STAM-binding protein regulates melanoma metastasis through SLUG stabilization

被引:18
作者
Iwakami, Yusuke [1 ]
Yokoyama, Satoru [1 ]
Watanabe, Kensuke [1 ]
Hayakawa, Yoshihiro [1 ]
机构
[1] Univ Toyama, Inst Nat Med, Div Pathogen Biochem, 2630 Sugitani, Toyama 9300194, Japan
关键词
STAMBP; Melanoma; Metastasis; SLUG; MESENCHYMAL TRANSITION; AMSH; DEGRADATION;
D O I
10.1016/j.bbrc.2018.11.068
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
STAM-binding protein, STAMBP, is a JAMM-family deubiquitinating enzyme containing the microtubule-interacting/transport domain and STAM-binding domain. Although the biological importance of STAMBP in development has been recognized because the microcephaly-capillary malformation syndrome in human is caused by its somatic mutations, the role of STAMBP in cancer has not yet been determined. In this study, we demonstrate that STAMBP is a key molecule for regulating melanoma migration and invasion, but not survival, by knocking down STAMBP in vitro. STAMBP regulates SLUG expression through a post-transcriptional mechanism to control protein stability and further contributes to the in vivo metastatic potential of melanoma. Collectively, these results indicate the importance of STAMBP in melanoma metastasis by regulating SLUG. It is therefore a potential therapeutic target. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:484 / 488
页数:5
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