A redox cycle within the cell cycle: ring in the old with the new

被引:218
作者
Menon, S. G. [1 ]
Goswami, P. C. [1 ]
机构
[1] Univ Iowa, Dept Radiat Oncol, Free Rad & Radiat Biol Program, Med Labs, Iowa City, IA 52242 USA
关键词
redox; antioxidant enzymes; cell cycle; cyclin D1; MnSOD;
D O I
10.1038/sj.onc.1209895
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
In recent years, the intracellular oxidation-reduction ( redox) state has gained increasing attention as a critical mediator of cell signaling, gene expression changes and proliferation. This review discusses the evidence for a redox cycle ( i. e., fluctuation in the cellular redox state) regulating the cell cycle. The presence of redox-sensitive motifs ( cysteine residues, metal co-factors in kinases and phosphatases) in several cell cycle regulatory proteins indicate periodic oscillations in intracellular redox state could play a central role in regulating progression from G(0)/G(1) to S to G(2) and M cell cycle phases. Fluctuations in the intracellular redox state during cell cycle progression could represent a fundamental mechanism linking oxidative metabolic processes to cell cycle regulatory processes. Proliferative disorders are central to a variety of human pathophysiological conditions thought to involve oxidative stress. Therefore, a more complete understanding of redox control of the cell cycle could provide a biochemical rationale for manipulating aberrant cell proliferation.
引用
收藏
页码:1101 / 1109
页数:9
相关论文
共 99 条
[81]   Manganese superoxide dismutase protects the proliferative capacity of confluent normal human fibroblasts [J].
Sarsour, EH ;
Agarwal, M ;
Pandita, TK ;
Oberley, LW ;
Goswami, PC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (18) :18033-18041
[82]   Redox regulation of Cdc25C [J].
Savitsky, PA ;
Finkel, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (23) :20535-20540
[83]   Redox environment of the cell as viewed through the redox state of the glutathione disulfide/glutathione couple [J].
Schafer, FQ ;
Buettner, GR .
FREE RADICAL BIOLOGY AND MEDICINE, 2001, 30 (11) :1191-1212
[84]   Mammalian peroxisomes and reactive oxygen species [J].
Schrader, M ;
Fahimi, HD .
HISTOCHEMISTRY AND CELL BIOLOGY, 2004, 122 (04) :383-393
[85]   CDC25M2 ACTIVATION OF CYCLIN-DEPENDENT KINASES BY DEPHOSPHORYLATION OF THREONINE-14 AND TYROSINE-15 [J].
SEBASTIAN, B ;
KAKIZUKA, A ;
HUNTER, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (08) :3521-3524
[86]  
SHERR CJ, 1995, P ASSOC AM PHYSICIAN, V107, P181
[87]   STIMULATION BY XANTHINE-OXIDASE OF 3T3 SWISS FIBROBLASTS AND HUMAN-LYMPHOCYTES [J].
STIRPE, F ;
HIGGINS, T ;
TAZZARI, PL ;
ROZENGURT, E .
EXPERIMENTAL CELL RESEARCH, 1991, 192 (02) :635-638
[88]   REQUIREMENT FOR GENERATION OF H2O2 FOR PLATELET-DERIVED GROWTH-FACTOR SIGNAL-TRANSDUCTION [J].
SUNDARESAN, M ;
YU, ZX ;
FERRANS, VJ ;
IRANI, K ;
FINKEL, T .
SCIENCE, 1995, 270 (5234) :296-299
[89]   Transcriptional activation of the human glutathione peroxidase promoter by p53 [J].
Tan, MJ ;
Li, SJ ;
Swaroop, MJ ;
Guan, KL ;
Oberley, LW ;
Sun, Y .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (17) :12061-12066
[90]   E2F1 and c-Myc potentiate apoptosis through inhibition of NF-κB activity that facilitates MnSOD-mediated ROS elimination [J].
Tanaka, H ;
Matsumura, I ;
Ezoe, S ;
Satoh, Y ;
Sakamaki, T ;
Albanese, C ;
Machii, T ;
Pestell, RG ;
Kanakura, Y .
MOLECULAR CELL, 2002, 9 (05) :1017-1029