FOXO1: A Potential Target for Human Diseases

被引:86
作者
Lu, Huarui [2 ]
Huang, Haojie [1 ,2 ,3 ]
机构
[1] SUNY Stony Brook, Dept Pathol, Med Ctr, Stony Brook, NY 11794 USA
[2] Univ Minnesota, Masonic Canc Ctr, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Dept Lab Med & Pathol, Minneapolis, MN 55455 USA
基金
美国国家卫生研究院;
关键词
FoxO transcription factors; posttranslational modification; apoptosis; the cell cycle; glucose metabolism; cancer; diabetes; muscle atrophy; FORKHEAD TRANSCRIPTION FACTOR; PROTEIN-KINASE-B; PROSTATE-CANCER CELLS; FACTOR FKHR; ANDROGEN RECEPTOR; LIFE-SPAN; NUCLEAR EXCLUSION; SKELETAL-MUSCLE; FAMILY-MEMBER; DNA-BINDING;
D O I
10.2174/138945011796150280
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The forkhead box O (FoxO) transcription factors are known to be involved in many physiological and pathological processes including apoptosis, cell cycle arrest, stress resistance, glucose metabolism, cellular differentiation and development, and tumor suppression. The environmental cues, such as growth factors, nutrients, oxidative stress and irradiation, can either positively or negatively modulate FoxO proteins' activities, thereby ensuring distinctive transcription programs in the cell. The potent activities of FoxOs are tightly controlled by multiple mechanisms, which include posttranslational modification such as phosphorylation, acetylation, methylation and ubiquitination, subcellular localization, and direct protein-protein interaction. Mounting evidence suggests that the human FOXO1 protein, a founding member of the FoxO family is likely involved in carcinogenesis, diabetes and other human diseases. Here we give an overview of most recent findings regarding the regulation and function of FoxO1, its potential role in human diseases and useful animal models for functional studies on FoxO1. Prospective ways in which the discoveries from the basic research of FoxO1 can be utilized for drug targeting and development of novel therapeutics for human diseases are also discussed.
引用
收藏
页码:1235 / 1244
页数:10
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