentes / Estaurosporina / Proteínas Quinasas Activadas por Mitógenos / Línea Celular Tumoral / Quimioterapia Límite: Humanos Idioma: Inglés Revista: Chinese Medical Journal Año: 2005 Tipo del documento: Artículo