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Redox control of cell proliferation
被引:145
|作者:
Chiu, Joyce
[1
]
Dawes, Ian W.
[1
,2
]
机构:
[1] Univ New S Wales, Sch Biotechnol & Biomol Sci, Sydney, NSW 2052, Australia
[2] Univ New S Wales, Ramaciotti Ctr Gene Funct Anal, Sydney, NSW 2052, Australia
关键词:
cell-cycle;
oxidative stress;
redox signaling;
thiol oxidation;
glutathionylation;
disulfide bond;
TYROSINE-PHOSPHATASE;
1B;
NF-KAPPA-B;
CYSTEINE-SULFINIC ACID;
JUN DNA-BINDING;
SACCHAROMYCES-CEREVISIAE;
S-GLUTATHIONYLATION;
TRANSCRIPTION FACTORS;
SIGNAL-TRANSDUCTION;
CYCLE TRANSCRIPTION;
OXIDATIVE STRESS;
D O I:
10.1016/j.tcb.2012.08.002
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Cell proliferation is regulated by multiple signaling pathways and stress surveillance systems to ensure cell division takes place with fidelity. In response to oxidative stress, cells arrest in the cell-cycle and aberrant redox control of proliferation underlies the pathogenesis of many diseases including cancer and neurodegenerative disorders. Redox sensing of cell-cycle regulation has recently been shown to involve reactive cysteine thiols that function as redox sensors in cell-cycle regulators, By modulating cell-cycle regulators these redox-active thiols ensure cell division is executed at the right redox environment. This review summarizes recent findings. on regulation of cell division by the oxidation of cysteines in cell division regulators and the potential of targeting these critical cysteine residues for cancer therapy.
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页码:592 / 601
页数:10
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