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TRAIL-induced cell death and caspase-8 activation are inhibited by cisplatin but not carboplatin / 부인종양
Journal of Gynecologic Oncology ; : 113-116, 2009.
Artigo em Inglês | WPRIM | ID: wpr-111284
ABSTRACT

OBJECTIVE:

Platinum (Pt) based drugs including cisplatin and carboplatin are widely used as anticancer drugs in various human cancers. Many studies have shown that chemotherapeutic agents synergistically enhance cell death induced by death ligands. However it has been recently reported that cisplatin may inhibit tumor necrosis factor-related apoptosis-inducing ligand (TRAIL)-induced cell death through inactivation of caspases. Thus, we investigated whether carboplatin also inhibits TRAIL-induced cell death.

METHODS:

HeLa cells were treated with TRAIL in the presence of cisplatin or carboplatin, and cell death was analyzed using the crystal violet staining method. Caspase activation was checked through detection of Bid cleavage by Western blotting using anti-Bid antibody.

RESULTS:

Cisplatin inhibits TRAIL-induced cell death in HeLa cells; however, carboplatin enhanced TRAIL-induced cell death. Whereas cisplatin inhibited caspase-8-mediated Bid cleavage, carboplatin had no effect on caspase-8 activity.

CONCLUSION:

Although cisplatin and carboplatin are platinum-containing cancer therapeutic agents, they have the opposite effects on TRAIL-induced cell death.
Assuntos

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Platina / Células HeLa / Western Blotting / Carboplatina / Cisplatino / Morte Celular / Caspases / Caspase 8 / Violeta Genciana / Ligantes Limite: Humanos Idioma: Inglês Revista: Journal of Gynecologic Oncology Ano de publicação: 2009 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Platina / Células HeLa / Western Blotting / Carboplatina / Cisplatino / Morte Celular / Caspases / Caspase 8 / Violeta Genciana / Ligantes Limite: Humanos Idioma: Inglês Revista: Journal of Gynecologic Oncology Ano de publicação: 2009 Tipo de documento: Artigo