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Indole-3-carbinol enhances ultraviolet B-induced apoptosis by sensitizing human melanoma cells
Authors:D -S Kim  Y -M Jeong  S -I Moon  S -Y Kim  S -B Kwon  E -S Park  S -W Youn  K -C Park
Institution:(1) Department of Dermatology, Seoul National University Bundang Hospital, 300 Gumi-Dong, Bundang-Gu, Seongnam-Si, Gyeonggi-Do, 463–707, Korea;(2) College of Medicine, Chung-Ang University, Seoul, 156-756, Korea;(3) Welskin Co. Ltd, 28 Yongon-Dong, Chongno-Gu, Seoul, 110-744, Korea
Abstract:Indole-3-carbinol (I3C) 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 I3C can sensitize G361 human melanoma cells to UVB-induced apoptosis. We examined the effects of combined I3C and UVB (I3C/UVB) at various dosages. I3C (200 μM)/UVB (50 mJ/cm2) synergistically reduced melanoma cell viability, whereas I3C (200 μM) or UVB (50 mJ/cm2), separately, had little effect on cell viability. DNA fragmentation assays indicated that I3C/UVB induced apoptosis. Further results show that I3C/UVB activates caspase-8, −3, and Bid and causes the cleavage of poly(ADP-ribose) polymerase. Moreover, I3C 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 I3C/UVB may result in melanoma apoptosis. In conclusion, our study demonstrated that I3C sensitizes human melanoma cells by down-regulating Bcl-2. Received 5 July 2006; received after revision 25 August 2006; accepted 11 September 2006
Keywords:Ultraviolet B  indole-3-carbinol  melanoma  apoptosis  cancer
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