Sulforaphane retards the growth of human PC-3 xenografts and inhibits HDAC activity in human subjects

被引:30
作者
Myzak, Melinda C.
Tong, Philip
Dashwood, Wan-Mohaiza
Dashwood, Roderick H.
Ho, Emily
机构
[1] Oregon State Univ, Linus Pauling Inst, Corvallis, OR 97331 USA
[2] Oregon State Univ, Mol & Cellular Biol Program, Corvallis, OR 97331 USA
[3] Oregon State Univ, Dept Environm & Mol Toxicol, Corvallis, OR 97331 USA
[4] Oregon State Univ, Dept Nutr & Exercise Sci, Corvallis, OR 97331 USA
关键词
prostate cancer; histone deacetylase inhibitor; sulforaphane mechanisms of prevention; diet and cancer;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 [基础医学];
摘要
Sulforaphane (SFN) is an isothiocyanate found in cruciferous vegetables such as broccoli. This anticarcinogen was first identified as a potent inducer of Phase 2 enzymes, but evidence is mounting that SFN acts through other cancer chemopreventive mechanisms. We recently reported on a novel mechanism of chemoprotection by SFN in human colon cancer cells and prostate epithelial cells, namely the inhibition of histone deacetylase (HDAC). In the present investigation, we sought to test whether SFN also might inhibit HDAC activity in vivo. When consumed in the diet at an average daily dose of 7.5 mu mol per animal for 21 days, SFN suppressed the growth of human PC-3 prostate cancer cells by 40% in male nude mice. There was a significant decrease in HDAC activity in the xenografts, as well as in the prostates and mononuclear blood cells (MBC), of mice treated with SFN, compared to controls. There also was a trend towards increased global histone acetylation in the xenografts, prostates, and MBC. In human subjects, a single dose of 68 g BroccoSprouts inhibited HDAC activity significantly in peripheral blood mononuclear cells (PBMC) 3 and 6 hrs following consumption. These findings provide evidence that one mechanism through which SFN acts as a cancer chmopreventive agent in vivo is through the inhibition of HDAC activity. Moreover, the data suggest that HDAC activity in PBMC may be used as a biomarker for assessing exposure to novel dietary HDAC inhibitors in human subjects.
引用
收藏
页码:227 / 234
页数:8
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