Chemopreventive Effects of Sarcotriol on Ultraviolet B-induced Skin Tumor Development in SKH-1 Hairless Mice

Marine Drugs

Vipra Kundoor²  Xiaoying Zhang²  Ajay Bommareddy²  Sherief Khalifa¹  Hesham Fahmy² 

[1] Department of Pharmacognosy, Faculty of Pharmacy, Suez Canal University, Ismailia, Egypt;Department of Pharmaceutical Sciences, South Dakota State University, Box 2202C, Brookings, SD 57007, USA. Tel.: [phone], Fax [phone].

关键词: Cancer chemoprevention;    Skin cancer;    Cembranoids;    Sarcophine;    Sarcophyton glaucum;    Sarcotriol;    Apoptosis;    p53;   

DOI  :  10.3390/md504197

来源: mdpi

【 摘 要 】

Sarcotriol (ST) has been shown to be chemopreventive on 7,12-dimethyl-benz(a)anthracene (DMBA) initiated and 12-O-tetradecanoylphorbol-13-acetate (TPA)-promoted skin tumor development in CD-1 mice in recent studies from our laboratory. The objective of this study was to determine the chemopreventive effects of ST on ultraviolet B (UVB)-induced skin tumor development in female SKH-1 hairless mice, an experimental model relevant to human skin cancer development, and its possible mechanisms of action. Female SKH-1 mice were divided into two groups: Control and ST treated. Control was topically treated with 100 μL acetone and ST treated group administered with 30 μg ST in 100 μL acetone one hour before UVB exposure. For UVB-induced tumorigenesis, carcinogenesis was initiated and promoted by UVB (180 mJ/cm²). Group weights and tumor counts were taken once every week. After 30 weeks, mice were sacrificed and dorsal skin samples were collected. The proteins from the skin sample were further used for SDS-PAGE and Western blotting using specific antibodies against caspase-3, caspase-8, caspase-9 and p53. Tumor multiplicity was found 19.6, 5.2 in the control and ST treated groups respectively. Caspase-3, -8, -9 and p53 were significantly (P < 0.05) upregulated in ST treated group compared to Control group. Together, this study for the first time identifies the chemopreventive effects of ST in UVB-induced carcinogenesis possibly by inducing apoptosis and upregulating p53.

【 授权许可】

CC BY   
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