表观遗传学
生物
肿瘤异质性
DNA甲基化
染色质
表观遗传学
DNA测序
遗传学
癌症
胎儿游离DNA
基因组学
DNA
癌症研究
生物信息学
计算生物学
基因
基因组
基因表达
胎儿
产前诊断
怀孕
作者
Sally L. George,Claire Lynn,Reda Stankunaite,Debbie Hughes,Carolin M. Sauer,Jane Chalker,Saira Waqar Ahmed,Minou Oostveen,Paula Proszek,Lina Yuan,Ridwan Shaikh,Sabri Jamal,Ama Brew,Jennifer Tall,Tony Rogers,Steven C. Clifford,Josef Vormoor,Janet Shipley,Deborah A. Tweddle,Chris Jones
标识
DOI:10.1158/2159-8290.cd-24-0916
摘要
Abstract We profiled a large heterogenous cohort of matched diagnostic-relapse tumour tissue and paired plasma-derived cell free DNA (cfDNA) from patients with relapsed and progressive solid tumours of childhood. Tissue and cfDNA sequencing results were concordant, with a wider spectrum of mutant alleles and higher degree of intra-tumour heterogeneity captured by the latter, if sufficient circulating tumour-derived DNA (ctDNA) was present. Serial tumour sequencing identified putative drivers of relapse, with alterations in epigenetic drivers being a common feature. In keeping with epigenetic alterations being a common driver of many childhood cancers, fragmentomics analysis of cfDNA identified tumour-specific epigenetic states and transcription factor binding sites accessible in chromatin. This study leverages a large and well-annotated genomic dataset of aggressive childhood malignancies, identifies genomic and epigenetic drivers of childhood cancer relapse, and highlights the power and practicality of cfDNA analysis to capture both intra-tumoural heterogeneity and the epigenetic state of cancer cells.
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