Dietary chemopreventive compounds and ARE/EpRE signaling

被引:221
作者
Chen, C [1 ]
Kong, ANT [1 ]
机构
[1] Rutgers State Univ, Dept Pharmaceut, Ernest Mario Sch Pharm, Piscataway, NJ 08854 USA
关键词
dietary chemopreventive compounds; detoxifying enzymes; antioxidant response element; electrophile response element; nuclear factor E-2-related factor 2; Kelch-like ECH associating protein 1; mitogen-activated protein kinase; protein kinase C; phosphatidylinositol; 3-kinase; free radicals;
D O I
10.1016/j.freeradbiomed.2004.03.015
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Chemoprevention comprises multiple intervention methods using either pharmacological or dietary agents to impede, arrest, or reverse carcinogenesis at various stages. Development of dietary compounds as potential cancer chemopreventive agents is highly desirable, due to their safety, low toxicity, and general acceptance as dietary supplements. In this review, potential application of the dietary detoxifying enzyme inducers for chemoprevention and their relevant signaling events are discussed. Overall, the detoxifying enzyme system plays an important role in determining the final fate of carcinogens/procarcinogens and their subsequent impact on carcinogenesis. Among those positive regulators, phenolic and sulfur-containing compounds are two major classes of dietary detoxifying enzyme inducers. Regulation of many detoxifying enzymes by dietary chemopreventive compounds is mediated by the antioxidant response element (ARE)/electrophile response element (EpRE), which is located in the promoter region of related genes. Transcription factor nuclear factor E2-related factor 2 (Nrf2) binds to the ARE sequence to initiate gene expression. In response to treatments of various detoxifying enzyme inducers, several signal transduction pathways, including the oxidative stress, mitogen-active protein kinase, protein kinase C, and phosphatidylinositol 3-kinase pathways, are activated. The consequences of the activation of these signaling cascades, whether directly or indirectly, lead to the dissociation of Nrf2 from its cytosolic sequester Kelch-like ECH associating protein 1, nuclear translocation, and accumulation of Nrf2 protein in the nucleus, and ultimately increase the expression level of detoxifying enzymes through transcriptional activation of ARE/EpRE in those responsible genes. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:1505 / 1516
页数:12
相关论文
共 101 条
[1]
Alberts DS, 1999, CANCER RES, V59, P4743
[2]
Dietary agents in cancer prevention: flavonoids and isoflavonoids [J].
Birt, DF ;
Hendrich, S ;
Wang, WQ .
PHARMACOLOGY & THERAPEUTICS, 2001, 90 (2-3) :157-177
[3]
BLOOM DA, 2003, J BIOL CHEM, V28, P28
[4]
REGULATION OF RAS-MEDIATED SIGNALING - MORE THAN ONE-WAY TO SKIN A CAT [J].
BURGERING, BMT ;
BOS, JL .
TRENDS IN BIOCHEMICAL SCIENCES, 1995, 20 (01) :18-22
[5]
PARALLEL SIGNAL-PROCESSING AMONG MAMMALIAN MAPKS [J].
CANO, E ;
MAHADEVAN, LC .
TRENDS IN BIOCHEMICAL SCIENCES, 1995, 20 (03) :117-122
[6]
Nrf2 is essential for protection against acute pulmonary injury in mice [J].
Chan, KM ;
Kan, YW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (22) :12731-12736
[7]
NRF2, a member of the NFE2 family of transcription factors, is not essential for murine erythropoiesis, growth, and development [J].
Chan, KM ;
Lu, RH ;
Chang, JC ;
Kan, YW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (24) :13943-13948
[8]
MEKK3 directly regulates MEK5 activity as part of the big mitogen-activated protein kinase 1 (BMK1) signaling pathway [J].
Chao, TH ;
Hayashi, M ;
Tapping, RI ;
Kato, Y ;
Lee, JD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (51) :36035-36038
[9]
Activation of antioxidant-response element (ARE), mitogen-activated protein kinases (MAPKs) and caspases by major green tea polyphenol components during cell survival and death [J].
Chen, C ;
Yu, R ;
Owuor, ED ;
Kong, ANT .
ARCHIVES OF PHARMACAL RESEARCH, 2000, 23 (06) :605-612
[10]
Chemoprevention of colonic aberrant crypt foci in Fischer rats by sulforaphane and phenethyl isothiocyanate [J].
Chung, FL ;
Conaway, CC ;
Rao, CV ;
Reddy, BS .
CARCINOGENESIS, 2000, 21 (12) :2287-2291