4.7 Article

Identification of Nrf2-regulated genes induced by chemopreventive isothiocyanate PEITC by oligonucleotide microarray

Journal

LIFE SCIENCES
Volume 79, Issue 20, Pages 1944-1955

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.lfs.2006.06.019

Keywords

PEITC; antioxidant response element; Nrf2; phase II detoxifying genes; microarray; gene expression profile; real-time PCR

Funding

  1. NCI NIH HHS [R01-CA094828, R01-CA-073674] Funding Source: Medline

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Electrophiles generated during metabolic activation of carcinogens and reactive oxygen species formed from endogenous and exogenous sources might play a significant role in carcinogenesis. Cancer chemoprevention by induction of phase II detoxifying enzymes to counteract the insults of these reactive intermediates is under intensive investigation. Nrf2, a bZIP transcription factor, plays a central role in the regulation of phase II genes by binding to the antioxidant response element (ARE) in their promoters. Identification of novel Nrf2-regulated genes is likely to provide insight into cellular defense systems against the toxicities of electrophiles and oxidants and may define effective targets for achieving cancer chernoprevention. Phenethyl isothiocyanate (PEITC) is a promising chemopreventive agent that exerts its effects by induction of phase II enzymes via activation of Nrf2. In the present study, a transcriptional profile of liver of the wild-type(Nrf 2+/+) and knock-out (Nrf 2-/-) mice after treatments with vehicle or PEITC at 3 h and at 12 h was generated using the Affymetrix. Mouse Genome 430 2.0 Array. Comparative analysis of gene expression changes between different treatment groups of wild-type and Nrf 2-deficient mice facilitated identification of numerous genes regulated by Nrf 2. These Nrf 2-dependent and PEITC-inducible genes include known detoxication enzymes, as well as novel xenobiotic-metabolizing genes regulated by Nrf 2 such as CYP 2c55, CYP 2u1 and aldehyde oxidase. Unexpected clusters included genes for heat shock proteins, ubiquitin/26 S proteasome subunits, and lipid metabolism molecules. Collectively, the identification of these genes not only provides novel insight into the effect of PEITC on global gene expression and chemoprevention, but also reveals the role of Nrf 2 in those processes, which would confer cancer chemopreventive future. (c) 2006 Elsevier Inc. All rights reserved.

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