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Apoptosis induced by diacetyldianhydrogalactitol and its mechanism in HL-60 leukemia cells / 药学学报
Acta Pharmaceutica Sinica ; (12): 691-695, 2002.
Article en Zh | WPRIM | ID: wpr-312035
Biblioteca responsable: WPRO
ABSTRACT
<p><b>AIM</b>To investigate the apoptosis induced by diacetyldianhydrogalactitol (DADAG) and its mechanism in human HL-60 leukemia cells.</p><p><b>METHODS</b>Inhibition of proliferation was measured by MTT assay. DADAG-induced apoptosis in HL-60 cells was observed by electron microscopy, flow cytometry and DNA fragmentation assay. The levels of Bcl-2 family proteins were detected by Western blotting. Caspase-3 activity was determined by ApoAlert CPP32 colorimetric assay kit.</p><p><b>RESULTS</b>DADAG exhibited potent antiproliferative activity and induced apoptosis in HL-60 cells. After treatment with DADAG 8 micrograms.mL-1 for various times, the Bcl-XL protein level decreased in a time-dependent manner, while the Bad protein level was upregulated. The caspase-3 activity increased markedly after treatment with DADAG for 24 h. The apoptotic signals were suppressed by z-VAD.fmk (a general inhibitor of caspases), whereas z-DEVD.fmk, a selective inhibitor of caspase-3, only induced partial reversion of the apoptotic effects.</p><p><b>CONCLUSION</b>DADAG-induced apoptosis in HL-60 cells required caspase-3 activation and caspase-3 activation was related with Bcl-2 family members.</p>
Asunto(s)
Texto completo: 1 Base de datos: WPRIM Asunto principal: Farmacología / División Celular / Apoptosis / Células HL-60 / Proteínas Proto-Oncogénicas c-bcl-2 / Caspasas / Dianhidrogalactitol / Proteína bcl-X / Caspasa 3 / Metabolismo Límite: Humans Idioma: Zh Revista: Acta Pharmaceutica Sinica Año: 2002 Tipo del documento: Article
Texto completo: 1 Base de datos: WPRIM Asunto principal: Farmacología / División Celular / Apoptosis / Células HL-60 / Proteínas Proto-Oncogénicas c-bcl-2 / Caspasas / Dianhidrogalactitol / Proteína bcl-X / Caspasa 3 / Metabolismo Límite: Humans Idioma: Zh Revista: Acta Pharmaceutica Sinica Año: 2002 Tipo del documento: Article