lncRNA HULC promotes the growth of hepatocellular carcinoma cells via stabilizing COX-2 protein

被引:84
作者
Xiong, Haojun [1 ]
Li, Bo [1 ]
He, Jintao [2 ]
Zeng, Yijun [1 ]
Zhang, Yan [1 ]
He, Fengtian [1 ]
机构
[1] Third Mil Med Univ, Coll Basic Med Sci, Dept Biochem & Mol Biol, Chongqing 400038, Peoples R China
[2] Third Mil Med Univ, Coll Prevent Med, Battal Students 17, Chongqing 400038, Peoples R China
基金
中国国家自然科学基金;
关键词
HULC; HCC; COX-2; USP22; Tumor growth; LONG NONCODING RNA; EPITHELIAL-MESENCHYMAL TRANSITION; CYCLOOXYGENASE-2; EXPRESSION; CANCER; USP22; PROLIFERATION; INVASION; OVEREXPRESSION; METASTASIS; PROGNOSIS;
D O I
10.1016/j.bbrc.2017.06.103
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
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. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:693 / 699
页数:7
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