FoxO1: a novel insight into its molecular mechanisms in the regulation of skeletal muscle differentiation and fiber type specification

被引:87
|
作者
Xu, Meng [1 ]
Chen, Xiaoling [1 ]
Chen, Daiwen [1 ]
Yu, Bing [1 ]
Huang, Zhiqing [1 ]
机构
[1] Sichuan Agr Univ, Inst Anim Nutr, Key Lab Anim Dis Resistance Nutr, China Minist Educ, Chengdu, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
FoxO1; skeletal muscle; differentiation; fiber type specification; molecular mechanisms; TRANSCRIPTION FACTOR FKHR; FORKHEAD BOX-O; MYOBLAST DIFFERENTIATION; GENE-EXPRESSION; MAMMALIAN TARGET; ALVEOLAR RHABDOMYOSARCOMA; MYOGENIC DIFFERENTIATION; SIGNALING PATHWAYS; UBIQUITIN LIGASES; NUCLEAR EXCLUSION;
D O I
10.18632/oncotarget.12891
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
FoxO1, a member of the forkhead transcription factor forkhead box protein O (FoxO) family, is predominantly expressed in most muscle types. FoxO1 is a key regulator of muscle growth, metabolism, cell proliferation and differentiation. In the past two decades, many researches have indicated that FoxO1 is a negative regulator of skeletal muscle differentiation while contrasting opinions consider that FoxO1 is crucial for myoblast fusion. FoxO1 is expressed much higher in fast twitch fiber enriched muscles than in slow muscles and is also closely related to muscle fiber type specification. In this review, we summarize the molecular mechanisms of FoxO1 in the regulation of skeletal muscle differentiation and fiber type specification.
引用
收藏
页码:10662 / 10674
页数:13
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