Nrf2-Mediated Metabolic Reprogramming in Cancer

被引:53
作者
Wang, Yan-Yang [1 ,2 ]
Chen, Juan [3 ]
Liu, Xiao-Ming [4 ]
Zhao, Ren [1 ,2 ]
Zhe, Hong [1 ,2 ]
机构
[1] Ningxia Med Univ, Dept Radiat Oncol, Gen Hosp, Ningxia 750004, Peoples R China
[2] Ningxia Med Univ, Canc Inst, Ningxia 750004, Peoples R China
[3] Ningxia Med Univ, Dept Pulm & Crit Care Med, Gen Hosp, Ningxia 750004, Peoples R China
[4] Ningxia Med Univ, Human Stem Cell Inst, Gen Hosp, Ningxia 750004, Peoples R China
基金
中国国家自然科学基金;
关键词
TRANSCRIPTION FACTOR NRF2; PROTEIN-KINASE-C; KEAP1-NRF2; PATHWAY; AUTOPHAGY; CELLS; PHOSPHORYLATION; ACTIVATION; P62; GLUCOSE-6-PHOSPHATE-DEHYDROGENASE; DEGRADATION;
D O I
10.1155/2018/9304091
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Metabolic reprogramming is one of the hallmarks of cancer. Nrf2 pathway is one of the critical signaling cascades involved in cell defense and survival against oxidative stress. The significance of Nrf2 in cancer metabolism begins to be recognized. In this minireview, we focus on the Nrf2-mediated cancer metabolic reprogramming and intend to highlight the role of Nrf2 in the regulation of malignant transformation, cancer proliferation, and the development of treatment resistance via metabolic adaptations. We hope for the development of noninvasive biomarkers and novel therapeutic approaches for cancer based on Nrf2-directed cancer metabolic reprogramming in the near future.
引用
收藏
页数:7
相关论文
共 64 条
[1]   Sestrins Activate Nrf2 by Promoting p62-Dependent Autophagic Degradation of Keap1 and Prevent Oxidative Liver Damage [J].
Bae, Soo Han ;
Sung, Su Haeng ;
Oh, Sue Young ;
Lim, Jung Mi ;
Lee, Se Kyoung ;
Park, Young Nyun ;
Lee, Hye Eun ;
Kang, Dongmin ;
Rhee, Sue Goo .
CELL METABOLISM, 2013, 17 (01) :73-84
[2]   The cytoprotective role of the Keap1-Nrf2 pathway [J].
Baird, Liam ;
Dinkova-Kostova, Albena T. .
ARCHIVES OF TOXICOLOGY, 2011, 85 (04) :241-272
[3]   New aspects of the Warburg effect in cancer cell biology [J].
Bensinger, Steven J. ;
Christofk, Heather R. .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2012, 23 (04) :352-361
[4]   Phosphorylation of Nrf2 at Ser40 by protein kinase C in response to antioxidants leads to the release of Nrf2 from INrf2, but is not required for Nrf2 stabilization/accumulation in the nucleus and transcriptional activation of antioxidant response element-mediated NAD(P)H:quinone oxidoreductase-1 gene expression [J].
Bloom, DA ;
Jaiswal, AK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (45) :44675-44682
[5]  
BOKUN R, 1987, ACTA CYTOL, V31, P249
[6]   Metabolic pathways promoting cancer cell survival and growth [J].
Boroughs, Lindsey K. ;
DeBerardinis, Ralph J. .
NATURE CELL BIOLOGY, 2015, 17 (04) :351-359
[7]   Keap1/Nrf2 pathway in the frontiers of cancer and non-cancer cell metabolism [J].
Chartoumpekis, Dionysios V. ;
Wakabayashi, Nobunao ;
Kensler, Thomas W. .
BIOCHEMICAL SOCIETY TRANSACTIONS, 2015, 43 :639-644
[8]   The role of reactive oxygen species and metabolism on cancer cells and their microenvironment [J].
Costa, Ana ;
Scholer-Dahirel, Alix ;
Mechta-Grigoriou, Fatima .
SEMINARS IN CANCER BIOLOGY, 2014, 25 :23-32
[9]   Metabolic reprogramming in cancer: Unraveling the role of glutamine in tumorigenesis [J].
Daye, Dania ;
Wellen, Kathryn E. .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2012, 23 (04) :362-369
[10]   Direct evidence that sulfhydryl groups of Keap1 are the sensors regulating induction of phase 2 enzymes that protect against carcinogens and oxidants [J].
Dinkova-Kostova, AT ;
Holtzclaw, WD ;
Cole, RN ;
Itoh, K ;
Wakabayashi, N ;
Katoh, Y ;
Yamamoto, M ;
Talalay, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (18) :11908-11913