RNA-binding protein Trx regulates alternative splicing and promotes metastasis of HCC via interacting with LINC00152

• Published in: Journal of gastroenterology and hepatology 2024-12, Vol.39 (12), p.2892-2902
• Main Authors: Teng, Xiangnan, Shang, Jin, Du, Lingyao, Huang, Wei, Wang, Yonghong, Liu, Miao, Ma, Yuanji, Wang, Ming, Tang, Hong, Bai, Lang
• Format: Article
• Language: English
• Subjects: 1-Phosphatidylinositol 3-kinase; AKT protein; Alternative splicing; Alternative Splicing - genetics; Angiopoietin; Animals; Carcinoma, Hepatocellular - genetics; Carcinoma, Hepatocellular - metabolism; Carcinoma, Hepatocellular - pathology; Carcinoma, Hepatocellular - secondary; Cell Line, Tumor; Cell migration; Cell Movement - genetics; Epithelial-Mesenchymal Transition - genetics; Gene Expression Regulation, Neoplastic; Gene regulation; Genomic analysis; Hepatocellular carcinoma; Humans; Immunoprecipitation; Liver cancer; Liver Neoplasms - genetics; Liver Neoplasms - metabolism; Liver Neoplasms - pathology; Liver Neoplasms - secondary; Metastases; Metastasis; Neoplasm Invasiveness; Neoplasm Metastasis; Original ‐ Hepatology (Experimental); Ribonucleic acid; RNA; RNA, Long Noncoding - genetics; RNA, Long Noncoding - metabolism; RNA-binding protein; RNA-Binding Proteins - genetics; RNA-Binding Proteins - metabolism; Therapeutic targets; Thioredoxin; Thioredoxins - genetics; Thioredoxins - metabolism; Transcriptomes; Up-Regulation; Whole genome sequencing
• ISSN: 0815-9319; 1440-1746; 1440-1746
• DOI: 10.1111/jgh.16735

Epithelial-mesenchymal transition (EMT) is central to HCC metastasis, in which RNA-binding proteins (RBPs) play a key role. To explore the role of RBPs in metastasis of hepatocellular carcinoma (HCC), whole transcriptome sequencing was conducted to identify differential RBPs between HCC with metastasis and HCC without metastasis. The influence of RBPs on metastasis of HCC was verified by in vitro and in vivo experiments. The interaction of RBPs with non-coding RNAs was evaluated by RNA immunoprecipitation and pull-down assays. RNA sequencing, whole-genome sequencing, and alternative splicing analysis were further performed to clarify post-transcriptional regulation mechanisms. Whole transcriptome sequencing results showed that expression of thioredoxin (Trx) was significantly upregulated in HCC patients with metastasis. Trx was also found to be associated with poor prognosis in HCC patients. Overexpression of Trx could promote migration and invasion of HCC cells in vitro and increase the rate of lung metastasis of HCC cells in vivo. Moreover, binding assays showed that Trx could bind to LINC00152. As a result, LINC00152 was verified to determine the pro-metastasis function of Trx by knockdown assay. Furthermore, we revealed that Trx could regulate metastasis-associated alternative splicing program. Specifically, angiopoietin 1 (ANGPT1) was the splicing target; the splicing isoform switching of ANGPT1 could activate the PI3K-Akt pathway, upregulate EMT-associated proteins, and promote migration and invasion of HCC cells. We found that Trx could interact with LINC00152 and promote HCC metastasis via regulating alternative splicing, indicating that Trx may serve as a novel therapeutic target for HCC treatment.