Yu Qian, Zhou Binhua P, Wu Yadi
Pharmacology and Nutritional Sciences, the University of Kentucky, College of Medicine, Lexington, KY 40506, USA.
Markey Cancer Center, the University of Kentucky, College of Medicine, Lexington, KY 40506, USA.
Cancer Cell Microenviron. 2017;4(2). Epub 2017 Jul 3.
Metastasis accounts for a majority of cancer death. One key feature during metastasis is epithelial-mesenchymal transition (EMT), which is regulated by transcription factors such as Snail and Twist. In non-malignant cells, Snail has a short half-life and is degraded via ubiquitination, but its stability is increased in cancer cell. However, the mechanism by which Snail escapes ubiquitination and degradation remains unknown. Recently, we found that Dub3 is a deubiquinase of Snail. Most importantly, we determined that Dub3 responded to extracellular signals such as IL-6, and that the resultant signaling prevented Snail degradation, and promoted cancer growth, invasion, and migration. In this highlight, we present a concise picture of how the transcription factor Snail is regulated by ubiquitination in cancer cells, the role of Dub3 in this process, and its potential use as a treatment target.
转移是癌症死亡的主要原因。转移过程中的一个关键特征是上皮-间质转化(EMT),它受Snail和Twist等转录因子调控。在非恶性细胞中,Snail半衰期短,通过泛素化降解,但在癌细胞中其稳定性增加。然而,Snail逃避泛素化和降解的机制尚不清楚。最近,我们发现Dub3是Snail的去泛素酶。最重要的是,我们确定Dub3对IL-6等细胞外信号有反应,由此产生的信号传导可防止Snail降解,并促进癌症生长、侵袭和迁移。在本综述中,我们简要介绍了转录因子Snail在癌细胞中如何受泛素化调控、Dub3在此过程中的作用及其作为治疗靶点的潜在用途。