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首页> 外文期刊>Clinical cancer research: an official journal of the American Association for Cancer Research >Comprehensive genome methylation analysis in bladder cancer: identification and validation of novel methylated genes and application of these as urinary tumor markers.
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Comprehensive genome methylation analysis in bladder cancer: identification and validation of novel methylated genes and application of these as urinary tumor markers.

机译:膀胱癌的全面基因组甲基化分析:新甲基化基因的鉴定和验证,并将其作为泌尿系统肿瘤标记物。

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PURPOSE: Epigenetic alterations are common and can now be addressed in a parallel fashion. We investigated the methylation in bladder cancer with respect to location in genome, consistency, variation in metachronous tumors, impact on transcripts, chromosomal location, and usefulness as urinary markers. EXPERIMENTAL DESIGN: A microarray assay was utilized to analyze methylation in 56 samples. Independent validation was conducted in 63 samples by a PCR-based method and bisulfite sequencing. The methylation levels in 174 urine specimens were quantified. Transcript levels were analyzed using expression microarrays and pathways were analyzed using dedicated software. RESULTS: Global methylation patterns were established within and outside CpG islands. We validated methylation of the eight tumor markers genes ZNF154 (P < 0.0001), HOXA9 (P < 0.0001), POU4F2 (P < 0.0001), EOMES (P = 0.0005), ACOT11 (P = 0.0001), PCDHGA12 (P = 0.0001), CA3 (P = 0.0002), and PTGDR (P = 0.0110), the candidate marker of disease progression TBX4 (P < 0.04), and other genes with stage-specific methylation. The methylation of metachronous tumors was stable and targeted to certain pathways. The correlation to expression was not stringent. Chromosome 21 showed most differential methylation (P < 0.0001) and specifically hypomethylation of keratins, which together with keratin-like proteins were epigenetically regulated. In DNA from voided urine, we detected differential methylation of ZNF154 (P < 0.0001), POU4F2 (P < 0.0001), HOXA9 (P < 0.0001), and EOMES (P < 0.0001), achieving 84% sensitivity and 96% specificity. CONCLUSIONS: We initiated a detailed mapping of the methylome in metachronous bladder cancer. Novel genes with tumor, chromosome, as well as pathway-specific differential methylation in bladder cancer were identified. The methylated genes were promising cancer markers for early detection of bladder cancer.
机译:目的:表观遗传改变很普遍,现在可以并行解决。我们就基因组中的位置,一致性,异时性肿瘤的变异,对转录本的影响,染色体的位置以及作为尿液标记物的用途等方面,研究了膀胱癌中的甲基化。实验设计:利用微阵列分析法分析了56个样品中的甲基化。通过基于PCR的方法和亚硫酸氢盐测序对63个样品进行了独立验证。定量了174个尿液样本中的甲基化水平。使用表达微阵列分析转录物水平,并使用专用软件分析途径。结果:CpG岛内外建立了全球甲基化模式。我们验证了八个肿瘤标记基因ZNF154(P <0.0001),HOXA9(P <0.0001),POU4F2(P <0.0001),EOMES(P = 0.0005),ACOT11(P = 0.0001),PCDHGA12(P = 0.0001)的甲基化,CA3(P = 0.0002)和PTGDR(P = 0.0110),疾病进展TBX4(P <0.04)以及其他具有阶段特异性甲基化的基因的候选标记。异时性肿瘤的甲基化稳定并靶向某些途径。与表达的相关性并不严格。 21号染色体显示出差异最大的甲基化(P <0.0001),特别是角蛋白的低甲基化,后者与角蛋白样蛋白一起受到表观遗传调控。在排空尿液的DNA中,我们检测到ZNF154(P <0.0001),POU4F2(P <0.0001),HOXA9(P <0.0001)和EOMES(P <0.0001)的差异甲基化,实现了84%的敏感性和96%的特异性。结论:我们启动了甲基化组在异时性膀胱癌中的详细定位。在膀胱癌中鉴定了具有肿瘤,染色体以及途径特异性差异甲基化的新基因。甲基化的基因是早期发现膀胱癌的有希望的癌症标志物。

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