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Synthetic CDCA Derivatives-Induced Apoptosis of Stomach Cancer Cell Line SNU-1 Cells / Journal of the Korean Cancer Association, 대한암학회지
Cancer Research and Treatment ; : 132-139, 2004.
Artículo en Inglés | WPRIM | ID: wpr-162441
ABSTRACT

PURPOSE:

This study was conducted to explore whether CDCA derivatives induce apoptosis in a stomach cancer cell line, and to dissect the detailed mechanism underlying apoptosis. MATERIALS AND

METHODS:

The human stomach cancer cell line, SNU-1, cells were treated with the synthetic CDCA derivatives, HS-1199 and HS-1200. DNA and mitochondrial stains were used to detect apoptotic cells by fluorescence imaging or flow cytometry. The caspase-3 activity was measured by Western blotting.

RESULTS:

Both the HS-1199 and HS-1200 induced decreased viabilities of the SNU-1 cells, in time-dependent manners. The CDCA derivatives demonstrated various apoptosis hallmarks, such as mitochondrial changes reduction of MMP, cytochrome c release, and Smac/ DIABLO translocation), activation of caspase-3 (resulting in the degradation of PARP and DFF45), DNA fragmentation and nuclear condensation.

CONCLUSION:

The CDCA derivatives, HS-1199 and HS- 1200, both induced apoptosis of the SNU-1 gastric cancer cells in caspase- and mitochondria-dependent fashions. Many important issues relating to their therapeutic applications remain to be elucidated.
Asunto(s)

Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Estómago / Neoplasias Gástricas / ADN / Línea Celular / Ácido Quenodesoxicólico / Western Blotting / Apoptosis / Caspasas / Citocromos c / Colorantes Límite: Humanos Idioma: Inglés Revista: Cancer Research and Treatment Año: 2004 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Estómago / Neoplasias Gástricas / ADN / Línea Celular / Ácido Quenodesoxicólico / Western Blotting / Apoptosis / Caspasas / Citocromos c / Colorantes Límite: Humanos Idioma: Inglés Revista: Cancer Research and Treatment Año: 2004 Tipo del documento: Artículo