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Long Noncoding RNA LINC01133 Functions as an miR-422a Sponge to Aggravate the Tumorigenesis of Human Osteosarcoma

机译:长的非编码RNA LINC01133用作miR-422a海绵,以加剧人骨肉瘤的肿瘤鉴定

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摘要

Long noncoding RNAs (lncRNAs) have been verified to participate in various types of malignant tumors, including osteosarcoma (OS), which is the most common primary bone tumor with outstanding morbidity. Although an increasing number of lncRNAs have been reported to mediate the occurrence of OS, the potential mechanisms are still unclear. This study intends to uncover the mechanism by which lncRNA LINC01133 functions as an miRNA sponge to mediate OS tumorigenicity. In this study, we found that the expression level of LINC01133 was statistically upregulated in OS tumor tissue and cell lines compared to noncancerous tissues and a normal human osteoplastic cell line. LINC01133 silencing could also observably suppress the proliferation. migration, and invasion of OS cells (HOS and U2-OS). Bioinformatics analysis predicted that LINC01133 specifically targeted miR-422a, which was validated by dual-luciferase reporter assay. Furthermore, functional experiments revealed that miR-422a played a tumor-suppressive role in OS progression and could effectively reverse the function of LINC01133. In summary. our study discovered that lncRNA LINC01133 aggravates the proliferation, migration, and invasion of OS by sponging miR-422a, which provides a novel insight in the tumorigenesis of OS.
机译:已经验证了长的非分量RNA(LNCRNA)以参与各种类型的恶性肿瘤,包括骨肉瘤(OS),这是具有突出发病率的最常见的原发性骨肿瘤。虽然据报道越来越多的LNCRNA来调解OS的发生,但潜在的机制仍然不清楚。本研究旨在揭示LNCRNA LINC01133用作MiRNA海绵的机制,以介导OS瘤瘤性。在本研究中,我们发现,与非癌组织和正常人骨质塑料细胞系相比,在OS肿瘤组织和细胞系中,LINC01133的表达水平在OS肿瘤组织和细胞系中进行了统计学上上调。 LINC01133沉默也可以识别抑制增殖。迁移和侵入OS单元格(HOS和U2-OS)。生物信息学分析预测LINC01133特异性靶向miR-422a,由双荧光素酶报告验证验证。此外,功能实验表明,MIR-422A在OS进展中发挥了肿瘤抑制作用,可以有效地逆转LINC01133的功能。总之。我们的研究发现,LNCRNA LINC01133通过海绵MIR-422A加剧了OS的增殖,迁移和侵袭,这在OS的肿瘤内提供了新的洞察力。

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