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Phenotypic alterations of small cell lung carcinoma induced by different levels of wild-type p53 expression.
Adachi, J; Ookawa, K; Kohno, T; Tomizawa, Y; Tsuchida, S; Yokota, J.
Afiliación
  • Adachi J; Biology Division, National Cancer Center Research Institute, 1-1, Tsukiji 5-chome, Chuo-ku, Tokyo 104.
Cell Death Differ ; 5(2): 148-55, 1998 Feb.
Article en En | MEDLINE | ID: mdl-10200459
ABSTRACT
p53 induces both growth arrest and apoptosis in cancer cells. To clarify whether the level of p53 expression determines the response of small cell lung carcinoma (SCLC) cells, we assessed the effect of various p53 levels on a p53-null SCLC cell line, N417, using a tetracycline (Tc)-regulated inducible p53 expression system. Apoptosis was induced in SCLC cells with high p53 expression. Although low levels of p53 induced G1 arrest accompanied by p21 expression, cells with G1 arrest seemed to undergo apoptosis after further cultivation. Expression of exogenous p21 induced G1 arrest but not apoptosis in SCLC cells, suggesting that p53-mediated G1 arrest was induced through p21 expression. Moreover, high level of p53 expression down-regulated Bcl-2 expression in SCLC cells, while Bax was consistently expressed irrespective to the level of p53 expression. These results suggest that p53-mediated apoptosis and G1 arrest depend on level of p53 expression in SCLC cells and that the relative dominancy of Bax to Bcl-2 is involved in the induction of apoptosis by high level of p53 expression.
Asunto(s)
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Banco de datos: MEDLINE Asunto principal: Regulación Neoplásica de la Expresión Génica / Proteína p53 Supresora de Tumor / Apoptosis / Carcinoma de Células Pequeñas / Neoplasias Pulmonares Límite: Humans Idioma: En Revista: Cell Death Differ Año: 1998 Tipo del documento: Article
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Banco de datos: MEDLINE Asunto principal: Regulación Neoplásica de la Expresión Génica / Proteína p53 Supresora de Tumor / Apoptosis / Carcinoma de Células Pequeñas / Neoplasias Pulmonares Límite: Humans Idioma: En Revista: Cell Death Differ Año: 1998 Tipo del documento: Article