Long noncoding RNA CRNDE stabilized by hnRNPUL2 accelerates cell proliferation and migration in colorectal carcinoma via activating Ras/MAPK signaling pathways

• DOI: 10.1038/cddis.2017.258
• Publication Date: 2017-06-08T12:42:52Z
• Authors: Huijuan Jiang; Yiqing Wang; Meiling Ai; Haowei Wang; Zhijiao Duan; Huanan Wang; Li Zhao; Jiang Yu; Yanqing Ding; Shuang Wang
• Keywords: Male; 0301 basic medicine; Mice, Inbred BALB C; MAP Kinase Signaling System; Mice, Nude; Heterogeneous-Nuclear Ribonucleoproteins; 3. Good health; Proto-Oncogene Proteins p21(ras); Mice; 03 medical and health sciences; Cell Movement; Cell Line, Tumor; Animals; Humans; Original Article; Female; RNA, Long Noncoding; RNA, Neoplasm; Colorectal Neoplasms; Extracellular Signal-Regulated MAP Kinases; Cell Proliferation

AbstractRecent studies have furthered our understanding of the function of long noncoding RNAs (lncRNAs) in numerous biological processes, including cancer. This study investigated the expression of a novel lncRNA, colorectal neoplasia differentially expressed (CRNDE), in colorectal carcinoma (CRC) tissues and cells by real-time RT-PCR and in situ hybridization, and its biological function using a series of in vitro and in vivo experiments to determine its potential as a prognostic marker and therapeutic target. CRNDE was found to be upregulated in primary CRC tissues and cells (P<0.05), and the upregulation of CRNDE expression is a powerful predictor of advanced TNM stage (P<0.05) and poor prognosis for CRC patients (P=0.002). The promoting effects of CRNDE on the cell proliferation, cell cycling and metastasis of CRC cells were confirmed both in vitro and in vivo by gain-of-function and loss-of-function experiments. Mechanistically, it was demonstrated that CRNDE could form a functional complex with heterogeneous nuclear ribonucleoprotein U-like 2 protein (hnRNPUL2) and direct the transport of hnRNPUL2 between the nucleus and cytoplasm. hnRNPUL2 that was accumulated in the cytoplasm could interact with CRNDE both physically and functionally, increasing the stability of CRNDE RNA. Moreover, gene expression profile data showed that CRNDE depletion in cells downregulated a series of genes involved in the Ras/mitogen-activated protein kinase signaling pathways. Collectively, these findings provide novel insights into the function and mechanism of lncRNA CRNDE in the pathogenesis of CRC and highlight its potential as a therapeutic target for CRC intervention.