LncRNA CSMD1-1 promotes the progression of Hepatocellular Carcinoma by activating MYC signaling

被引:28
|
作者
Liu, Ji [1 ,2 ]
Xu, Rui [3 ]
Mai, Shi-Juan [1 ,2 ]
Ma, Yu-Shui [4 ]
Zhang, Mei-Yin [1 ,2 ]
Cao, Ping-Sheng [4 ]
Weng, Nuo-Qing [1 ,2 ]
Wang, Rui-Qi [1 ,2 ]
Cao, Di [1 ,2 ]
Wei, Wei [5 ]
Guo, Rong-Ping [5 ]
Zhang, Yao-Jun [5 ]
Xu, Li [5 ]
Chen, Min-Shan [5 ]
Zhang, Hui-Zhong [6 ]
Huang, Long [7 ]
Fu, Da [4 ]
Wang, Hui-Yun [1 ,2 ]
机构
[1] Sun Yat Sen Univ, Ctr Canc, State Key Lab Oncol South China, Guangzhou 510060, Peoples R China
[2] Sun Yat Sen Univ, Ctr Canc, Collaborat Innovat Ctr Canc Med, Guangzhou 510060, Peoples R China
[3] Guangzhou Med Univ, Affiliated Canc Hosp & Inst, Guangzhou 510095, Peoples R China
[4] Tongji Univ, Sch Med, Shanghai Peoples Hosp 10, Cent Lab Med Res, Shanghai, Peoples R China
[5] Sun Yat Sen Univ, Ctr Canc, Dept Hepatobiliary Surg, Guangzhou 510060, Peoples R China
[6] Sun Yat Sen Univ, Ctr Canc, Dept Pathol, Guangzhou 510060, Peoples R China
[7] Nanchang Univ, Affiliated Hosp 2, Dept Oncol, Nanchang, Peoples R China
来源
THERANOSTICS | 2020年 / 10卷 / 17期
基金
中国国家自然科学基金;
关键词
Long noncoding RNA; lncCSMD1-1; Hepatocellular carcinoma; MYC; prognosis; C-MYC; GLYCOLYTIC METABOLISM; CANCER; AMPLIFICATION; EXPRESSION; LIVER; P53; PROLIFERATION; INTERACTS; LESIONS;
D O I
10.7150/thno.45989
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Emerging evidence suggests that long non-coding RNAs (lncRNA) play critical roles in the development and progression of diverse cancers including hepatocellular carcinoma (HCC), but the underlying molecular mechanisms of lncRNAs that are involved in hepatocarcinogenesis have not been fully explored. Methods: In this study, we profiled lncRNA expression in 127 pairs of HCC and nontumor liver tissues (a Discovery Cohort) using a custom microarray. The expression and clinical significance of lncCSMD1-1 were then validated with qRT-PCR and COX regression analysis in a Validation Cohort (n=260) and two External Validation Cohorts (n=92 and n=124, respectively). In vitro and in vivo assays were performed to explore the biological effects of lncCSMD1-1 on HCC cells. The interaction of lncCSMD1-1 with MYC was identified by RNA pull-down and RNA immunoprecipitation. The role of LncCSMD1-1 in the degradation of MYC protein was also investigated. Results: With microarray, we identified a highly upregulated lncRNA, lncCSMD1-1, which was associated with tumor progression and poor prognosis in the Discovery Cohort, and validated in another 3 HCC cohorts. Consistently, ectopic expression of lncCSMD1-1 notably promotes cell proliferation, migration, invasion, tumor growth and metastasis of HCC cells in in vitro and in vivo experiments. Gene expression profiling on HCC cells and gene sets enrichment analysis indicated that the MYC target gene set was significantly enriched in HCC cells overexpressing lncCSMD1-1, and lncCSMD1-1 was found to directly bind to MYC protein in the nucleus of HCC cells, which resulted in the elevation of MYC protein. Mechanistically, lncCSMD1-1 interacted with MYC protein to block its ubiquitin-proteasome degradation pathway, leading to activation of its downstream target genes. Conclusion: lncCSMD1-1 is upregulated in HCC and promotes progression of HCC by activating the MYC signaling pathway. These results provide the evidence that lncCSMD1-1 may serve as a novel prognostic marker and potential therapeutic target for HCC.
引用
收藏
页码:7527 / 7544
页数:18
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