Paper
24 February 2009 Involvement of caspase-dependent and -independent apoptotic pathways in cisplatin-induced apoptosis
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Abstract
Cisplatin, an efficient anticancer agent, can trigger multiple apoptotic pathways in cancer cells. However, the signal transduction pathways in response to cisplatin-based chemotherapy are complicated, and the mechanism is not fully understood. In current study, we showed that, during cisplatin-induced apoptosis of human lung adenocarcinoma cells, both the caspase-dependent and -independent pathways were activated. Herein, we reported that after cisplatin treatment, the activities of caspase-9/-3 were sharply increased; pre-treatment with Z-LEHD-fmk (inhibitor of caspase-9), Z-DEVD-fmk (inhibitor of caspase-3), and Z-VAD-fmk (a pan-caspase inhibitor) increased cell viability and decreased apoptosis, suggesting that caspase-mediated apoptotic pathway was activated following cisplatin treatment. Confocal imaging of the cells transfected with AIF-GFP demonstrated that AIF release occurred about 9 h after cisplatin treatment. The event proceeded progressively over time, coinciding with a nuclear translocation and lasting for more than 2 hours. Down-regulation of AIF by siRNA also significantly increased cell viability and decreased apoptosis, these results suggested that AIF-mediated caspase-independent apoptotic pathway was involved in cispatin-induced apoptosis. In conclusion, the current study demonstrated that both caspase-dependent and -independent apoptotic pathways were involved in cisplatin-induced apoptosis in human lung adenocarcinoma cells.
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Lei Liu, Yingjie Zhang, and Xianwang Wang "Involvement of caspase-dependent and -independent apoptotic pathways in cisplatin-induced apoptosis", Proc. SPIE 7178, Biophotonics and Immune Responses IV, 71780N (24 February 2009); https://doi.org/10.1117/12.808431
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KEYWORDS
Cell death

Proteins

Lung

Confocal microscopy

Luminescence

Cancer

Flow cytometry

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