Ski and SnoN, potent negative regulators of TGF-β signaling

被引:208
作者
Deheuninck, Julien [1 ]
Luo, Kunxin [1 ]
机构
[1] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
关键词
SnoN; Ski; Signal transduction; development; tumorigenesis; TGF-beta signaling; senescence; GROWTH-FACTOR-BETA; SQUAMOUS-CELL CARCINOMA; ANAPHASE-PROMOTING COMPLEX; UBIQUITIN-DEPENDENT DEGRADATION; HISTONE DEACETYLASE COMPLEX; 1P36 DELETION SYNDROME; PROTOONCOGENE C-SKI; SMAD PROTEINS; TRANSCRIPTIONAL REPRESSION; SKELETAL-MUSCLE;
D O I
10.1038/cr.2008.324
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Ski and the closely related SnoN were discovered as oncogenes by their ability to transform chicken embryo fibroblasts upon overexpression. While elevated expressions of Ski and SnoN have also been reported in many human cancer cells and tissues, consistent with their pro-oncogenic activity, emerging evidence also suggests a potential anti-oncogenic activity for both. In addition, Ski and SnoN have been implicated in regulation of cell differentiation, especially in the muscle and neuronal lineages. Multiple cellular partners of Ski and SnoN have been identified in an effort to understand the molecular mechanisms underlying the complex roles of Ski and SnoN. In this review, we summarize recent findings on the biological functions of Ski and SnoN, their mechanisms of action and how their levels of expression are regulated.
引用
收藏
页码:47 / 57
页数:11
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