TY - JOUR
T1 - Sulforaphane prevents mouse skin tumorigenesis during the stage of promotion
AU - Gills, Joell J.
AU - Jeffery, Elizabeth H.
AU - Matusheski, Nathan V.
AU - Moon, Richard C.
AU - Lantvit, Daniel D.
AU - Pezzuto, John M.
N1 - Funding Information:
This research was supported by grants P01 CA48112 awarded by the National Cancer Institute and IFAFS 52101-9596 awarded by the US Department of Agriculture.
PY - 2006/5/8
Y1 - 2006/5/8
N2 - Sulforaphane (SF), a natural product from broccoli, is known to enhance detoxification of carcinogens and block initiation of chemically-induced carcinogenesis in animal models. Cell culture and xenograft studies suggest additional roles for SF, inhibiting growth of tumors, arresting the cell cycle and enhancing apoptosis. As currently reported, topical SF (1, 5 or 10 μmol/mouse) significantly inhibited 7,12-dimethylbenz(a)anthracene/12-O-tetradecanoylphorbol 13-acetate (TPA)-induced mouse skin tumorigenesis, using either an anti-promotion protocol (SF from 1 week after carcinogen until the end of the study) or a combined anti-initiation, anti-promotion protocol (SF 7 days prior to carcinogen until the end of the study). Surprisingly, no significant effect was observed in an anti-initiation protocol (SF from 7 days prior to 7 days after carcinogen). Separately, SF inhibited TPA-induced ornithine decarboxylase activity in mouse skin, an obligate step in TPA-induced promotion of carcinogenesis. These data link this molecular mechanism to SF-dependent inhibition of the promotion of tumorigenesis.
AB - Sulforaphane (SF), a natural product from broccoli, is known to enhance detoxification of carcinogens and block initiation of chemically-induced carcinogenesis in animal models. Cell culture and xenograft studies suggest additional roles for SF, inhibiting growth of tumors, arresting the cell cycle and enhancing apoptosis. As currently reported, topical SF (1, 5 or 10 μmol/mouse) significantly inhibited 7,12-dimethylbenz(a)anthracene/12-O-tetradecanoylphorbol 13-acetate (TPA)-induced mouse skin tumorigenesis, using either an anti-promotion protocol (SF from 1 week after carcinogen until the end of the study) or a combined anti-initiation, anti-promotion protocol (SF 7 days prior to carcinogen until the end of the study). Surprisingly, no significant effect was observed in an anti-initiation protocol (SF from 7 days prior to 7 days after carcinogen). Separately, SF inhibited TPA-induced ornithine decarboxylase activity in mouse skin, an obligate step in TPA-induced promotion of carcinogenesis. These data link this molecular mechanism to SF-dependent inhibition of the promotion of tumorigenesis.
KW - 12-O-Tetradecanoylphorbol 13-acetate.
KW - 7,12-Dimethylbenz(a)anthracene
KW - Isothiocyanate
KW - Ornithine decarboxylase
KW - Sulforaphane
UR - http://www.scopus.com/inward/record.url?scp=33745393451&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=33745393451&partnerID=8YFLogxK
U2 - 10.1016/j.canlet.2005.05.007
DO - 10.1016/j.canlet.2005.05.007
M3 - Article
C2 - 15993536
AN - SCOPUS:33745393451
SN - 0304-3835
VL - 236
SP - 72
EP - 79
JO - Cancer Letters
JF - Cancer Letters
IS - 1
ER -