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基于甲基化的液体活检在癌症诊断中的当前挑战

Current Challenges of Methylation-Based Liquid Biopsies in Cancer Diagnostics.

作者信息

Rendek Tomas, Pos Ondrej, Duranova Terezia, Saade Rami, Budis Jaroslav, Repiska Vanda, Szemes Tomas

机构信息

Institute of Medical Biology, Genetics and Clinical Genetics, Faculty of Medicine, Comenius University, 811 08 Bratislava, Slovakia.

Geneton Ltd., 841 04 Bratislava, Slovakia.

出版信息

Cancers (Basel). 2024 May 24;16(11):2001. doi: 10.3390/cancers16112001.

Abstract

In current clinical practice, effective cancer testing and screening paradigms are limited to specific types of cancer, exhibiting varying efficiency, acceptance, and adherence. Cell-free DNA (cfDNA) methylation profiling holds promise in providing information about the presence of malignity regardless of its type and location while leveraging blood-based liquid biopsies as a method to obtain analytical samples. However, technical difficulties, costs and challenges resulting from biological variations, tumor heterogeneity, and exogenous factors persist. This method exploits the mechanisms behind cfDNA release but faces issues like fragmentation, low concentrations, and high background noise. This review explores cfDNA methylation's origins, means of detection, and profiling for cancer diagnostics. The critical evaluation of currently available multi-cancer early detection methods (MCEDs) as well as tests targeting single genes, emphasizing their potential and limits to refine strategies for early cancer detection, are explained. The current methodology limitations, workflows, comparisons of clinically approved liquid biopsy-based methylation tests for cancer, their utilization in companion diagnostics as well as the biological limitations of the epigenetics approach are discussed, aiming to help healthcare providers as well as researchers to orient themselves in this increasingly complex and evolving field of diagnostics.

摘要

在当前的临床实践中,有效的癌症检测和筛查模式仅限于特定类型的癌症,其效率、接受度和依从性各不相同。游离DNA(cfDNA)甲基化分析有望提供有关恶性肿瘤存在与否的信息,而不论其类型和位置如何,同时利用基于血液的液体活检作为获取分析样本的方法。然而,技术难题、成本以及生物变异、肿瘤异质性和外部因素带来的挑战依然存在。这种方法利用了cfDNA释放背后的机制,但面临着片段化、浓度低和背景噪音高等问题。本综述探讨了cfDNA甲基化的起源、检测方法以及用于癌症诊断的分析。解释了对当前可用的多癌早期检测方法(MCED)以及针对单个基因的检测进行的批判性评估,强调了它们在完善早期癌症检测策略方面的潜力和局限性。讨论了当前的方法局限性、工作流程、临床上批准的基于液体活检的癌症甲基化检测的比较、它们在伴随诊断中的应用以及表观遗传学方法的生物学局限性,旨在帮助医疗保健提供者和研究人员在这个日益复杂和不断发展的诊断领域中找准方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47e4/11171112/939344651242/cancers-16-02001-g001.jpg

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