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Downregulation of miR-204 is associated with poor prognosis and promotes cell proliferation in hypopharyngeal squamous cell carcinoma (HSCC)

机译:miR-204的下调与预后不良有关并促进下咽鳞状细胞癌(HSCC)的细胞增殖

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摘要

MircroRNAs (miRNAs) were identified to be involved in tumor progression and prognosis. However, the clinical significance and biological function of miR-204 in hypopharyngeal squamous cell carcinoma (HSCC) are not well appreciated. Therefore, the aim of this study is to explore the role of miR-204 in HSCC. The miR-204 expression was determined in 56 pairs of HSCC tumor and adjacent non-tumor tissues by quantitative real-time reverse transcriptive-PCR (qRT-PCR). Kaplan-Meier survival curve analysis and log-rank test were used to analyze the association between miR-204 expression and clinicopathological parameters and the over survival (OS) time in HSCC patients. Univariate and multivariate Cox analysis was applied to investigate the predicted risk factors for OS. Moreover, CCK8 cell proliferation assays, flow cytometry analysis and western-blot analysis were performed to examine the cell growth and cell cycle related protein expression in FaDu cells. In the study, our results reported that miR-204 was down-regulated in HSCC tissues. The patients with lower miR-204 expression had significantly poor OS time. Multivariable Cox analysis demonstrated that lower miR-204 expression was an independent risk factor in HSCC patients. Furthermore, CCK8 cells assays and cell cycle analysis showed that over-expression of miR-204 significantly inhibited cell proliferation, S phase cell number and inhibited the cell cycle related protein expression of CyclinD1, CDK4 and CDK6, but up-regulated the p21 expression in FaDu cells. Thus, our study demonstrated that miR-204 was downregulated in HSCC and upregulation of miR-204 suppressed cell proliferation, which highlighted that miR-204 could have potential therapeutic applications in HSCC.
机译:MircroRNA(miRNA)被确定与肿瘤的进展和预后有关。但是,miR-204在下咽鳞状细胞癌(HSCC)中的临床意义和生物学功能尚未得到很好的认识。因此,本研究的目的是探讨miR-204在HSCC中的作用。通过定量实时逆转录PCR(qRT-PCR)在56对HSCC肿瘤和邻近的非肿瘤组织中确定了miR-204的表达。使用Kaplan-Meier生存曲线分析和log-rank检验分析miR-204表达与临床病理参数之间的关联以及HSCC患者的生存期(OS)时间。单因素和多因素Cox分析用于研究OS的预测危险因素。此外,进行了CCK8细胞增殖测定,流式细胞术分析和蛋白质印迹分析以检查FaDu细胞中的细胞生长和细胞周期相关蛋白表达。在这项研究中,我们的结果报告了在HSCC组织中miR-204被下调。 miR-204表达较低的患者的OS时间明显较差。多变量Cox分析表明,较低的miR-204表达是HSCC患者的独立危险因素。此外,CCK8细胞分析和细胞周期分析表明,miR-204的过表达显着抑制细胞增殖,S期细胞数量并抑制CyclinD1,CDK4和CDK6的细胞周期相关蛋白表达,但上调p21表达。 FaDu细胞。因此,我们的研究表明,miR-204在HSCC中被下调,而miR-204的上调抑制了细胞增殖,这突显了miR-204在HSCC中可能具有潜在的治疗应用。

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