Department of Surgery, Shanghai Key Laboratory of Gastric Neoplasms, Shanghai Institute of Digestive Surgery, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, PR China.
Department of Surgery, Shanghai Key Laboratory of Gastric Neoplasms, Shanghai Institute of Digestive Surgery, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, PR China.
Cancer Lett. 2017 Nov 1;408:10-21. doi: 10.1016/j.canlet.2017.08.013. Epub 2017 Aug 23.
Increasing evidence demonstrates that long noncoding RNAs (lncRNAs) regulate gene and protein expression by exerting an influence on transcriptional and post-transcriptional processes. Here, we report that the lncRNA UCA1 increases the metastatic ability of gastric cancer (GC) cells by regulating GRK2 protein stability by promoting Cbl-c-mediated GRK2 ubiquitination and degradation. This process then activates the ERK-MMP9 signalling pathway. Furthermore, we demonstrate that GRK2 is downregulated in GC cells and that silencing of GRK2 might cause similar phenotypic changes and signalling pathway activation as those induced by elevated UCA1 in GC cells. Our results suggest that UCA1 might function as a mediator of protein ubiquitination and may be a promising molecular target for GC therapy.
越来越多的证据表明,长链非编码 RNA(lncRNA)通过影响转录和转录后过程来调节基因和蛋白质的表达。在这里,我们报告说 lncRNA UCA1 通过促进 Cbl-c 介导的 GRK2 泛素化和降解来调节 GRK2 蛋白稳定性,从而增加胃癌(GC)细胞的转移能力。这一过程随后激活了 ERK-MMP9 信号通路。此外,我们证明 GRK2 在 GC 细胞中下调,沉默 GRK2 可能会导致与 GC 细胞中 UCA1 升高诱导的类似表型变化和信号通路激活。我们的研究结果表明,UCA1 可能作为蛋白质泛素化的介质发挥作用,可能是 GC 治疗的有前途的分子靶点。