| Literature DB >> 33753989 |
Xiwu Ouyang1, Lemeng Feng2, Guodong Liu3,4, Lei Yao1, Zhiming Wang1, Shiqing Liu5, Yao Xiao1,6, Gewen Zhang1.
Abstract
Hepatocellular carcinoma (HCC) is the most 5th commonly diagnosed and 2nd most lethal tumor in the world. The obvious gender advantage of HCC indicates that androgen receptor (AR) may play an important role in the tumor occurrence, develop and metastasis of HCC. Here we found that decreased AR could alter miR-325 to increase ACP5 expression in HCC cells, to increase HCC cells migration and invasion capacities. Mechanism dissection revealed that AR could regulate miR-325 expression through transcriptional regulation and miR-325 might directly target the 3'UTR of ACP5-mRNA to suppress its translation. The in vivo orthotopic xenografts mouse model with oemiR-325 also validated in vitro data. Together, these findings suggest that AR may decrease HCC progression through miR-325/ACP5 signaling and targeting the AR/miR-325/ACP5 signaling may help in the development of the novel therapies to better suppress the HCC progression. © The author(s).Entities:
Keywords: ACP5; AR; HCC; invasion; miR-325; migration
Year: 2021 PMID: 33753989 PMCID: PMC7974538 DOI: 10.7150/jca.49200
Source DB: PubMed Journal: J Cancer ISSN: 1837-9664 Impact factor: 4.207