NRF2, cancer and calorie restriction

被引:100
作者
Martin-Montalvo, A. [1 ]
Villalba, J. M. [2 ]
Navas, P. [3 ,4 ]
de Cabo, R. [1 ]
机构
[1] NIA, Aging Metab & Nutr Unit, Lab Expt Gerontol, NIH, Baltimore, MD 21224 USA
[2] Univ Cordoba, Dept Biol Celular Fisiol & Inmunol, Cordoba, Spain
[3] Univ Pablo Olavide, CSIC, Ctr Andaluz Biol Desarrollo, Seville, Spain
[4] ISCIII, Ctr Biomed Res Rare Dis CIBERER, Seville, Spain
基金
美国国家卫生研究院;
关键词
calorie restriction; carcinogenesis; NRF2; phytochemicals; ANTIOXIDANT-RESPONSE ELEMENT; TRANSCRIPTION FACTOR NRF2; GLUTATHIONE-S-TRANSFERASE; DIETARY ENERGY RESTRICTION; SKIN TUMOR PROMOTION; SMALL MAF PROTEINS; CHEMICALLY-INDUCED MAMMARY; TRANSGENIC MOUSE MODEL; CENTRAL-NERVOUS-SYSTEM; CUL3-BASED E3 LIGASE;
D O I
10.1038/onc.2010.492
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The transcription factor NF-E2-related factor (NRF2) is a key regulator of several enzymatic pathways, including cytoprotective enzymes in highly metabolic organs. In this review, we summarize the ongoing research related to NRF2 activity in cancer development, focusing on in vivo studies using NRF2 knockout (KO) mice, which have helped in defining the crucial role of NRF2 in chemoprevention. The lower cancer protection observed in NRF2 KO mice under calorie restriction (CR) suggests that most of the beneficial effects of CR on the carcinogenesis process are likely mediated by NRF2. We propose that future interventions in cancer treatment would be carried out through the activation of NRF2 in somatic cells, which will lead to a delay or prevention of the onset of some forms of human cancers, and subsequently an extension of health-and lifespan. Oncogene (2011) 30, 505-520; doi: 10.1038/onc.2010.492; published online 8 November 2010
引用
收藏
页码:505 / 520
页数:16
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