Zhang Jun, Hou Wengen, Jia Jinling, Zhao Yilei, Zhao Bin
Department of Orthopaedics The First Affiliated Hospital of Xinxiang Medical College Weihui Henan China.
FEBS Open Bio. 2017 Jan 27;7(3):348-357. doi: 10.1002/2211-5463.12177. eCollection 2017 Mar.
Recent evidence has shown that miR-409-3p was down-regulated in several types of cancer, including osteosarcoma. However, the potential role of miR-409-3p in osteosarcoma remains largely unknown. In the present study, we showed that overexpression of miR-409-3p in osteosarcoma cells inhibited cell proliferation and suppressed tumor growth , and the restoration of miR-409-3p promoted G1/S cell cycle arrest and induced cell apoptosis. Additionally, E74-like factor 2 (ELF2) was recognized as a new target of miR-409-3p by dual-luciferase reporter assay. Restoration of ELF2 rescued the inhibitory effect of miR-409-3p on cell proliferation in osteosarcoma cells. Moreover, ELF2 was up-regulated in osteosarcoma tissues and negatively associated with miR-409-3p levels. Taken together, our findings collectively indicate that miR-409-3p may be a tumor suppressor in osteosarcoma and may serve as a promising therapeutic target for osteosarcoma.
最近的证据表明,miR-409-3p在包括骨肉瘤在内的几种癌症中表达下调。然而,miR-409-3p在骨肉瘤中的潜在作用仍 largely unknown。在本研究中,我们发现骨肉瘤细胞中miR-409-3p的过表达抑制细胞增殖并抑制肿瘤生长,miR-409-3p的恢复促进G1/S细胞周期阻滞并诱导细胞凋亡。此外,通过双荧光素酶报告基因检测,E74样因子2(ELF2)被确认为miR-409-3p的新靶点。ELF2的恢复挽救了miR-409-3p对骨肉瘤细胞增殖的抑制作用。此外,ELF2在骨肉瘤组织中上调,且与miR-409-3p水平呈负相关。综上所述,我们的研究结果共同表明,miR-409-3p可能是骨肉瘤中的一种肿瘤抑制因子,有望成为骨肉瘤的治疗靶点。