Morpholinopropyl isothiocyanate is a novel synthetic isothiocyanate that strongly induces the antioxidant response element-dependent Nrf 2-mediated detoxifying / antioxidant enzymes in vitro and in vivo

The inductionofNF-E2-related factor-2 (Nrf2)-mediateddetoxifying/ antioxidant enzymes is recognized as an effective strategy for cancer chemoprevention. Here, we report that 3-morpholinopropyl isothiocyanate (3MP-ITC) is an exceptionally strong chemical inducer of these enzymes. Exposure of 3MP-ITC in HepG2C8 cells not only induced endogenous Nrf2 protein but also suppressed endogenous Kelch-like ECH-associated protein 1, resulting in an increased nuclear accumulation of Nrf2. Using chemical inhibitors of protein synthesis (cycloheximide) and 26S proteosomal degradation (MG-132), we observed that the induction of Nrf2 protein by 3MP-ITC appeared to be post-translationally regulated. 3MP-ITC activated ERK1/2 and JNK1/2 and the activation of antioxidant response element (ARE) by 3MP-ITC was significantly attenuated by chemical inhibition of PKC and PI3K signaling pathways in HepG2C8 cells. Treatment with 3MP-ITC significantly depleted the intracellular level of glutathione (GSH) in HepG2C8 cells and oral administration of 3MP-ITC increased the protein expression of hepatic NAD[P]H:quinone oxidoreductase-1 and Nrf2 in Nrf2 (1/1) but not in Nrf2 (2/2) mice, whereas UDP-glucuronosyl transferase 1A1 was induced in both genotypes. Our results indicate that 3MP-ITC is a novel ITC that strongly induces Nrf2-dependent ARE-mediated detoxifying/antioxidant enzymes in vitro and in vivo via the Nrf2 signaling pathway coupled with GSH depletion and activation of multiple signaling kinase pathways, which could be potentially useful agent for cancer chemoprevention.

[1]  S. Nair,et al.  Structural Influence of Isothiocyanates on the Antioxidant Response Element (ARE)-Mediated Heme Oxygenase-1 (HO-1) Expression , 2008, Pharmaceutical Research.

[2]  A. Kong,et al.  Natural dietary anti-cancer chemopreventive compounds: redox-mediated differential signaling mechanisms in cytoprotection of normal cells versus cytotoxicity in tumor cells , 2007, Acta Pharmacologica Sinica.

[3]  Shyam Biswal,et al.  Cell survival responses to environmental stresses via the Keap1-Nrf2-ARE pathway. , 2007, Annual review of pharmacology and toxicology.

[4]  E. Ho,et al.  Dietary agents as histone deacetylase inhibitors , 2006, Molecular carcinogenesis.

[5]  R. Dashwood,et al.  Chemoprotection by sulforaphane: keep one eye beyond Keap1. , 2006, Cancer letters.

[6]  A. Kong,et al.  Nrf2: a potential molecular target for cancer chemoprevention by natural compounds. , 2006, Antioxidants & redox signaling.

[7]  A. Giudice,et al.  Activation of the Nrf2-ARE signaling pathway: a promising strategy in cancer prevention. , 2006, BioEssays : news and reviews in molecular, cellular and developmental biology.

[8]  Donna D. Zhang Mechanistic Studies of the Nrf2-Keap1 Signaling Pathway , 2006, Drug metabolism reviews.

[9]  A. Kong,et al.  Chemopreventive functions of isothiocyanates. , 2005, Drug news & perspectives.

[10]  Y. Surh,et al.  Nrf2 as a novel molecular target for chemoprevention. , 2005, Cancer letters.

[11]  A. Kong,et al.  Dietary cancer-chemopreventive compounds: from signaling and gene expression to pharmacological effects. , 2005, Trends in pharmacological sciences.

[12]  A. Kong,et al.  Differential expression and stability of endogenous nuclear factor E2-related factor 2 (Nrf2) by natural chemopreventive compounds in HepG2 human hepatoma cells. , 2005, Journal of biochemistry and molecular biology.

[13]  Yue Xiong,et al.  BTB Protein Keap1 Targets Antioxidant Transcription Factor Nrf2 for Ubiquitination by the Cullin 3-Roc1 Ligase , 2005, Molecular and Cellular Biology.

