FOXO transcription factors in cell-cycle regulation and the response to oxidative stress

被引:193
作者
Furukawa-Hibi, Y
Kobayashi, Y
Chen, C
Motoyama, N
机构
[1] Natl Ctr Geriatr & Gerontol, Dept Geriatr Res, Natl Inst Longev Sci, Aichi 4748522, Japan
[2] Nagoya Univ, Grad Sch Med, Dept Aging Res, Nagoya, Aichi 464, Japan
关键词
D O I
10.1089/ars.2005.7.752
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
Mammalian forkhead members of the class O (FOXO) transcription factors, including FOXO1, FOXO3a, and FOXO4, are implicated in the regulation of a variety of cellular processes, including the cell cycle, apoptosis, DNA repair, stress resistance, and metabolism. FOXO proteins are negatively regulated by the phosphatidylinositol 3-kinase-Akt signaling pathway, which is activated by growth factors and cytokines. Recent studies indicate that the activities of FOXO proteins are also regulated by oxidative stress, which induces their phosphorylation, translocation to the nucleus, and acetylation-deacetylation. Similar to the tumor suppressor p53, FOXO is activated by stress and induces the expression of genes that contribute to cell-cycle arrest, suggesting that it also functions as a tumor suppressor.
引用
收藏
页码:752 / 760
页数:9
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