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The interaction between the light source dose and caspase-dependent and -independent apoptosis in human SK-MEL-3 skin cancer cells following photodynamic therapy with zinc phthalocyanine: A comparative study.
- Source :
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Journal of Photochemistry & Photobiology B: Biology . Nov2017, Vol. 176, p62-68. 7p. - Publication Year :
- 2017
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Abstract
- The aim of this study is to determine the behavior of relative expression of Bcl-2, caspase-8, caspase-9, and caspase-3 genes of/in SK-MEL-3 cancer cells and explore molecular mechanisms responsible for the apoptosis response during an in vitro photodynamic therapy (PDT) with Zinc Phthalocyanine (ZnPc) using different doses of the light source. In this study, firstly the cytotoxic effects of ZnPc-PDT on SK-MEL-3 cells were evaluated. By irradiating the laser, ZnPc induced a significant amount of apoptosis on SK-MEL-3 cells in three IC 50 s including 0.064 ± 0.01, 0.043 ± 0.01, and 0.036 ± 0.01 μg/mL at the doses of 8, 16, and 24 J/cm 2 , respectively. Moreover, flow cytometry and QRT-PCR experiments were done. The high percentage of apoptotic cells was seen in the early apoptosis stage. The expression of Bcl-2 and caspase-8 genes at all doses of laser experienced an obvious reduction in comparison to the control group. On the other hand, although the expression of caspase-9 and caspase-3 genes remains almost constant at 8 J/cm 2 , but they faced an increment at 16 and 24 J/cm 2 doses. These data reveal caspase-dependent apoptosis in high and caspase-independent apoptosis in low doses of laser. Based on the results of present work, it can be suggested that the dose of the light source is a key factor in induction of caspase-dependent and caspase-independent apoptosis pathways following PDT. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 10111344
- Volume :
- 176
- Database :
- Academic Search Index
- Journal :
- Journal of Photochemistry & Photobiology B: Biology
- Publication Type :
- Academic Journal
- Accession number :
- 125722295
- Full Text :
- https://doi.org/10.1016/j.jphotobiol.2017.09.020