Stewart Caitlin M, Tsui Dana W Y
Marie-José and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, Box 20, New York, NY 10065, USA; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Marie-José and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, Box 20, New York, NY 10065, USA; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Cancer Genet. 2018 Dec;228-229:169-179. doi: 10.1016/j.cancergen.2018.02.005. Epub 2018 Mar 11.
Cell-free DNA (cfDNA) was first identified in human plasma in 1948 and is thought to be released from cells throughout the body into the circulatory system. In cancer, a portion of the cfDNA originates from tumour cells, referred to as circulating-tumour DNA (ctDNA), and can contain mutations corresponding to the patient's tumour, for instance specific TP53 alleles. Profiling of cfDNA has recently become an area of increasing clinical relevance in oncology, in particular due to advances in the sensitivity of molecular biology techniques and development of next generation sequencing technologies, as this allows tumour mutations to be identified and tracked non-invasively. This has opened up new possibilities for monitoring tumour evolution and acquisition of resistance, as well as for guiding treatment decisions when tumour biopsy tissue is insufficient or unavailable. In this review, we will discuss the biology of cell-free nucleic acids, methods of analysis, and the potential clinical uses of these techniques, as well as the on-going clinical development of ctDNA assays.
游离DNA(cfDNA)于1948年首次在人体血浆中被发现,被认为是从全身细胞释放到循环系统中的。在癌症中,一部分cfDNA源自肿瘤细胞,称为循环肿瘤DNA(ctDNA),并且可能包含与患者肿瘤相对应的突变,例如特定的TP53等位基因。近年来,cfDNA分析在肿瘤学领域的临床相关性日益增加,这尤其得益于分子生物学技术灵敏度的提高和新一代测序技术的发展,因为这使得肿瘤突变能够被非侵入性地识别和追踪。这为监测肿瘤演变和耐药性的获得开辟了新的可能性,也为在肿瘤活检组织不足或无法获取时指导治疗决策提供了可能。在本综述中,我们将讨论游离核酸的生物学特性、分析方法、这些技术的潜在临床应用,以及ctDNA检测的正在进行的临床开发情况。