Journal Article

A novel lncRNA uc.134 represses hepatocellular carcinoma progression by inhibiting CUL4A-mediated ubiquitination of LATS1

Zhang, Yuqin, Ding, Yi, Liang, Yonghao, Zhan, Zetao, Huang, Jing, Chen, Keli, Ni, Wen, Ye, Feng, Chen, Longhua

2017

Overview

Background Hepatocellular carcinoma (HCC) is one of the most common malignancies worldwide, and tumor recurrence and metastasis are major factors that contribute to the poor outcome of patients with HCC. Long noncoding RNAs (lncRNAs) are known to regulate different tumorigenic processes, and a growing body of evidence indicates that Hippo kinase signaling is inactivated in many cancers. However, the upstream lncRNA regulators of Hippo kinase signaling in HCC are poorly understood. Methods Using a lncRNA microarray, we identified a novel lncRNA, uc.134, whose expression was significantly decreased in the highly aggressive HCC cell line HCCLM3 compared with MHCC97L cells. Furthermore, we evaluated uc.134 expression in clinical samples using in situ hybridization (ISH) and quantitative real-time polymerase chain reaction (qRT-PCR) analysis. The full-length transcript of uc.134 was confirmed using rapid amplification of cDNA ends (RACE) analyses. To investigate the biological function of uc.134, we performed gain-of-function and loss-of-function studies both in vitro and in vivo. The underlying mechanisms of uc.134 in HCC were investigated using RNA pulldown, RNA immunoprecipitation, ubiquitination assays, Western blotting, mRNA microarray analyses, and qRT-PCR analyses. Results The ISH assay revealed that uc.134 expression was significantly decreased in 170 paraffin-embedded samples from patients with HCC compared with adjacent tissues and uc.134 expression directly correlated with patient prognosis. Furthermore, we defined a 1867-bp full-length transcript of uc.134 using 5′- and 3′-RACE analysis. The overexpression of uc.134 inhibited HCC cell proliferation, invasion, and metastasis in vitro and in vivo, whereas the knockdown of uc.134 produced the opposite results. Furthermore, we confirmed that uc.134 (1408–1867 nt) binds to CUL4A (592–759 aa region) and inhibits its nuclear export. Moreover, we demonstrated that uc.134 inhibits the CUL4A-mediated ubiquitination of LATS1 and increases YAP S127 phosphorylation to silence the target genes of YAP. Finally, a positive correlation between uc.134, LATS1, and pYAP S127 was confirmed in 90 paraffin-embedded samples by ISH and immunohistochemical staining. Conclusions Our study identifies that a novel lncRNA, uc.134, represses hepatocellular carcinoma progression by inhibiting the CUL4A-mediated ubiquitination of LATS1 and increasing YAP S127 phosphorylation. The use of this lncRNA may offer a promising treatment approach by inhibiting YAP and activating Hippo kinase signaling.

• Publisher: BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
• Subject: Adaptor Proteins, Signal Transducing - metabolism / Animals / Apoptosis / c-Myc protein / Cancer Research / Cancer therapies / Carcinogenesis / Carcinoma, Hepatocellular - genetics / Carcinoma, Hepatocellular - pathology / Catenin / Cell cycle / Cell growth / Cell Line, Tumor / Cell Proliferation / Cell size / Chemotherapy / Comparative analysis / Computer programs / CUL4A / Cullin Proteins - metabolism / Development and progression / Disease Progression / DNA microarrays / Female / Gene expression / Genomes / Hematology / Hepatocellular carcinoma / Hepatoma / Heterografts / Humans / Hybridization / Immunohistochemistry / Insects / Kinases / LATS1 / Liver cancer / Liver Neoplasms / LncRNA uc.134 / Localization / Macromolecules / Male / Mammals / Medical prognosis / Medicine / Medicine & Public Health / Metastases / Metastasis / Mice / Neoplasm Metastasis / Oncology / Patients / Phosphoproteins - metabolism / Phosphorylation / Prognosis / Protein kinase / Protein Serine-Threonine Kinases - metabolism / Proteins / pYAPS127 / Radiation therapy / RNA / RNA, Long Noncoding - analysis / RNA, Long Noncoding - genetics / RNA, Long Noncoding - metabolism / RNA, Long Noncoding - physiology / Signal transduction / Stem cells / Surgery / Temperature effects / Transcription Factors / Transplantation / Trends / Tumorigenesis / Ubiquitin / Ubiquitination / Ubiquitination - genetics / YAP-Signaling Proteins / Yes-associated protein