Gene expression profiles induced by cancer chemopreventive isothiocyanate sulforaphane in the liver of C57BL/6J mice and C57BL/6J/Nrf2 (-/-) mice

被引:195
作者
Hu, Rong
Xu, Changjiang
Shen, Guoxiang
Jain, Mohit R.
Khor, Tin Oo
Gopalkrishnan, Avantika
Lin, Wen
Reddy, Bandaru
Chan, Jefferson Y.
Kong, Ah-Ng Tony
机构
[1] Rutgers State Univ, Ernest Mario Sch Pharm, Dept Pharmaceut, Piscataway, NJ 08854 USA
[2] Rutgers State Univ, Ernest Mario Sch Pharm, Grad Prog Pharmaceut Sci, Piscataway, NJ 08854 USA
[3] Rutgers State Univ, Ernest Mario Sch Pharm, Dept Biol Chem, Piscataway, NJ 08854 USA
[4] Rutgers State Univ, Ernest Mario Sch Pharm, Ctr Canc Prevent Res, Piscataway, NJ 08854 USA
[5] Univ Calif Irvine, Dept Pathol, Irvine, CA 92697 USA
关键词
SFN; antioxidant response element; Nrf2; phase II detoxifying genes; microarray; gene expression profile; knock-out mice;
D O I
10.1016/j.canlet.2005.11.050
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Sulforaphane (SFN) is a potent and promising naturally occurring dietary cancer chemopreventive compound that exerts its cancer protective effects by the induction of genes including cellular defensive genes such as phase 11 detoxifying and antioxidant enzymes. This gene induction primarily occurs via the transcription factor Nrf2 acting on the antioxidant response element (ARE) located at the 5'-flanking region of these genes. In the present study, transcriptional expression profiles of the livers obtained from the nrj2 wild-type mice and the nrj2 knockout (-/-) mice after treatments with vehicle or SFN at 3 and 12 h were generated using the Affymetrix 39 K oligonucleotide microarray. The Nrf2-dependent, SFN-inducible genes were identified which include detoxitication phase 1, 11 drug metabolizing enzymes and phase III transporters. Unexpected clusters of genes include genes for heat shock proteins (HSP), ubiquitin/26 S proteasome subunits, and lipid metabolism genes. Collectively, SFN increases the expression of genes through the Nrf2 signaling pathway that directly detoxify exogenous toxins/carcinogens or endogenous reactive oxygen species, and genes involved in the recognition and repair/removal of damaged proteins, which could provide secondary protection against DNA or protein damage that enhance cell survival. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:170 / 192
页数:23
相关论文
共 79 条
[1]   Nrf2, a Cap'n'Collar transcription factor, regulates induction of the heme oxygenase-1 gene [J].
Alam, J ;
Stewart, D ;
Touchard, C ;
Boinapally, S ;
Choi, AMK ;
Cook, JL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (37) :26071-26078
[2]   Accelerated DNA adduct formation in the lung of the Nrf2 knockout mouse exposed to diesel exhaust [J].
Aoki, Y ;
Sato, H ;
Nishimura, N ;
Takahashi, S ;
Itoh, K ;
Yamamoto, M .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2001, 173 (03) :154-160
[3]   Nrf2 transcription factor, a novel target of keratinocyte growth factor action which regulates gene expression and inflammation in the healing skin wound [J].
Braun, S ;
Hanselmann, C ;
Gassmann, MG ;
Keller, UAD ;
Born-Berclaz, C ;
Chan, KM ;
Kan, YW ;
Werner, S .
MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (15) :5492-5505
[4]   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
[5]   An important function of Nrf2 in combating oxidative stress: Detoxification of acetaminophen [J].
Chan, KM ;
Han, XD ;
Kan, YW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (08) :4611-4616
[6]   Loss of the Nrf2 transcription factor causes a marked reduction in constitutive and inducible expression of the glutathione S-transferase Gsta1, Gsta2, Gstm1, Gstm2, Gstm3 and Gstm4 genes in the livers of male and female mice [J].
Chanas, SA ;
Jiang, Q ;
McMahon, M ;
McWalter, GK ;
McLellan, LI ;
Elcombe, CR ;
Henderson, CJ ;
Wolf, CR ;
Moffat, GJ ;
Itoh, K ;
Yamamoto, M ;
Hayes, JD .
BIOCHEMICAL JOURNAL, 2002, 365 (02) :405-416
[7]   Dietary chemopreventive compounds and ARE/EpRE signaling [J].
Chen, C ;
Kong, ANT .
FREE RADICAL BIOLOGY AND MEDICINE, 2004, 36 (12) :1505-1516
[8]  
Chiao JW, 2000, INT J ONCOL, V16, P1215
[9]   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
[10]   INTAKE OF FOODS AND NUTRIENTS AND CANCER OF THE EXOCRINE PANCREAS - A POPULATION-BASED CASE-CONTROL STUDY IN THE NETHERLANDS [J].
DEMESQUITA, HBB ;
MAISONNEUVE, P ;
RUNIA, S ;
MOERMAN, CJ .
INTERNATIONAL JOURNAL OF CANCER, 1991, 48 (04) :540-549