Xinping Huang1, Jin Hou2, Xiaoyun Shen1, Chao‐Yuan Huang1, Xuehui Zhang1, Yu‐An Xie1, Jiaxiang Ye1
1Research Department, Affiliated Tumor Hospital of Guangxi Medical University, Nanning, China
2National Key Laboratory of Medical Immunology and Institute of Immunology, Second Military Medical University, Shanghai, China
Tóm tắt
Deregulated microRNAs and their roles in carcinogenesis and cancer progression have attracted much attention. In previous studies conducted in our laboratory, the Illumina Solexa massively parallel signature sequencing of miRNomes in nontumor and hepatocellular carcinoma (HCC) tissues revealed that miR‐486‐5p was significantly downregulated in HCC, but its role in HCC development remains unknown. In this study, miR‐486‐5p levels in HCC tissues and matched control tissues, and in seven HCC cell lines (QGY‐7701, QGY‐7703, QGY‐7404, SMMC‐7721, Huh7, HepG2, and PCL/PRF/5) and human normal liver cells (HL‐7702), were tested by real‐time quantitative RT‐PCR. We found that the level of miR‐486‐5p was significantly decreased in HCC tissue and in all seven HCC cell lines. Overexpression of miR‐486‐5p markedly suppressed HCC cell proliferation, migration and invasion in vitro, and inhibited HCC growth in vivo. Mechanistically, miR‐486‐5p was confirmed to directly target PIK3R1 expression, thereby suppressing phosphatidylinositol 3‐kinase–AKT pathway activation, by dual luciferase reporter assay and real‐time quantitative RT‐PCR and western blot analysis. In addition, PIK3R1 knockdown mimicked the effects of miR‐486‐5p overexpression by inhibiting HCC growth, migration, and invasion. Furthermore, correlation analysis, Kaplan–Meier estimates and Cox proportional hazard models showed an inverse correlation between miR‐486‐5p and PIK3R1, as well as a shorter time to recurrence after HCC resection, in patients with lower miR‐486‐5p expression. Hence, we conclude that miR‐486‐5p, which is frequently downregulated in HCC, inhibits HCC progression by targeting PIK3R1 and phosphatidylinositol 3‐kinase–AKT activation.DatabaseThe Solexa sequencing data are available in GEO database (www.ncbi.nlm.nih.gov/geo/) under accession number GSE21279.
