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Amino Acids ; 33(1): 105-12, 2007 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-17021654

RESUMO

Cervical cancer is one of the leading causes of female cancer death worldwide with about 500,000 deaths per year. Both mitomycin C and cisplatin are alkylating agents, which bind and intercalate DNA, and thus used as anti-cancer drugs. In these studies, we focused on investigating the apoptotic effects of intercalating agents on HPV-negative cervical cancer C-33A cells. Accordingly, C-33A cells were treated with carboplatin, mitomycin C or cisplatin. Cell cycle analysis revealed that treatment with mitomycin C and cisplatin but not with carboplatin resulted in apoptosis. Both mitomycin C and cisplatin induced apoptosis in C-33A cells via caspase-8 and -3 processing in a Fas/FasL-dependent manner and also suppressed IL-18 expression, while they down-regulated IkappaB expression and up-regulated p65 expression. These results suggest that both mitomycin C and cisplatin induce apoptosis, not only via the caspase-8 and -3 dependent Fas/FasL pathway, but also via the regulation of NF-kappaB activity and IL-18 expression in HPV-negative cervical cancer C-33A cells.


Assuntos
Apoptose/efeitos dos fármacos , Caspases/metabolismo , Substâncias Intercalantes/farmacologia , Papillomaviridae , Neoplasias do Colo do Útero/patologia , Western Blotting , Carboplatina/farmacologia , Proliferação de Células/efeitos dos fármacos , Cisplatino/farmacologia , Ensaio de Imunoadsorção Enzimática , Proteína Ligante Fas/metabolismo , Feminino , Humanos , Interleucina-18/metabolismo , Mitomicina/farmacologia , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Células Tumorais Cultivadas , Neoplasias do Colo do Útero/metabolismo , Neoplasias do Colo do Útero/virologia , Receptor fas/metabolismo
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