| Revista: | Genetics and molecular biology |
| Base de datos: | PERIÓDICA |
| Número de sistema: | 000459181 |
| ISSN: | 1415-4757 |
| Autores: | Xu, Rui1 He, Haitao1 Wang, Yue1 Peng, Qi1 Mei, Ke1 Liu, Yan1 Yang, Qing1 |
| Instituciones: | 1Jilin University, College of Basic Medical Sciences, Changchun, Jilin. China |
| Año: | 2023 |
| Periodo: | Ene |
| Volumen: | 46 |
| Número: | 2 |
| País: | Brasil |
| Idioma: | Inglés |
| Tipo de documento: | Artículo |
| Enfoque: | Experimental, analítico |
| Resumen en inglés | Long non-coding RNA AK001796 was initially identified altered in lung cancer. Recent research showed it could participate in the prognosis of hepatocellular carcinoma (HCC). However, the general biological role of AK001796 and its underlying mechanisms in HCC remain unclear. Here we demonstrated that the expression level of AK001796 in HCC tissues and cell lines was up-regulated. Silencing AK001796 suppressed the proliferation ability of HCC cells. Through dual luciferase reporter assays and loss/gain of functions studies, we identified that AK001796 could bind to miR-150, a star microRNA, promoting HCC proliferation. Furthermore, it was reported that growth factor receptor binding protein 2-associated binder 1 (GAB1) is a target gene of miR-150. Owing to AK001796 being a decoy for miR-150 and binding the same putative sites of miR-150 as GAB1, we presented that inhibition of miR-150 in AK001796 silencing cells reversed the reduction in GAB1. Subsequently, our findings demonstrated that silencing AK001796 can impair phospho-ERK1/2 and phospho-AKT. In conclusion, our investigation revealed that AK001796 promoted proliferation by enhancing phospho-ERK1/2 and phospho-AKT through AK001796/miR-150/GAB1 axis in HCC. These results provided further evidence for the critical roles of AK001796 accumulating HCC and suggested that AK001796 might act as an HCC biomarker in clinical treatment |
| Disciplinas: | Biología, Medicina |
| Palabras clave: | Oncología, Genética, Carcinoma hepatocelular, Cáncer, ARN |
| Keyword: | Oncology, Genetics, Hepatocellular carcinoma, RNA, Cancer |
| Texto completo: | Texto completo (Ver HTML) Texto completo (Ver PDF) |
