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Circular RNA SMO sponges miR-338-3p to promote the growth of glioma by enhancing the expression of SMO

机译:环状RNA SMO海绵可通过增强SMO的表达来促进miR-338-3p促进神经胶质瘤的生长

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摘要

Glioma is one of the most common tumors in the brain and complete cure still a challenge. The present research aimed to investigate the molecular mechanism of circular RNA SMO (circSMO742) in glioma, via targeting miR-338-3p and regulating SMO expression. QRT-PCR was utilized to examine the expression profiles of circSMO742 and microRNA-338-3p (miR-338-3p) in glioma. SMO protein in glioma was tested via western blot. RNA pulldown assay and dual luciferase reporter assays were used to explore the targeting correlation between RNAs. MTT assay, transwell assays and flow cytometry were used to investigate cell proliferation, migration and invasion, and apoptosis, respectively. Tumor xenograft was done to ascertain the effect of circSMO742 knocking down on tumor growth. CircSMO742 and SMO were highly expressed in glioma tissues, while miR-338-3p expression was reduced. CircSMO742 together with SMO could promote cells proliferation, migration and invasion while inhibit cells apoptosis, whereas miR-338-3p showed negative impacts on the cell activity. Knocking down of circSMO742 suppressed glioma growing . CircSMO742 promoted glioma growth by sponging miR-338-3p to regulate SMO expression. Our research revealed a new molecular mechanism of glioma growth and provide a fresh perspective on circRNAs in glioma progression.
机译:胶质瘤是脑中最常见的肿瘤之一,完全治愈仍然是一个挑战。本研究旨在通过靶向miR-338-3p和调节SMO表达来研究神经胶质瘤中环状RNA SMO(circSMO742)的分子机制。 QRT-PCR用于检查circSMO742和microRNA-338-3p(miR-338-3p)在神经胶质瘤中的表达情况。通过蛋白质印迹检测神经胶质瘤中的SMO蛋白。 RNA下拉测定法和双重荧光素酶报告基因测定法用于探索RNA之间的靶向相关性。使用MTT法,transwell法和流式细胞术分别研究细胞增殖,迁移和侵袭以及凋亡。进行肿瘤异种移植以确定circSMO742敲低对肿瘤生长的影响。 CircSMO742和SMO在神经胶质瘤组织中高表达,而miR-338-3p表达降低。 CircSMO742与SMO一起可以促进细胞增殖,迁移和侵袭,同时抑制细胞凋亡,而miR-338-3p则对细胞活性产生负面影响。敲除circSMO742可抑制神经胶质瘤的生长。 CircSMO742通过使miR-338-3p海绵化以调节SMO表达来促进神经胶质瘤的生长。我们的研究揭示了神经胶质瘤生长的新分子机制,并为神经胶质瘤进展中的circRNA提供了新的视角。

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