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Towards precision medicine: advances in 5-hydroxymethylcytosine cancer biomarker discovery in liquid biopsy

机译:迈向精准医学:液体活检中5-羟甲基胞嘧啶癌症生物标志物的发现进展

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摘要

Robust and clinically convenient biomarkers for cancer diagnosis, early detection, and prognosis have great potential to improve patient survival and are the key to precision medicine. The advent of next-generation sequencing technologies enables a more sensitive and comprehensive profiling of genetic and epigenetic information in tumor-derived materials. Researchers are now able to monitor the dynamics of tumorigenesis in new dimensions, such as using circulating cell-free DNA (cfDNA) and tumor DNA (ctDNA). Mutation-based assays in liquid biopsy cannot always provide consistent results across studies due partly to intra- and inter-tumoral heterogeneity as well as technical limitations. In contrast, epigenetic analysis of patient-derived cfDNA is a promising alternative, especially for early detection and disease surveillance, because epigenetic modifications are tissue-specific and reflect the dynamic process of cancer progression. Therefore, cfDNA-based epigenetic assays are emerging to be a highly sensitive, minimally invasive tool for cancer diagnosis and prognosis with great potential in future precise care of cancer patients. The major obstacle for applying epigenetic analysis of cfDNA, however, has been the lack of enabling techniques with high sensitivity and technical robustness. In this review, we summarized the advances in epigenome-wide profiling of 5-hydroxymethylcytosine (5hmC) in cfDNA, focusing on the detection approaches and potential role as biomarkers in different cancer types.
机译:用于癌症诊断,早期发现和预后的健壮且临床上方便的生物标记物具有改善患者存活率的巨大潜力,并且是精准医学的关键。下一代测序技术的出现使肿瘤来源材料中的遗传和表观遗传信息更加敏感和全面。研究人员现在能够在新的维度上监测肿瘤发生的动态,例如使用循环无细胞DNA(cfDNA)和肿瘤DNA(ctDNA)。液体活检中基于突变的分析不能始终在整个研究中提供一致的结果,部分原因是肿瘤内和肿瘤间的异质性以及技术局限性。相比之下,对患者来源的cfDNA进行表观遗传学分析是一种有前途的选择,尤其是对于早期发现和疾病监测而言,因为表观遗传学修饰是组织特异性的,反映了癌症进展的动态过程。因此,基于cfDNA的表观遗传学检测方法已成为一种高度敏感,微创的癌​​症诊断和预后工具,在未来对癌症患者进行精确护理方面具有巨大潜力。然而,应用cfDNA的表观遗传学分析的主要障碍是缺乏具有高灵敏度和技术稳健性的技术。在这篇综述中,我们总结了cfDNA中5-羟甲基胞嘧啶(5hmC)在表观基因组范围内的研究进展,重点是检测方法和在不同癌症类型中作为生物标志物的潜在作用。

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