Activation of Nrf2-antioxidant signaling attenuates NFκB-inflammatory response and elicits apoptosis

Wenge Li, Tin Oo Khor, Changjiang Xu, Guoxiang Shen, Woo Sik Jeong, Siwang Yu, Ah Ng Kong

Research output: Contribution to journalArticle

445 Scopus citations

Abstract

Oxidative stress has been implicated in the etiology of neurodegenerative disease, cancer and aging. Indeed, accumulation of reactive oxygen and nitrogen species generated by inflammatory cells that created oxidative stress is thought to be one of the major factor by which chronic inflammation contributes to neoplastic transformation as well as many other diseases. We have recently reported that mice lacking nuclear factor-erythroid 2-related factor 2 (Nrf2) are more susceptible to dextran sulfate sodium (DSS)-induced colitis and colorectal carcinogenesis. Nrf2 is a basic leucine zipper redox-sensitive transcriptional factor that plays a center role in ARE (antioxidant response element)-mediated induction of phase II detoxifying and antioxidant enzymes. We found that increased susceptibility of Nrf2 deficient mice to DSS-induced colitis and colorectal cancer was associated with decreased expression of antioxidant/phase II detoxifying enzymes in parallel with upregulation of pro-inflammatory cytokines/biomarkers. These findings suggest that Nrf2 may play an important role in defense against oxidative stress possibly by activation of cellular antioxidant machinery as well as suppression of pro-inflammatory signaling pathways. In addition, in vivo and in vitro data generated from our laboratory suggest that many dietary compounds can differentially regulate Nrf2-mediated antioxidant/anti-inflammatory signaling pathways as the first line defense or induce apoptosis once the cells have been damaged. In this review, we will summarize our thoughts on the potential cross-talks between Nrf2 and NFκB pathways. Although the mechanisms involved in the cross-talk between these signaling pathways are still illusive, targeting Nrf2-antioxidative stress signaling is an ideal strategy to prevent or treat oxidative stress-related diseases.

Original languageEnglish (US)
Pages (from-to)1485-1489
Number of pages5
JournalBiochemical Pharmacology
Volume76
Issue number11
DOIs
StatePublished - Dec 1 2008
Externally publishedYes

Keywords

  • AOM
  • Apoptosis
  • DSS
  • NFκB
  • Nrf2

ASJC Scopus subject areas

  • Biochemistry
  • Pharmacology

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