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Role of prosurvival molecules in the action of lidamycin toward human tumor cells / 生物医学与环境科学(英文)
Biomedical and Environmental Sciences ; (12): 244-252, 2009.
Artículo en Inglés | WPRIM | ID: wpr-360669
ABSTRACT
<p><b>OBJECTIVE</b>Lidamycin, an enediyne antibiotic, leads to apoptosis and mitotic cell death of human tumor cells at high and low concentrations. The reason why tumor cells have distinct responses to lidamycin remains elusive. This study was to elucidate if cellular prosurvival molecules are involved in these responses.</p><p><b>METHODS</b>Cleavage of chromatin and DNA was observed by chromatin condensation and agarose gel electrophoresis. Accumulation of rhodamine 123 in lidamycin-treated cells was assayed by flow cytometry. Cell multinucleation was detected by staining with Hoechst 33342. Western blot and senescence-associated beta-galactosidase (SA-beta-gal) staining were used to analyze protein expression and senescence-like phenotype, respectively.</p><p><b>RESULTS</b>SIRT1 deacetylase remained unchanged in 0.5 nmol/L lidamycin whereas cleavage occurred when apoptosis was induced by lidamycin. Increased FOXO3a, SOD-1 and SOD-2 expression and transient phosphorylation of ERK were detected after exposure of human hepatoma BEL-7402 cells to 0.5 nmol/L lidamycin. High expressions of SIRT1 and Akt were found in colon carcinoma HCT116 p53 knock-out cells exposed to lidamycin. Degradation of PARP and p53 by lidamycin as a substitute for SIRT1 and Akt was confirmed with caspase inhibitor Q-VD-OPh and proteasome inhibitor MG132. Resistance to lidamycin-induced DNA cleavage was observed in breast cancer doxorubicin-resistant MCF-7 cells. This was not induced by P-glycoprotein as no accumulation of rhodamine 123 was detected in the resistant cells following exposure to lidamycin. In contrast to sensitive MCF-7 cells, a lower multinucleation rate for the resistant cells was measured following exposure to equal concentrations of lidamycin.</p><p><b>CONCLUSIONS</b>Cellular prosurvival molecules, such as SIRT1, Akt, SOD-1, SOD-2 and other unknown factors can influence the action of lidamycin on human tumor cells.</p>
Asunto(s)
Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Farmacología / Transducción de Señal / Doxorrubicina / Regulación de la Expresión Génica / Proteína p53 Supresora de Tumor / Muerte Celular / Poli(ADP-Ribosa) Polimerasas / Quinasas de Proteína Quinasa Activadas por Mitógenos / Sirtuinas / Línea Celular Tumoral Límite: Humanos Idioma: Inglés Revista: Biomedical and Environmental Sciences Año: 2009 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Farmacología / Transducción de Señal / Doxorrubicina / Regulación de la Expresión Génica / Proteína p53 Supresora de Tumor / Muerte Celular / Poli(ADP-Ribosa) Polimerasas / Quinasas de Proteína Quinasa Activadas por Mitógenos / Sirtuinas / Línea Celular Tumoral Límite: Humanos Idioma: Inglés Revista: Biomedical and Environmental Sciences Año: 2009 Tipo del documento: Artículo