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MicroRNA-376c Inhibits Cell Proliferation and Invasion in Osteosarcoma by Targeting to Transforming Growth Factor-Alpha

机译:MicroRNA-376c通过靶向转化生长因子-α抑制骨肉瘤中的细胞增殖和侵袭

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摘要

MicroRNAs are a class of small noncoding RNAs that function as critical gene regulators through targeting mRNAs for translational repression or degradation. In this study, we showed that miR-376c expression level was decreased while transforming growth factor-alpha (TGFA) mRNA expression levels were increased in osteosarcoma tissues and cell lines, and we identified TGFA as a novel direct target of miR-376c. Overexpression of miR-376c suppressed TGFA expression and the expression of its downstream signaling molecule such as epidermal growth factor receptor, and attenuated cell proliferation and invasion. Forced expression of TGFA could partly rescue the inhibitory effect of miR-376c in the cells. Taken together, these findings will shed light on the role and mechanism of miR-376c in regulating osteosarcoma cell growth via miR-376c/TGFA axis, and miR-376c may serve as a potential therapeutic target in osteosarcoma in the future.
机译:MicroRNA是一类小的非编码RNA,它们通过靶向mRNA进行翻译抑制或降解来充当关键的基因调节剂。在这项研究中,我们表明骨肉瘤组织和细胞系中miR-376c的表达水平降低而转化生长因子α(TGFA)mRNA的表达水平升高,并且我们确定TGFA是miR-376c的新型直接靶标。 miR-376c的过表达抑制了TGFA及其下游信号分子如表皮生长因子受体的表达,并减弱了细胞的增殖和侵袭。 TGFA的强制表达可以部分挽救miR-376c在细胞中的抑制作用。综上所述,这些发现将阐明miR-376c在通过miR-376c / TGFA轴调节骨肉瘤细胞生长中的作用和机制,并且miR-376c将来可能成为骨肉瘤的潜在治疗靶标。

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