[14]  Mark Hannink,et al.  Keap1 Is a Redox-Regulated Substrate Adaptor Protein for a Cul3-Dependent Ubiquitin Ligase Complex , 2004, Molecular and Cellular Biology.

[15]  A. Kong,et al.  Chemoprevention by isothiocyanates and their underlying molecular signaling mechanisms. , 2004, Mutation research.

[16]  Yuesheng Zhang Cancer-preventive isothiocyanates: measurement of human exposure and mechanism of action. , 2004, Mutation research.

[17]  A. Agarwal,et al.  The story so far: Molecular regulation of the heme oxygenase-1 gene in renal injury. , 2004, American journal of physiology. Renal physiology.

[18]  Paul Talalay,et al.  Protection against electrophile and oxidant stress by induction of the phase 2 response: Fate of cysteines of the Keap1 sensor modified by inducers , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[19]  J. D. Engel,et al.  Keap1-null mutation leads to postnatal lethality due to constitutive Nrf2 activation , 2003, Nature Genetics.

[20]  J. Ingelfinger,et al.  Heme activates the heme oxygenase-1 gene in renal epithelial cells by stabilizing Nrf2. , 2003, American journal of physiology. Renal physiology.

[21]  H. Huang,et al.  Increased Protein Stability as a Mechanism That Enhances Nrf2-mediated Transcriptional Activation of the Antioxidant Response Element , 2003, The Journal of Biological Chemistry.

[22]  J. Alam,et al.  Degradation of Transcription Factor Nrf2 via the Ubiquitin-Proteasome Pathway and Stabilization by Cadmium* , 2003, The Journal of Biological Chemistry.

[23]  J. Lampe,et al.  Brassica, biotransformation and cancer risk: genetic polymorphisms alter the preventive effects of cruciferous vegetables. , 2002, The Journal of nutrition.

[24]  R. Cole,et al.  Direct evidence that sulfhydryl groups of Keap1 are the sensors regulating induction of phase 2 enzymes that protect against carcinogens and oxidants , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[25]  Ken Itoh,et al.  Enhanced Expression of the Transcription Factor Nrf2 by Cancer Chemopreventive Agents: Role of Antioxidant Response Element-Like Sequences in the nrf2 Promoter , 2002, Molecular and Cellular Biology.

[26]  K. Itoh,et al.  A Sulforaphane Analogue That Potently Activates the Nrf2-dependent Detoxification Pathway* , 2002, The Journal of Biological Chemistry.

[27]  M. Karin,et al.  Mammalian MAP kinase signalling cascades , 2001, Nature.

[28]  Y. Mo,et al.  Activation of Mitogen-activated Protein Kinase Pathways Induces Antioxidant Response Element-mediated Gene Expression via a Nrf2-dependent Mechanism* , 2000, The Journal of Biological Chemistry.

[29]  G. Williamson,et al.  7-Methylsulfinylheptyl and 8-methylsulfinyloctyl isothiocyanates from watercress are potent inducers of phase II enzymes. , 2000, Carcinogenesis.

[30]  J. Fahey,et al.  Antioxidant functions of sulforaphane: a potent inducer of Phase II detoxication enzymes. , 1999, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.

[31]  S. Hecht,et al.  Chemoprevention of cancer by isothiocyanates, modifiers of carcinogen metabolism. , 1999, The Journal of nutrition.

[32]  W. Wasserman,et al.  Functional antioxidant responsive elements. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[33]  U. H. Danielson,et al.  Isothiocyanates as substrates for human glutathione transferases: structure-activity studies. , 1995, The Biochemical journal.

[34]  T. Kensler,et al.  Anticarcinogenic activities of sulforaphane and structurally related synthetic norbornyl isothiocyanates. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[35]  P. Talalay,et al.  Anticarcinogenic activities of organic isothiocyanates: chemistry and mechanisms. , 1994, Cancer research.

[36]  L. Tang,et al.  Cancer-preventive isothiocyanates: dichotomous modulators of oxidative stress. , 2005, Free radical biology & medicine.

[37]  A. Kong,et al.  Differential Expression and Stability of Endogenous Nuclear Factor E 2-related Factor 2 ( Nrf 2 ) by Natural Chemopreventive Compounds in HepG 2 Human Hepatoma Cells , 2005 .