首页> 美国卫生研究院文献>Clinical Epigenetics >Analysis of RET promoter CpG island methylation using methylation-specific PCR (MSP) pyrosequencing and methylation-sensitive high-resolution melting (MS-HRM): impact on stage II colon cancer patient outcome
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Analysis of RET promoter CpG island methylation using methylation-specific PCR (MSP) pyrosequencing and methylation-sensitive high-resolution melting (MS-HRM): impact on stage II colon cancer patient outcome

机译:使用甲基化特异性PCR(MSP)焦磷酸测序和甲基化敏感的高分辨率熔解(MS-HRM)分析RET启动子CpG岛甲基化:对II期结肠癌患者预后的影响

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摘要

BackgroundAlready since the 1990s, promoter CpG island methylation markers have been considered promising diagnostic, prognostic, and predictive cancer biomarkers. However, so far, only a limited number of DNA methylation markers have been introduced into clinical practice. One reason why the vast majority of methylation markers do not translate into clinical applications is lack of independent validation of methylation markers, often caused by differences in methylation analysis techniques. We recently described RET promoter CpG island methylation as a potential prognostic marker in stage II colorectal cancer (CRC) patients of two independent series.
机译:背景技术自1990年代以来,启动子CpG岛甲基化标记已被认为是有前途的诊断,预后和预测性癌症生物标记。然而,到目前为止,仅有限数量的DNA甲基化标记物已被引入临床实践。绝大多数甲基化标记不能转化为临床应用的原因之一是缺乏甲基化标记的独立验证,这通常是由甲基化分析技术的差异引起的。我们最近将RET启动子CpG岛甲基化描述为两个独立系列的II期结直肠癌(CRC)患者的潜在预后标志物。

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