Shah Dinakshi, Lamarca Angela, Valle Juan W, McNamara Mairéad G
Department of Medical Oncology, The Christie NHS Foundation Trust, Manchester M20 4BX, UK.
Division of Cancer Sciences, University of Manchester, Manchester M13 9PL, UK.
J Clin Med. 2021 Jan 21;10(3):403. doi: 10.3390/jcm10030403.
Tumour tissue as a source for molecular profiling and for in vivo models has limitations (e.g., difficult access, limited availability, single time point, potential heterogeneity between primary and metastatic sites). Conversely, liquid biopsies provide an easily accessible approach, enabling timely and longitudinal interrogation of the tumour molecular makeup, with increased ability to capture spatial and temporal intra-tumour heterogeneity compared to tumour tissue. Blood-borne biomarker assays (e.g., circulating tumour cells (CTCs), circulating free/tumour DNA (cf/ctDNA)) pose unique opportunities for aiding in the molecular characterisation and phenotypic subtyping of neuroendocrine neoplasms and will be discussed in this article.
肿瘤组织作为分子谱分析和体内模型的来源存在局限性(例如,获取困难、可用性有限、单一时间点、原发部位和转移部位之间可能存在异质性)。相反,液体活检提供了一种易于获取的方法,能够及时且纵向地探究肿瘤分子构成,与肿瘤组织相比,其捕获肿瘤内空间和时间异质性的能力更强。血源生物标志物检测(例如,循环肿瘤细胞(CTC)、循环游离/肿瘤DNA(cf/ctDNA))为辅助神经内分泌肿瘤的分子特征分析和表型亚型划分带来了独特机遇,本文将对此进行讨论。