Xiong Haojun, Li Bo, He Jintao, Zeng Yijun, Zhang Yan, He Fengtian
Department of Biochemistry and Molecular Biology, College of Basic Medical Sciences, Third Military Medical University, Chongqing 400038, China.
Battalion 17 of Students, College of Preventive Medicine, Third Military Medical University, Chongqing 400038, China.
Biochem Biophys Res Commun. 2017 Aug 26;490(3):693-699. doi: 10.1016/j.bbrc.2017.06.103. Epub 2017 Jun 17.
Highly upregulated in liver cancer (HULC), a lncRNA overexpressed in hepatocellular carcinoma (HCC), has been demonstrated to be involved in the carcinogenesis and progression of HCC. However, the mechanisms of HULC promoting the abnormal growth of HCC cells are still not well elucidated. In the present study, we for the first time demonstrated that HULC promoted the growth of HCC cells through elevating COX-2 protein. Moreover, the study of the corresponding mechanism by which HULC upregulated COX-2 showed that HULC enhanced the level of ubiquitin-specific peptidase 22 (USP22), which decreased ubiquitin-mediated degradation of COX-2 protein by removing the conjugated polyubiquitin chains from COX-2 and finally stabilized COX2 protein. In addition, knockdown of USP22 or COX-2 attenuated HULC-mediated abnormal growth of HCC cells. In conclusion, our results demonstrated that "USP22/COX-2" axis played an important role in HULC promoting growth of HCC cells. The identification of this novel pathway may pave a road for developing new potential anti-HCC strategies.
肝癌中高度上调的长链非编码RNA(lncRNA)——肝癌高表达转录本(HULC),在肝细胞癌(HCC)中过表达,已被证明参与了HCC的发生和发展。然而,HULC促进HCC细胞异常生长的机制仍未完全阐明。在本研究中,我们首次证明HULC通过提高COX-2蛋白水平促进HCC细胞生长。此外,对HULC上调COX-2的相应机制研究表明,HULC提高了泛素特异性蛋白酶22(USP22)的水平,USP22通过从COX-2上去除共轭多聚泛素链,减少泛素介导的COX-2蛋白降解,最终稳定COX-2蛋白。此外,敲低USP22或COX-2可减弱HULC介导的HCC细胞异常生长。总之,我们的结果表明“USP22/COX-2”轴在HULC促进HCC细胞生长中起重要作用。这一新途径的发现可能为开发新的潜在抗HCC策略铺平道路。