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Cancer Lett ; 151(1): 39-48, 2000 Apr 03.
Artículo en Inglés | MEDLINE | ID: mdl-10766421

RESUMEN

Ceramide acts as a mediator of apoptosis in various cell lines, but little is known regarding the molecular mechanism linked to the cell cycle. In the present study, we examined the expression of p27(kip1) and its relationship to apoptosis induced by ceramide. We demonstrated that treatment of HL-60 cells with C6-ceramide resulted in G1 phase elevation followed by apoptotic cleavage associated with increase in the level of cdk inhibitor p27(kip1). Ceramide inhibited the kinase activities of cdk2 and cdk4 within 24 h of treatment. Ceramide-induced inhibition of cdk2 and cdk4 kinase activities was accompanied by increase of p27(kip1) in the cdks complexes. In addition, we have shown that both the cell death and expression of p27(kip1) protein induced by ceramide were significantly decreased in HL-60 cells overexpressing bcl-2. Furthermore, ceramide induced a significant increase in Bax protein expression coincided with increase in p27(kip1) protein level. These findings indicate that p27(kip1) may play important roles in mediating ceramide-induced apoptosis and its expression can be regulated by Bax and Bcl-2.


Asunto(s)
Apoptosis/fisiología , Quinasas CDC2-CDC28 , Proteínas de Ciclo Celular , Ceramidas/farmacología , Quinasas Ciclina-Dependientes/antagonistas & inhibidores , Proteínas Asociadas a Microtúbulos/metabolismo , Proteínas Proto-Oncogénicas , Proteínas Supresoras de Tumor , Apoptosis/efectos de los fármacos , Ciclina D1/genética , Ciclina D1/metabolismo , Ciclina E/genética , Ciclina E/metabolismo , Quinasa 2 Dependiente de la Ciclina , Quinasa 4 Dependiente de la Ciclina , Inhibidor p27 de las Quinasas Dependientes de la Ciclina , Quinasas Ciclina-Dependientes/genética , Fase G1 , Regulación de la Expresión Génica/efectos de los fármacos , Células HL-60 , Humanos , Cinética , Proteínas Serina-Treonina Quinasas/antagonistas & inhibidores , Proteínas Serina-Treonina Quinasas/genética , Proteínas Proto-Oncogénicas c-bcl-2/metabolismo , ARN Mensajero/genética , Proteínas Recombinantes/metabolismo , Transcripción Genética/efectos de los fármacos , Transfección
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