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Down-regulation of lncRNA DNAJC3-AS1 inhibits colon cancer via regulating miR-214-3p/LIVIN axis

机译:LNCRNA DNAJC3-AS1的下调通过调节miR-214-3p / livin轴来抑制结肠癌

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摘要

Long non-coding RNAs (lncRNAs) play a key role in the development and metastasis of cancer. However, the biological role and clinical significance of lncRNA DNAJC3-AS1 in the development of colon cancer is still unknown. In this study, the effects of DNAJC3-AS1 on cell proliferation, migration, and invasion were evaluated by MTT assay, wound-healing assay, and transwell assay, respectively. The relationship between DNAJC3-AS1, miR-214-3p and LIVIN was predicted by the online software and confirmed by dual-luciferase reporter assay. We found that the down-regulation of DNAJC3-AS1 inhibited the proliferation of colon cancer cells and induced growth arrest. Down-regulation of DNAJC3-AS1 also inhibited the migration, invasion, and epithelial-mesenchymal transition (EMT) of colon cancer cells. Moreover, miR-214-3p can bind to DNAJC3-AS1, and knockdown of DNAJC3-AS1 increased miR-214-3p expression in colon cancer cells. LIVIN was identified as a target of miR-214-3p. The up-regulation of miR-214-3p inhibited the protein expression of LIVIN and suppressed the activation of the NF-κB signaling pathway. Besides, down-regulation of DNAJC3-AS1 reduced cell viability, invasion, and EMT of colon cancer cells, while miR-214-3p inhibitor could reverse these effects. The expression of LIVIN and the activation of the NF-κB signaling pathway were suppressed by down-regulating DNAJC3-AS1, while these effects could be restored by miR-214-3p inhibitor. These findings suggested that DNAJC3-AS1 may promote colon cancer progression by regulating the miR-214-3p/LIVIN axis. DNAJC3-AS1 may serve as a new biomarker and therapeutic target for colon cancer, stimulating new research directions and treatment options.
机译:长期非编码RNA(LNCRNA)在癌症的发育和转移中发挥关键作用。然而,LNCRNA DNAJC3-AS1在结肠癌发育中的生物学作用和临床意义仍然未知。在该研究中,通过MTT测定,伤口愈合测定和Transwell测定分别评估DNAJC3-AS1对细胞增殖,迁移和侵袭的影响。通过在线软件预测DNAJC3-AS1,MIR-214-3P和LIVIN之间的关系,并通过双荧光素酶报告分析证实。我们发现DNAJC3-AS1的下调抑制了结肠癌细胞的增殖并诱导生长骤停。 DNAJC3-AS1的下调还抑制了结肠癌细胞的迁移,侵袭和上皮 - 间充质转换(EMT)。此外,MIR-214-3P可以与DNAJC3-AS1结合,并且DNAJC3-AS1的敲低增加了结肠癌细胞中的miR-214-3p表达。 Livin被鉴定为miR-214-3p的目标。 miR-214-3p的上调抑制Livin的蛋白表达并抑制了NF-κB信号通路的激活。此外,DNAJC3-AS1的下调降低细胞活力,侵袭和结肠癌细胞的EMT,而MIR-214-3P抑制剂可以逆转这些效果。通过下调DNAJC3-AS1抑制Livin和NF-κB信号传导途径的活化的表达,而MIR-214-3P抑制剂可以恢复这些效果。这些发现表明DNAJC3-AS1可以通过调节miR-214-3P / Livin轴来促进结肠癌进展。 DNAJC3-AS1可以作为结肠癌的新生物标志物和治疗靶标,刺激新的研究方向和治疗方案。

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