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DNA methylation at the novel CpG sites in the promoter of MED15/PCQAP gene as a biomarker for head and neck cancers

机译:MED15 / PCQAP基因启动子中新CpG位点的DNA甲基化作为头颈癌的生物标记

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摘要

Head and neck cancers (HNCs) represent a significant and ever-growing burden to the modern society, mainly due to the lack of early diagnostic methods. A significant number of HNCs is often associated with drinking, smoking, chewing beetle nut, and human papilloma virus (HPV) infections. We have analyzed DNA methylation patterns in tumor and normal tissue samples collected from head and neck squamous cell carcinoma (HNSCC) patients who were smokers. We have identified novel methylation sites in the promoter of the mediator complex subunit 15 (MED15/PCQAP) gene (encoing a co-factor important for regulation of transcription initiation for promoters of many genes), hypermethylated specifically in tumor cells. Two clusters of CpG dinucleotides methylated in tumors, but not in normal tissue from the same patients, were identified. These CpG methylation events in saliva samples were further validated in a separate cohort of HNSCC patients (who developed cancer due to smoking or HPV infections) and healthy controls using methylation-specific PCR (MSP). We used saliva as a biological medium because of its non-invasive nature, close proximity to the tumors, easiness and it is an economically viable option for large-scale screening studies. The methylation levels for the two identified CpG clusters were significantly different between the saliva samples collected from healthy controls and HNSCC individuals (Welch's t-test returning P, 0.05 and Mann-Whitney test P, 0.01 for both). The developed MSP assays also provided a good discriminative ability with AUC values of 0.70 (P, 0.01) and 0.63 (P, 0.05). The identified novel CpG methylation sites may serve as potential non-invasive biomarkers for detecting HNSCC. © the authors.
机译:头颈癌(HNC)对现代社会构成了沉重且不断增长的负担,这主要是由于缺乏早期诊断方法所致。大量HNC通常与饮酒,吸烟,咀嚼甲虫坚果和人类乳头瘤病毒(HPV)感染有关。我们分析了从吸烟者的头颈部鳞状细胞癌(HNSCC)患者收集的肿瘤和正常组织样本中的DNA甲基化模式。我们已经确定了介体复合物亚基15(MED15 / PCQAP)基因的启动子中新的甲基化位点(编码对调节许多基因的启动子转录起始重要的辅因子),在肿瘤细胞中特异地超甲基化。鉴定出在同一患者的正常组织中肿瘤中甲基化的两个CpG二核苷酸簇。唾液样品中的这些CpG甲基化事件使用甲基化特异性PCR(MSP)在另一组HNSCC患者(由于吸烟或HPV感染而罹患癌症)和健康对照中得到了进一步验证。我们将唾液用作生物介质,因为它具有非侵入性,与肿瘤非常接近,易于操作,并且它是大规模筛选研究的经济上可行的选择。从健康对照组和HNSCC个体收集的唾液样本中,两个鉴定出的CpG簇的甲基化水平显着不同(Welch的t检验返回P,均为0.05,Mann-Whitney检验为P,均为0.01)。发达的MSP测定法还具有良好的判别能力,AUC值分别为0.70(P,0.01)和0.63(P,0.05)。鉴定出的新的CpG甲基化位点可作为潜在的非侵入性生物标志物,用于检测HNSCC。 ©作者。

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