Activation of coupled Ah receptor and Nrf2 gene batteries by dietary phytochemicals in relation to chemoprevention

被引:106
作者
Koehle, Christoph [1 ]
Bock, Karl Walter [1 ]
机构
[1] Univ Tubingen, Inst Pharmacol & Toxicol, Dept Toxicol, D-72074 Tubingen, Germany
关键词
Ah receptor; Nrf2; phytochemicals; mixed Ah receptor/Nrf2 activators; chemoprevention;
D O I
10.1016/j.bcp.2006.04.017
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The Ah receptor (AhR) is a ligand-activated transcription factor and member of the bHLH/PAS (basic helix-loop-helix/Per-Arnt-Sim) family of chemosensors and developmental regulators. it represents a multifunctional molecular switch involved in regulation of endo- and xenobiotic metabolism, in vascular development and in dioxin-mediated toxicities. Recently, the oxidative stress-protecting Nrf2 has been shown to be a downstream target of the AhR [Miao W, Hu L, Scrivens PJ, Batist G. Transcriptional regulation of NF-E2 p45-regulated factor (NRF2) expression by the aryl hydrocarbon receptor-xenobiotic response element signaling pathway. J Biol Chem 2005;280:20340-8). This finding offers the possibility that distinct but partially overlapping AhR and Nrf2 gene batteries of Phase 11 xenobiotic-metabolizing enzymes can be synergistically activated by a number of phytochemicals, acting as selective or mixed activators of target genes. In addition, it is conceivable that AhR-mediated oxidative/electrophile stress may be attenuated by coupled Nrf2 activation. The commentary discusses potentials and limitations of (i) selective Nrf2 and of (ii) synergistic AhR plus Nrf2 activation by phytochemicals in efforts towards chemoprevention of cancer and degenerative diseases, and describes clinical trials providing the expectation that chemopreventive measures may favorably modulate unavoidable endo- and exogenous toxin exposures in high risk populations. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:795 / 805
页数:11
相关论文
共 82 条
[11]   UDP-glucuronosyltransferase 1A6:: Structural, functional, and regulatory aspects [J].
Bock, KW ;
Köhle, C .
PHASE II CONJUGATION ENZYMES AND TRANSPORT SYSTEMS, 2005, 400 :57-75
[12]  
BOCK KW, IN PRESS BIOCH PHARM
[13]   Influence of t-butylhydroquinone and β-naphthoflavone on formation and transport of 4-methylumbelliferone glucuronide in Caco-2/TC-7 cell monolayers [J].
Bock-Hennig, BS ;
Köhle, C ;
Nill, KC ;
Bock, KW .
BIOCHEMICAL PHARMACOLOGY, 2002, 63 (02) :123-128
[14]  
Bonnesen C, 2001, CANCER RES, V61, P6120
[15]   Aryl hydrocarbon receptor-mediated antiestrogenic and antitumorigenic activity of diindolylmethane [J].
Chen, I ;
McDougal, A ;
Wang, F ;
Safe, S .
CARCINOGENESIS, 1998, 19 (09) :1631-1639
[16]   Tissue-specific, inducible, and hormonal control of the human UDP-glucuronosyltransferase-1 (UGT1) locus [J].
Chen, SJ ;
Beaton, D ;
Nguyen, N ;
Senekeo-Effenberger, K ;
Brace-Sinnokrak, E ;
Argikar, U ;
Remmel, RP ;
Trottier, J ;
Barbier, O ;
Ritter, JK ;
Tukey, RH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (45) :37547-37557
[17]   4-Hydroxynonenal induces adaptive response and enhances PC12 cell tolerance primarily through induction of thioredoxin reductase 1 via activation of Nrf2 [J].
Chen, ZH ;
Saito, Y ;
Yoshida, Y ;
Sekine, A ;
Noguchi, N ;
Niki, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (51) :41921-41927
[18]   Disruption of cell-cell contact maximally but transiently activates AhR-mediated transcription in 10T1/2 fibroblasts [J].
Cho, YC ;
Zheng, WC ;
Jefcoate, CR .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2004, 199 (03) :220-238
[19]  
Conney AH, 2003, CANCER RES, V63, P7005
[20]  
CONNEY AH, 1982, CANCER RES, V42, P4875