4.7 Review

Dual roles of Nrf2 in cancer

Journal

PHARMACOLOGICAL RESEARCH
Volume 58, Issue 5-6, Pages 262-270

Publisher

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.phrs.2008.09.003

Keywords

Nrf2; Keap1; ARE; Glutamate cysteine ligase; Glutathione peroxidase; Thioredoxin reductase; Peroxiredoxin; Glutathione S-transferase; NAD(P)H quinone oxidoreductase-1; Heme oxygenase; MRP

Funding

  1. NIH [ES015010]
  2. American Cancer Society [RSG-07-154-01-CNE]

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In response to oxidative stress, the transcription factor NF-E2-related factor 2 (Nrf2) controls the fate of cells through transcriptional upregulation of antioxidant response element (ARE)-bearing genes, including those encoding endogenous antioxidants, phase II detoxifying enzymes, and transporters. Expression of the Nrf2-dependent proteins is critical for ameliorating or eliminating toxicants/carcinogens to maintain cellular redox homeostasis. As a result, activation of the Nrf2 pathway, by naturally-occurring compounds or synthetic chemicals at sub-toxic doses, confers protection against subsequent toxic/carcinogenic exposure. Thus, the use of dietary compounds or synthetic chemicals to boost the Nrf2-dependent adaptive response to counteract environmental insults has emerged to be a promising strategy for cancer prevention. Interestingly, recent emerging data has revealed the dark side of Nrf2. Nrf2 and its downstream genes are overexpressed in many cancer cell lines and human cancer tissues, giving cancer cells an advantage for survival and growth. Furthermore, Nrf2 is upregulated in resistant cancer cells and is thought to be responsible for acquired chemoresistance. Therefore, it may be necessary to inhibit the Nrf2 pathway during chemotherapy. This review is primarily focused on the role of Nrf-2 in cancer, with emphasis on the recent findings indicating the cancer promoting function of Nrf2 and its role in acquired chemoresistance. (c) 2008 Elsevier Ltd. All rights reserved.

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