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5-Hydroxymethylcytosine and ten-eleven translocation dioxygenases in head and neck carcinoma

机译:头颈部癌中的5-羟甲基胞嘧啶和十一十一易位双加氧酶

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摘要

Ten-eleven translocation (TET) enzymes are implicated in DNA demethylation through dioxygenase activity, which converts 5-methylcytosine to 5-hydroxymethylcytosine (5-hmC). However, the specific roles of TET enzymes and 5-hmC levels in head and neck squamous cell carcinoma (HNSCC) have not yet been evaluated. In this study, we analyzed 5-hmC levels and TET mRNA expression in a well-characterized dataset of 117 matched pairs of HNSCC tissues and normal tissues. 5-hmC levels and TET mRNA expression were examined via enzyme-linked immunosorbent assay and quantitative real-time PCR, respectively. 5-hmC levels were evaluated according to various clinical characteristics and prognostic implications. Notably, we found that 5-hmC levels were significantly correlated with tumor stage (P = 0.032) and recurrence (P = 0.018). Univariate analysis revealed that low levels of 5-hmC were correlated with poor disease-free survival (DFS; log-rank test, P = 0.038). The expression of TET family genes was not associated with outcomes. In multivariate analysis, low levels of 5-hmC were evaluated as a significant independent prognostic factor of DFS (hazard ratio: 2.352, 95% confidence interval: 1.136-4.896; P = 0.021). Taken together, our findings showed that reduction of TET family gene expression and subsequent low levels of 5-hmC may affect the development of HNSCC.
机译:十一十一易位(TET)酶通过双加氧酶活性参与DNA脱甲基化,该酶将5-甲基胞嘧啶转化为5-羟甲基胞嘧啶(5-hmC)。但是,尚未评估TET酶和5-hmC在头颈部鳞状细胞癌(HNSCC)中的特定作用。在这项研究中,我们分析了特征明确的117对HNSCC组织和正常组织配对的数据集中的5-hmC水平和TET mRNA表达。通过酶联免疫吸附测定和定量实时PCR分别检测5-hmC水平和TET mRNA表达。根据各种临床特征和预后影响评估5-hmC水平。值得注意的是,我们发现5-hmC水平与肿瘤分期(P = 0.032)和复发(P = 0.018)显着相关。单因素分析显示5-hmC水平低与无病生存期差有关(DFS;对数秩检验,P = 0.038)。 TET家族基因的表达与结局无关。在多变量分析中,将低水平的5-hmC评估为DFS的重要独立预后因素(危险比:2.352,95%置信区间:1.136-4.896; P = 0.021)。两者合计,我们的研究结果表明,TET家族基因表达的减少和随后的低水平的5-hmC可能影响HNSCC的发展。

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