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Long noncoding RNA NEAT1 regulates the development of osteosarcoma through sponging miR‐34a‐5p to mediate HOXA13 expression as a competitive endogenous RNA

机译:长度非编码RNA Neat1通过海绵miR-34a-5p调节骨肉瘤的发育,将Hoxa13表达介导作为竞争内源性RNA

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摘要

Abstract Background Long noncoding RNA (lncRNA) exerts a potential regulatory role in tumorigenesis. LncRNA NEAT1 expression remains high in osteosarcoma tissues. However, its biological mechanism in osteosarcoma remains unknown. Methods In this study, NEAT1 expression in osteosarcoma cells was detected by qRT‐PCR. Proliferative and apoptosis potentials of osteosarcoma cells were determined by CCK‐8 assay and Flow Cytometry, respectively. We identified the potential target of NEAT1 through bioinformatics and dual‐luciferase reporter gene assay. Furthermore, their interaction and functions in regulating the development of osteosarcoma were clarified by Western blot and RIP assay. Results Our results demonstrated a high expression of NEAT1 in osteosarcoma tissues and cells. Overexpression of NEAT1 markedly accelerated proliferative and reduced apoptosis potentials of osteosarcoma cells. Besides, NEAT1 could positively regulate the expression of HOXA13 by competing with miR‐34a‐5p. Conclusion These results indicated that NEAT1 participated in the development of osteosarcoma as a ceRNA to competitively bind to miR‐34a‐5p and thus mediate HOXA13 expression.
机译:摘要背景长度非码RNA(LNCRNA)在肿瘤发生中发挥潜在的调节作用。在骨肉瘤组织中,LNCRNA Neat1表达仍然高。然而,其在骨肉瘤中的生物学机制仍然未知。该研究的方法,通过QRT-PCR检测骨肉瘤细胞中的Neat1表达。通过CCK-8测定和流式细胞术分别测定骨肉瘤细胞的增殖和凋亡电位。我们通过生物信息学和双荧光素酶报告基因测定鉴定了整齐1的潜在靶标。此外,通过蛋白质印迹和RIP测定阐明了调节骨肉瘤的发展的相互作用和功能。结果我们的结果表明,骨肉瘤组织和细胞中的Neat1高表达。 Neat1的过度表达明显加速增殖和降低骨肉瘤细胞的细胞凋亡潜力。此外,Neat1可以通过与miR-34a-5p竞争来积极调节Hoxa13的表达。结论这些结果表明,Neat1参与了骨肉瘤的发展,作为Cerna,以竞争地结合miR-34a-5p,从而介导Hoxa13表达。

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