Wu Panfeng, Liang Jieyu, Yu Fang, Zhou Zhengbing, Tang Juyu, Li Kanghua
Department of Orthopedics, Xiang Ya Hospital Central South University, Changsha, Hunan, People's Republic of China.
Oncotarget. 2016 Jul 5;7(27):42241-42251. doi: 10.18632/oncotarget.9948.
Osteosarcoma (OS) is the most common malignant bone tumor in children and young adults. miR-145 is a microRNA highly expressed in vascularized tissues and has been widely studied in cancers. In this study, we explored the expression and function of miR-145 in OS. We found that miR-145 was consistently under-expressed in OS tissues and cell lines as compared to normal bone tissues and osteoblast cells. Ectopic expression of miR-145 in OS cells inhibited their proliferation and migration and induced apoptosis. miR-145 targets a putative microRNA regulatory element (MRE) in the 3'-UTR of friend leukemia virus integration 1 gene (FLI-1), and its abundance was inversely related to FLI-1 expression in OS tissues and cell lines. miR-145 decreased expression FLI-1 protein and mRNA, but mutation of the miR-145 MRE sequence in the FLI-1 3'-UTR abolished the activity of miR-145 in a reporter assay. Restored expression of FLI-1 diminished miR-145-mediated suppression of tumor progression. These results suggest that miR-145 acts as a tumor suppressor by directly reducing expression of FLI-1, and that the miR-145/FLI-1 pathway is important for tumor progression in OS.
骨肉瘤(OS)是儿童和年轻成年人中最常见的恶性骨肿瘤。miR-145是一种在血管化组织中高度表达的微小RNA,并且已在癌症中得到广泛研究。在本研究中,我们探究了miR-145在骨肉瘤中的表达及功能。我们发现,与正常骨组织和成骨细胞相比,miR-145在骨肉瘤组织和细胞系中始终低表达。在骨肉瘤细胞中异位表达miR-145可抑制其增殖和迁移并诱导凋亡。miR-145靶向Friend白血病病毒整合1基因(FLI-1)3'-UTR中的一个假定微小RNA调控元件(MRE),并且其丰度与骨肉瘤组织和细胞系中FLI-1的表达呈负相关。miR-145降低了FLI-1蛋白和mRNA的表达,但在报告基因检测中,FLI-1 3'-UTR中miR-145 MRE序列的突变消除了miR-145的活性。恢复FLI-1的表达可减弱miR-145介导的肿瘤进展抑制作用。这些结果表明,miR-145通过直接降低FLI-1的表达发挥肿瘤抑制作用,并且miR-145/FLI-1通路对骨肉瘤的肿瘤进展很重要。