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Circulating microRNA‐590‐5p functions as a liquid biopsy marker in non‐small cell lung cancer

机译:循环microRNA‐590-5p在非小细胞肺癌中充当液体活检标记

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摘要

Despite the availability of various diagnostic procedures, a tissue biopsy is still indispensable for the routine diagnosis of lung cancer. However, inaccurate diagnoses can occur, leading to inefficient cancer management. In this context, use of circulating micro s (mi s) may serve as diagnostic tools as liquid biopsies, and as biomarkers to better understand the molecular mechanisms involved in the progression of cancer. We identified miR‐590‐5p as a potential prognostic marker in the progression of non‐small cell lung cancer ( ). We were able to detect this mi in blood plasma samples of patients through quantitative real‐time . Our data showed an ~7.5‐fold downregulation of miR‐590‐5p in patients compared to healthy controls, which correlated with several clinicopathological features. Further, overexpression of miR‐590‐5p led to decreased cell viability, proliferation, colony formation, migration, and invasion potential of lung cancer cells, whereas its knockdown showed the opposite effect. In addition, the levels of several proteins involved in the epithelial‐to‐mesenchymal transition negatively correlated with miR‐590‐5p levels in lung adenocarcinoma cells and tumors of patients. Further, dual‐luciferase reporter assays identified as a direct target of miR‐590‐5p, which negatively regulated 3 activation and its downstream signaling molecules (eg, Cyclin D1, c‐Myc, Vimentin, and β‐catenin) involved in tumorigenesis. Taken together, our study suggests that miR‐590‐5p functions as a tumor suppressor in through regulating the 3 pathway, and may serve as a useful biomarker for the diagnosis/prognosis of , and as a potential therapeutic target for the treatment of .
机译:尽管可以使用各种诊断程序,但对于肺癌的常规诊断而言,组织活检仍然是必不可少的。但是,可能会发生错误的诊断,从而导致癌症治疗效率低下。在这种情况下,使用循环微秒(mi s)可以作为液体活检的诊断工具,也可以作为生物标记物,以更好地了解癌症发展过程中涉及的分子机制。我们确定了miR‐590-5p是非小细胞肺癌进展的潜在预后标志物()。通过定量实时分析,我们能够在患者的血浆样本中检测到该mi。我们的数据显示,与健康对照组相比,患者的miR-590-5p下调约7.5倍,这与一些临床病理特征相关。此外,miR-590-5p的过表达导致肺癌细胞的细胞活力,增殖,集落形成,迁移和侵袭能力降低,而其敲低则显示相反的效果。另外,参与上皮-间充质转化的几种蛋白质的水平与肺腺癌细胞和患者肿瘤中的miR-590-5p水平呈负相关。此外,双荧光素酶报告基因测定被确定为miR-590-5p的直接靶标,它负调控了3激活及其参与肿瘤发生的下游信号分子(例如,Cyclin D1,c-Myc,Vimentin和β-catenin)。综上所述,我们的研究表明miR‐590‐5p通过调节3途径发挥抑癌作用,并可能作为诊断/预后的有用生物标志物,并可能作为治疗的潜在靶标。

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