Nanchong central hospital. 97 Renmin South Road, Shunqing district, Nanchong, Sichuan, PR China,
Department of pharmacy, Nanchong central hospital, Sichuan province, 637000, PR China.
Front Biosci (Landmark Ed). 2020 Jun 1;25(10):1901-1912. doi: 10.2741/4884.
Recent studies indicate that MEG3, a long non-coding RNA (lncRNA) and microRNA-184 (miR-184) are abnormally expressed in osteosarcoma (OS). To this end, we show here that MEG3 negatively regulates the expression of miR-184 and down-stream effectors of WNT/β-catenin pathway including β-catenin, T-cell factor 4 (TCF4) and c-MYC. MEG3 overexpression by adenoviral vectors down-regulate proliferation, migration and apoptosis of OS in vitro and restrict the tumor growth in vivo. We also show that the effects of MEG3 can be effectively reversed by miR-184 mimic. Together these studies show that both MEG3 and miR-184 cooperatively regulate the proliferation, migration and apoptosis of OS.
最近的研究表明,长链非编码 RNA(lncRNA)和 microRNA-184(miR-184)在骨肉瘤(OS)中异常表达。为此,我们在这里表明,MEG3 负调控 miR-184 的表达及其下游 WNT/β-catenin 通路效应物,包括β-catenin、T 细胞因子 4(TCF4)和 c-MYC。腺病毒载体过表达 MEG3 可下调 OS 体外的增殖、迁移和凋亡,并限制体内肿瘤生长。我们还表明,miR-184 模拟物可有效逆转 MEG3 的作用。这些研究表明,MEG3 和 miR-184 共同调节 OS 的增殖、迁移和凋亡。