Forkhead Homeobox Type O Transcription Factors in the Responses to Oxidative Stress

被引:286
作者
Storz, Peter [1 ]
机构
[1] Mayo Clin, Dept Canc Biol, Jacksonville, FL 32224 USA
关键词
PANCREATIC BETA-CELLS; REGULATES LIFE-SPAN; CANCER STEM-CELLS; PROTEIN-KINASE-D; CAENORHABDITIS-ELEGANS; GENE-EXPRESSION; FACTOR FOXO1; SUPEROXIDE-DISMUTASE; SIRT1; DEACETYLASE; SIGNALING PATHWAY;
D O I
10.1089/ars.2010.3405
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
Reactive oxygen species (ROS) and cellular oxidative stress are involved in many physiological and pathophysiological processes, including cellular and organismal aging, migration, proliferation, senescence or death of normal and cancer cells, and stress resistance of stem cells. The forkhead homeobox type O (FOXO) transcription factors FOXO1, FOXO3a, and FOXO4 are critical mediators of the cellular responses to oxidative stress and have been implicated in many of the above ROS-regulated processes. In cancer cells they converge oxidative stress signaling to cell cycle arrest and cell death or promote a motile phenotype. Dependent on their posttranslational modifications FOXOs can also actively regulate the detoxification of cells from ROS and promote stress resistance. Thus, FOXO transcription factors are of vital importance in processes regulating tumor survival or progression, stem cell maintenance, age-related pathological processes, and lifespan extension. Antioxid. Redox Signal. 14, 593-605.
引用
收藏
页码:593 / 605
页数:13
相关论文
共 142 条
[1]   Sirt1 regulates aging and resistance to oxidative stress in the heart [J].
Alcendor, Ralph R. ;
Gao, Shumin ;
Zhai, Peiyong ;
Zablocki, Daniela ;
Holle, Eric ;
Yu, Xianzhong ;
Tian, Bin ;
Wagner, Thomas ;
Vatner, Stephen F. ;
Sadoshima, Junichi .
CIRCULATION RESEARCH, 2007, 100 (10) :1512-1521
[2]   Increased Lipid Oxidation Causes Oxidative Stress, Increased Peroxisome Proliferator-activated Receptor-γ Expression, and Diminished Pro-osteogenic Wnt Signaling in the Skeleton [J].
Almeida, Maria ;
Ambrogini, Elena ;
Han, Li ;
Manolagas, Stavros C. ;
Jilka, Robert L. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (40) :27438-27448
[3]   FoxO-Mediated Defense against Oxidative Stress in Osteloblasts, Is Indispensable for Skeletal Homeostasis in Mice [J].
Ambrogini, Elena ;
Almeida, Maria ;
Martin-Milian, Marta ;
Paik, Ji-Hye ;
DePinho, Ronald A. ;
Han, Li ;
Goellner, Joseph ;
Weinstein, Robert S. ;
Jilka, Robert L. ;
O'Brien, Charles A. ;
Manolagas, Stavros C. .
CELL METABOLISM, 2010, 11 (02) :136-146
[4]   Physiological functions of thioredoxin and thioredoxin reductase [J].
Arnér, ESJ ;
Holmgren, A .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2000, 267 (20) :6102-6109
[5]   NADPH oxidase: An update [J].
Babior, BM .
BLOOD, 1999, 93 (05) :1464-1476
[6]   FOXO3a is activated in response to hypoxic stress and inhibits HiF1-induced apoptosis via regulation of CITED2 [J].
Bakker, Walbert J. ;
Harris, Isaac S. ;
Mak, Tak W. .
MOLECULAR CELL, 2007, 28 (06) :941-953
[7]   Glioma stem cells promote radioresistance by preferential activation of the DNA damage response [J].
Bao, Shideng ;
Wu, Qiulian ;
McLendon, Roger E. ;
Hao, Yueling ;
Shi, Qing ;
Hjelmeland, Anita B. ;
Dewhirst, Mark W. ;
Bigner, Darell D. ;
Rich, Jeremy N. .
NATURE, 2006, 444 (7120) :756-760
[8]   Differential regulation of endogenous glucose-6-phosphatase and phosphoenolpyruvate carboxykinase gene expression by the forkhead transcription factor FKHR in H4IIE-hepatoma cells [J].
Barthel, A ;
Schmoll, D ;
Krüger, KD ;
Bahrenberg, G ;
Walther, R ;
Roth, RA ;
Joost, HG .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 285 (04) :897-902
[9]  
BENDAYAN M, 1982, LAB INVEST, V47, P364
[10]   p66Shc-generated Oxidative Signal Promotes Fat Accumulation [J].
Berniakovich, Ina ;
Trinei, Mirella ;
Stendardo, Massimo ;
Migliaccio, Enrica ;
Minucci, Saverio ;
Bernardi, Paolo ;
Pelicci, Pier Giuseppe ;
Giorgio, Marco .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (49) :34283-34293