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临床癌症诊疗中新兴的循环肿瘤DNA检测策略。

Emerging ctDNA detection strategies in clinical cancer theranostics.

作者信息

Yi Kexin, Wang Xiaoju, Filippov Sergey K, Zhang Hongbo

机构信息

Pharmaceutical Sciences Laboratory Åbo Akademi University Turku Finland.

DWI-Leibniz Institute for Interactive Materials e. V. Aachen Germany.

出版信息

Smart Med. 2023 Nov 13;2(4):e20230031. doi: 10.1002/SMMD.20230031. eCollection 2023 Nov.

Abstract

Circulating tumor DNA (ctDNA) is naked DNA molecules shed from the tumor cells into the peripheral blood circulation. They contain tumor-specific gene mutations and other valuable information. ctDNA is considered to be one of the most significant analytes in liquid biopsies. Over the past decades, numerous researchers have developed various detection strategies to perform quantitative or qualitative ctDNA analysis, including PCR-based detection and sequencing-based detection. More and more studies have illustrated the great value of ctDNA as a biomarker in the diagnosis, prognosis and heterogeneity of tumor. In this review, we first outlined the development of digital PCR (dPCR)-based and next generation sequencing (NGS)-based ctDNA detection systems. Besides, we presented the introduction of the emerging ctDNA analysis strategies based on various biosensors, such as electrochemical biosensors, fluorescent biosensors, surface plasmon resonance and Raman spectroscopy, as well as their applications in the field of biomedicine. Finally, we summarized the essentials of the preceding discussions, and the existing challenges and prospects for the future are also involved.

摘要

循环肿瘤DNA(ctDNA)是从肿瘤细胞释放到外周血液循环中的无细胞DNA分子。它们包含肿瘤特异性基因突变和其他有价值的信息。ctDNA被认为是液体活检中最重要的分析物之一。在过去几十年中,众多研究人员开发了各种检测策略来进行ctDNA的定量或定性分析,包括基于PCR的检测和基于测序的检测。越来越多的研究表明ctDNA作为生物标志物在肿瘤的诊断、预后和异质性方面具有巨大价值。在本综述中,我们首先概述了基于数字PCR(dPCR)和基于下一代测序(NGS)的ctDNA检测系统的发展。此外,我们介绍了基于各种生物传感器(如电化学生物传感器、荧光生物传感器、表面等离子体共振和拉曼光谱)的新兴ctDNA分析策略,以及它们在生物医学领域的应用。最后,我们总结了上述讨论的要点,并涉及了当前存在的挑战和未来的前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c71c/11235813/ee313bbda020/SMMD-2-e20230031-g007.jpg

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