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TGFB2 and BCL2L11 methylation in male laryngeal cancer patients

机译:TGFB2和BCL2L11甲基化在男性喉癌患者中

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摘要

DNA methylation is a major regulatory mechanism of gene expression. The aim of the present study was to test the association of transforming growth factor 2 (TGFB2) and B cell lymphoma 2-like 11 (BCL2L11) gene methylation with the risk of laryngeal squamous cell carcinoma (LSCC). Using bisulfite pyrosequencing technology, DNA methylation levels of TGFB2 promoter and BCL2L11 gene-body CpG cytosines were measured in 90 LSCC tissues and 90 adjacent normal tissues. Analysis of variance and paired sample t-test were used to determine the association of gene methylation and the risk of LSCC. Our results revealed that there were no differences in TGFB2 and BCL2L11 methylation levels between the LSCC tissues and the paired normal tissues (P>0.05). Further breakdown analyses demonstrated that the association results of the two gene methylation levels and LSCC remained unchanged with the age, smoking history, histological differentiation or clinical stage of the LSCC patients (all adjusted P>0.05). In conclusion, there is no association of TGFB2 promoter and BCL2L11 gene-body methylation with the risk of LSCC in males.
机译:DNA甲基化是基因表达的主要调控机制。本研究的目的是测试转化生长因子2(TGFB2)和B细胞淋巴瘤2样11(BCL2L11)基因甲基化与喉鳞状细胞癌(LSCC)的风险之间的关系。使用亚硫酸氢盐焦磷酸测序技术,在90个LSCC组织和90个相邻的正常组织中测量了TGFB2启动子和BCL2L11基因体CpG胞嘧啶的DNA甲基化水平。方差分析和配对样本t检验用于确定基因甲基化与LSCC风险的关联。我们的结果表明,在LSCC组织和配对的正常组织之间,TGFB2和BCL2L11甲基化水平没有差异(P> 0.05)。进一步的细分分析表明,两种基因甲基化水平与LSCC的关联结果随LSCC患者的年龄,吸烟史,组织学分化或临床分期而保持不变(所有调整后的P> 0.05)。总之,男性中TGFB2启动子和BCL2L11基因体甲基化与LSCC的风险没有关联。

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