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DNA甲基化癌症生物标志物:向临床转化

DNA Methylation Cancer Biomarkers: Translation to the Clinic.

作者信息

Locke Warwick J, Guanzon Dominic, Ma Chenkai, Liew Yi Jin, Duesing Konsta R, Fung Kim Y C, Ross Jason P

机构信息

Molecular Diagnostics Solutions, CSIRO Health and Biosecurity, North Ryde, NSW, Australia.

Probing Biosystems Future Science Platform, CSIRO Health and Biosecurity, Canberra, ACT, Australia.

出版信息

Front Genet. 2019 Nov 14;10:1150. doi: 10.3389/fgene.2019.01150. eCollection 2019.

Abstract

Carcinogenesis is accompanied by widespread DNA methylation changes within the cell. These changes are characterized by a globally hypomethylated genome with focal hypermethylation of numerous 5'-cytosine-phosphate-guanine-3' (CpG) islands, often spanning gene promoters and first exons. Many of these epigenetic changes occur early in tumorigenesis and are highly pervasive across a tumor type. This allows DNA methylation cancer biomarkers to be suitable for early detection and also to have utility across a range of areas relevant to cancer detection and treatment. Such tests are also simple in construction, as only one or a few loci need to be targeted for good test coverage. These properties make cancer-associated DNA methylation changes very attractive for development of cancer biomarker tests with substantive clinical utility. Across the patient journey from initial detection, to treatment and then monitoring, there are several points where DNA methylation assays can inform clinical practice. Assays on surgically removed tumor tissue are useful to determine indicators of treatment resistance, prognostication of outcome, or to molecularly characterize, classify, and determine the tissue of origin of a tumor. Cancer-associated DNA methylation changes can also be detected with accuracy in the cell-free DNA present in blood, stool, urine, and other biosamples. Such tests hold great promise for the development of simple, economical, and highly specific cancer detection tests suitable for population-wide screening, with several successfully translated examples already. The ability of circulating tumor DNA liquid biopsy assays to monitor cancer also allows for the ability to monitor response to therapy, to detect minimal residual disease and as an early biomarker for cancer recurrence. This review will summarize existing DNA methylation cancer biomarkers used in clinical practice across the application domains above, discuss what makes a suitable DNA methylation cancer biomarker, and identify barriers to translation. We discuss technical factors such as the analytical performance and product-market fit, factors that contribute to successful downstream investment, including geography, and how this impacts intellectual property, regulatory hurdles, and the future of the marketplace and healthcare system.

摘要

致癌作用伴随着细胞内广泛的DNA甲基化变化。这些变化的特征是基因组整体低甲基化,同时众多5'-胞嘧啶-磷酸-鸟嘌呤-3'(CpG)岛发生局灶性高甲基化,这些岛通常跨越基因启动子和首个外显子。许多此类表观遗传变化在肿瘤发生早期就已出现,并且在多种肿瘤类型中普遍存在。这使得DNA甲基化癌症生物标志物适用于早期检测,并且在与癌症检测和治疗相关的一系列领域中都具有实用性。此类检测在构建上也很简单,因为只需针对一个或几个位点就能实现良好的检测覆盖。这些特性使得与癌症相关的DNA甲基化变化对于开发具有实质临床效用的癌症生物标志物检测极具吸引力。在患者从最初检测到治疗再到监测的整个过程中,有几个环节DNA甲基化检测可为临床实践提供信息。对手术切除的肿瘤组织进行检测有助于确定治疗耐药指标、预后结果,或对肿瘤进行分子特征分析、分类以及确定肿瘤的组织起源。癌症相关的DNA甲基化变化也能在血液、粪便、尿液和其他生物样本中的游离DNA中准确检测到。此类检测对于开发适用于人群筛查的简单、经济且高度特异的癌症检测方法具有很大潜力,目前已有多个成功转化的实例。循环肿瘤DNA液体活检检测监测癌症的能力还使其能够监测对治疗的反应、检测微小残留病以及作为癌症复发的早期生物标志物。本综述将总结上述应用领域中临床实践中使用的现有DNA甲基化癌症生物标志物,讨论成为合适的DNA甲基化癌症生物标志物的因素,并确定转化过程中的障碍。我们将讨论诸如分析性能和产品与市场匹配度等技术因素,有助于成功进行下游投资的因素(包括地域因素),以及这如何影响知识产权、监管障碍以及市场和医疗保健系统的未来。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99f8/6870840/69065e7c2174/fgene-10-01150-g001.jpg

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