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Indole-3-carbinol enhances ultraviolet B-induced apoptosis.by sensitizing human melanoma cells

Authors
Kim, D-S.Jeong, Y-M.Moon, S-I.Kim, S-Y.Kwon, S-B.Park, E-S.Youn, S-WPark, K-C
Issue Date
Nov-2006
Publisher
BIRKHAUSER VERLAG AG
Keywords
ultraviolet B; indole-3-carbinol; melanoma; apoptosis; cancer
Citation
CELLULAR AND MOLECULAR LIFE SCIENCES, v.63, no.22, pp 2661 - 2668
Pages
8
Journal Title
CELLULAR AND MOLECULAR LIFE SCIENCES
Volume
63
Number
22
Start Page
2661
End Page
2668
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/24255
DOI
10.1007/s00018-006-6306-1
ISSN
1420-682X
1420-9071
Abstract
Indole-3-carbinol (13C) has been found to act against several types of cancer, while ultraviolet B (UVB) is known to induce the apoptosis of human melanoma cells. Here, we investigated whether 13C can sensitize G361 human melanoma cells to UVB-induced apoptosis. We examined the effects of combined 13C and UVB (13C/UVB) at various dosages. 13C (200 mu M)/UVB (50 mJ/cm(2)) synergistically reduced melanoma cell viability, whereas 13C (200 mu M) or UVB (50 MJ/cm(2)), separately, had little effect on cell viability DNA fragmentation assays indicated that 13C/UVB induced apoptosis. Further results show that 13C/UVB activates caspase-8, -3, and Bid and causes the cleavage of poly(ADP-ribose) polymerase. Moreover, 13C decreased the expression of the anti-apoptotic protein, Bcl-2, whereas UVB increased the translocation of Bax to mitochondria. Thus, an increased Bax/Bcl-2 ratio by 13C/UVB may result in melanoma apoptosis. In conclusion, our study demonstrated that 13C sensitizes human melanoma cells by down-regulating Bcl-2.
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