Molecular Targets of Dietary Phenethyl Isothiocyanate and Sulforaphane for Cancer Chemoprevention

被引:294
作者
Cheung, Ka Lung [1 ]
Kong, Ah-Ng [1 ]
机构
[1] Rutgers State Univ, Dept Pharmaceut, Ernest Mario Sch Pharm, Grad Program Pharmaceut Sci, Piscataway, NJ 08854 USA
来源
AAPS JOURNAL | 2010年 / 12卷 / 01期
基金
美国国家卫生研究院;
关键词
dietary cancer chemoprevention; NF-kB; Nrf2; phenethyl isothiocyanate; sulforaphane; CELL-CYCLE ARREST; FACTOR-KAPPA-B; GLUTATHIONE S-TRANSFERASES; TRAIL-INDUCED APOPTOSIS; GENE-EXPRESSION; METABOLIZING-ENZYMES; SIGNALING PATHWAYS; CHEMICAL CARCINOGENESIS; OXIDATIVE STRESS; ADDUCT FORMATION;
D O I
10.1208/s12248-009-9162-8
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Development of cancer is a long-term and multistep process which comprises initiation, progression, and promotion stages of carcinogenesis. Conceivably, it can be targeted and interrupted along these different stages. In this context, many naturally occurring dietary compounds from our daily consumption of fruits and vegetables have been shown to possess cancer preventive effects. Phenethyl isothiocyanate (PEITC) and sulforaphane (SFN) are two of the most widely investigated isothiocyanates from the crucifers. Both have been found to be very potent chemopreventive agents in numerous animal carcinogenesis models as well as cell culture models. They exert their chemopreventive effects through regulation of diverse molecular mechanisms. In this review, we will discuss the molecular targets of PEITC and SFN potentially involved in cancer chemoprevention. These include the regulation of drug-metabolizing enzymes phase I cytochrome P450s and phase II metabolizing enzymes. In addition, the signaling pathways including Nrf2-Keap 1, anti-inflammatory NF kappa B, apoptosis, and cell cycle arrest as well as some receptors will also be discussed. Furthermore, we will also discuss the similarities and their potential differences in the regulation of these molecular targets by PEITC and SFN.
引用
收藏
页码:87 / 97
页数:11
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