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萝卜硫素可延缓人PC-3异种移植瘤的生长,并抑制人体中的组蛋白去乙酰化酶活性。

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

作者信息

Myzak Melinda C, Tong Philip, Dashwood Wan-Mohaiza, Dashwood Roderick H, Ho Emily

机构信息

Linus Pauling Institute, Molecular and Cellular Biology Program, Oregon State University, Corvallis, Oregon 97331, USA.

出版信息

Exp Biol Med (Maywood). 2007 Feb;232(2):227-34.

Abstract

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 mumol 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 chemopreventive 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.

摘要

萝卜硫素(SFN)是一种在西兰花等十字花科蔬菜中发现的异硫氰酸盐。这种抗癌剂最初被确定为一种强效的Ⅱ相酶诱导剂,但越来越多的证据表明,SFN通过其他癌症化学预防机制发挥作用。我们最近报道了SFN在人结肠癌细胞和前列腺上皮细胞中化学保护的一种新机制,即抑制组蛋白脱乙酰酶(HDAC)。在本研究中,我们试图测试SFN在体内是否也可能抑制HDAC活性。当以每只动物每天平均剂量7.5 μmol的量添加到饮食中,持续21天时,SFN可使雄性裸鼠体内人PC-3前列腺癌细胞的生长抑制40%。与对照组相比,接受SFN治疗的小鼠的异种移植瘤、前列腺和单核血细胞(MBC)中的HDAC活性显著降低。在异种移植瘤、前列腺和MBC中,整体组蛋白乙酰化也有增加的趋势。在人类受试者中,单次服用68 g发芽西兰花在食用后3小时和6小时可显著抑制外周血单核细胞(PBMC)中的HDAC活性。这些发现提供了证据,表明SFN在体内作为癌症化学预防剂发挥作用的一种机制是通过抑制HDAC活性。此外,数据表明PBMC中的HDAC活性可用作评估人类受试者接触新型饮食HDAC抑制剂的生物标志物。

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