Jiang Qing-Feng, Tian Yu-Wei, Shen Quan, Xue Huan-Zhou, Li Ke
Department of Hepatobiliary Surgery, Henan Provincial People's Hospital, Zhengzhou, 450003, Henan, China.
Tumour Biol. 2014 Oct;35(10):9677-82. doi: 10.1007/s13277-014-2239-8. Epub 2014 Jun 27.
SUMOylation and deSUMOylation are dynamic mechanisms regulating a spectrum of protein activities. The SUMO proteases (SENP) remove SUMO conjugate from proteins, and their expression is deregulated in cancers. SENP2 has been reported to play a critical role in the control of hepatocellular carcinoma (HCC) cell growth by modulating the stability of β-catenin. However, the underlying mechanism remains largely unknown. Here, we show that the WW domain-containing oxidoreductase (WWOX), a novel inhibitor of the Wnt/β-catenin pathway, is required for stabilization of β-catenin regulated by SENP2 in HCC cells. The transcriptional level of WWOX is tightly regulated by SENP2. Moreover, knockdown of WWOX by siRNA attuned SENP2-induced β-catenin degradation and decreased SENP2-mediated HCC cell proliferation arrest. Taken together, our data suggested that WWOX is a key downstream modulator of the SENP2 tumor suppressor function in HCC cell.
SUMO化和去SUMO化是调节一系列蛋白质活性的动态机制。SUMO蛋白酶(SENP)从蛋白质上去除SUMO共轭物,其表达在癌症中失调。据报道,SENP2通过调节β-连环蛋白的稳定性在肝细胞癌(HCC)细胞生长控制中起关键作用。然而,其潜在机制仍 largely未知。在这里,我们表明含WW结构域的氧化还原酶(WWOX)是Wnt/β-连环蛋白途径的新型抑制剂,是HCC细胞中由SENP2调节的β-连环蛋白稳定所必需的。WWOX的转录水平受到SENP2的严格调控。此外,通过siRNA敲低WWOX可调整SENP2诱导的β-连环蛋白降解,并减少SENP2介导的HCC细胞增殖停滞。综上所述,我们的数据表明WWOX是HCC细胞中SENP2肿瘤抑制功能的关键下游调节因子。