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首页> 外文期刊>Cancer Management and Research >LncRNA NEAT1/miR-204/NUAK1 Axis is a Potential Therapeutic Target for Non-Small Cell Lung Cancer
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LncRNA NEAT1/miR-204/NUAK1 Axis is a Potential Therapeutic Target for Non-Small Cell Lung Cancer

机译:LNCRNA Neat1 / miR-204 / Nuak1轴是非小细胞肺癌的潜在治疗靶标

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Background:Long non-coding RNA (lncRNA) is a key part of non-coding RNA, and more and more evidence has revealed that it plays a vital role in tumors. NEAT1 is a lncRNA discovered in the early stage. However, it is still unclear whether NEAT1 and miR-204 play a regulatory role in lung cancer (LC). This research aimed to determine the biological function of NEAT1/miR-204 in non-small cell lung cancer (NSCLC).Materials and Methods:In order to research the function of NEAT1 in NSCLC, RT-PCR, Western blot, luciferase assay and RNA immunoprecipitation assay were used to determine the relationship between NEAT1, miR-204 and NUAK1. CCK8 test, cell migration and invasion test were used to explore the influence of NEAT1 on proliferation and metastasis of LC cells. Tumor allotransplantation was used to detect the influence of NEAT1 on the growth of LC.Results:The results revealed that NEAT1 was obviously enhanced in LC cell lines. Further functional analysis showed that low expression of NEAT1 obviously suppressed the growth, migration and invasion of NSCLC and facilitated cell apoptosis. Determination of luciferase reporter gene revealed that miR-204 was the direct target of NEAT1 in LC. In addition, NUAK1 was called the direct target of miR-204, and miR-204/NUAK1 had saved the role of NEAT1 in NSCLC cells. Tumor allotransplantation experiments showed that knocking down NEAT1 could inhibit the growth of LC.Conclusion:In summary, our results showed that the down-regulation of NEAT1 in NSCLC inhibited its growth, migration and invasion through the miR-204/NUAK1 axis.? 2020 Zhao et al.
机译:背景:长期非编码RNA(LNCRNA)是非编码RNA的关键部分,越来越多的证据表明它在肿瘤中起着至关重要的作用。 neat1是早期发现的lncrana。然而,尚不清楚neat1和miR-204是否在肺癌(LC)中发挥调节作用。该研究旨在确定Neat1 / miR-204在非小细胞肺癌(NSCLC)中的生物学功能。材料和方法:为了研究Neat1在NSCLC,RT-PCR,Western印迹,荧光素酶测定中的功能使用RNA免疫沉淀测定法测定Neat1,miR-204和Nuak1之间的关系。 CCK8测试,细胞迁移和侵袭试验用于探讨Neat1对LC细胞增殖和转移的影响。肿瘤同种异体持续物用于检测Neat1对LC.Results的生长的影响:结果表明,LC细胞系中明显增强了Neat1。进一步的功能分析表明,NEAT1的低表达明显抑制了NSCLC的生长,迁移和侵袭和促进细胞凋亡。荧光素酶报告基因的测定表明,miR-204是LC中Neat1的直接靶标。此外,Nuak1称为miR-204的直接靶标,MiR-204 / Nuak1挽救了Neat1在NSCLC细胞中的作用。肿瘤同种异体化实验表明,敲击凝固液体可以抑制LC.Conclusion的生长:总之,我们的结果表明,NSCLC中Neat1的下调抑制了通过MiR-204 / Nuak1轴的生长,迁移和侵袭。? 2020 Zhao等。

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