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微小RNA-409-3p通过靶向骨肉瘤中的E74样因子2来调节细胞增殖和肿瘤生长。

MiR-409-3p regulates cell proliferation and tumor growth by targeting E74-like factor 2 in osteosarcoma.

作者信息

Zhang Jun, Hou Wengen, Jia Jinling, Zhao Yilei, Zhao Bin

机构信息

Department of Orthopaedics The First Affiliated Hospital of Xinxiang Medical College Weihui Henan China.

出版信息

FEBS Open Bio. 2017 Jan 27;7(3):348-357. doi: 10.1002/2211-5463.12177. eCollection 2017 Mar.

Abstract

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.

摘要

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。

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