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Down-regulation of mTOR activity and survivin expression during tamoxifen-induced apoptosis in hepatoblastoma cells / 中华肿瘤杂志
Chinese Journal of Oncology ; (12): 903-906, 2010.
Artículo en Chino | WPRIM | ID: wpr-293456
ABSTRACT
<p><b>OBJECTIVE</b>The aim of this study was to investigate the changes in mTOR activity and survivin expression in liver cancer cell line HepG2 cells treated with tamoxifen.</p><p><b>METHODS</b>Survivin transcription level and p70S6K was demonstrated by PCR, dual-luciferase reporter assay and Western blot analysis, respectively, and the apoptosis in the HepG2 cells was detected by flow cytometry.</p><p><b>RESULTS</b>Tamoxifen leads to apoptosis of the cells and reduction in survivin expression, as well as a dramatic reduction in the activated form of p70S6K. Treating HepG2 cells with rapamycin, a specific mTOR inhibitor, significantly reduced the survivin protein level but not affected the survivin transcription, indicating that tamoxifen and rapamycin were synergistic in regards to down-regulation of survivin expression in hepatocellular carcinoma cells.</p><p><b>CONCLUSIONS</b>Our results suggest that tamoxifen down-regulates survivin expression in HepG2 cells and it is mediated by transcriptional and post-transcriptional level via PI3K/Akt/mTOR pathway to induce apoptosis.</p>
Asunto(s)
Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Farmacología / Tamoxifeno / ARN Mensajero / Transducción de Señal / Regulación hacia Abajo / Apoptosis / Antineoplásicos Hormonales / Fosfatidilinositol 3-Quinasas / Sirolimus / Proteínas Quinasas S6 Ribosómicas 70-kDa Límite: Humanos Idioma: Chino Revista: Chinese Journal of Oncology Año: 2010 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Farmacología / Tamoxifeno / ARN Mensajero / Transducción de Señal / Regulación hacia Abajo / Apoptosis / Antineoplásicos Hormonales / Fosfatidilinositol 3-Quinasas / Sirolimus / Proteínas Quinasas S6 Ribosómicas 70-kDa Límite: Humanos Idioma: Chino Revista: Chinese Journal of Oncology Año: 2010 Tipo del documento: Artículo