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首页> 外文期刊>DNA and Cell Biology >hsa_circ_0000177-miR-638-FZD7-Wnt Signaling Cascade Contributes to the Malignant Behaviors in Glioma
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hsa_circ_0000177-miR-638-FZD7-Wnt Signaling Cascade Contributes to the Malignant Behaviors in Glioma

机译:HSA_CIRC_0000177-MIR-638-FZD7-WNT信号级联有助于胶质瘤的恶性行为有助于恶性行为

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As a new member of the noncoding RNA family, circular RNAs (circRNAs) have been demonstrated as critical regulators in various physiological and pathological processes, such as tumorigenesis. However, the role of circRNAs has not been well understood until now. In our study, we found that circRNA hsa_circ_0000177 was upregulated in glioma tissues and cell lines. Also, hsa_circ_0000177 overexpression was associated with poor prognosis in glioma patients. Through functional experiments, we found that hsa_circ_0000177 knockdown dramatically inhibited glioma cell proliferation and invasion in vitro. Consistently, hsa_circ_0000177 knockdown significantly repressed glioma growth in vivo. In terms of mechanism, we used bioinformatics analysis and identified hsa_circ_0000177 as a miR-638 sponge. We showed that miR-638 inhibition could restore the proliferation and invasion of glioma cells transfected with hsa_circ_0000177 small interfering RNA. Furthermore, we demonstrated that frizzled class receptor 7 (FZD7) was targeted by miR-638 and upregulated by hsa_circ_0000177. Through upregulating FZD7 expression, hsa_circ_0000177 activated Wnt signaling and facilitated glioma growth. Taken together, our study revealed a novel signaling pathway involved in glioma progression.
机译:作为非编码RNA系列的新成员,已在各种生理和病理过程中被证明圆形RNA(CircrNA)作为临时调节剂,例如肿瘤发生。然而,直到现在,Circrnas的作用并未得到很好的理解。在我们的研究中,我们发现CircRNA HSA_CIRC_0000177在胶质瘤组织和细胞系中上调。此外,HSA_CIRC_0000177过表达与胶质瘤患者的预后不良有关。通过功能实验,我们发现HSA_CIRC_0000177敲低地抑制胶质瘤细胞增殖和体外侵袭。始终如一地,HSA_CIRC_0000177敲低抑制体内的胶质瘤生长。在机制方面,我们使用生物信息学分析并将HSA_CIRC_0000177识别为MIR-638海绵。我们表明MiR-638抑制可以恢复用HSA_CIRC_0000177小干扰RNA转染的胶质瘤细胞的增殖和侵袭。此外,我们证明了Frizzled类受体7(FZD7)由miR-638定位,并通过HSA_CIRC_0000177上调。通过上调FZD7表达,HSA_CIRC_0000177活化WNT信号传导和促进的胶质瘤生长。我们的研究综合,揭示了一种参与胶质瘤进展的新型信号通路。

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