Summary.
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 IκB 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-κB activity and IL-18 expression in HPV-negative cervical cancer C-33A cells.
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Abbreviations
- IFN-γ:
-
interferon-γ
- FasL:
-
Fas ligand
- NF-κB:
-
nuclear facor-κB
- HPV:
-
human papillomavirus
- MMC:
-
mitomycin C
- CIS:
-
cisplatin
- CA:
-
carboplatin
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Kang, Y., Lee, KA., Yang, Y. et al. The apoptotic effect of intercalating agents on HPV-negative cervical cancer C-33A cells. Amino Acids 33, 105–112 (2007). https://doi.org/10.1007/s00726-006-0417-8
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DOI: https://doi.org/10.1007/s00726-006-0417-8