DNA甲基化
生物
癌症研究
亚硫酸氢盐测序
表观遗传学
甲基化
计算生物学
DNA
分子生物学
基因
表观遗传学
遗传学
基因表达
作者
Lei Zhao,Xiaohong Wu,Junnian Zheng,Dong Dong
出处
期刊:Oncogene
[Springer Nature]
日期:2021-02-09
卷期号:40 (10): 1884-1895
被引量:50
标识
DOI:10.1038/s41388-021-01657-0
摘要
DNA methylation plays a pivotal role in regulating cellular processes, and altered DNA methylation pattern is a general hallmark of cancer. However, DNA methylome in circulating tumor cells (CTCs) is still a mystery due to the lack of proper analytical techniques. We introduced an efficient workflow, LCM-µWGBS, which can efficiently profile the DNA methylation of microdissected samples. LCM-µWGBS combines the laser capture microdissection (LCM)-based capture method and whole-genome bisulfite sequencing in very small population (µWGBS) to gain insight into the DNA methylation landscape of CTCs. We herein profiled the DNA methylome of CTCs from lung cancer patients. Deriving from a comprehensive analysis of methylome, a unique CTC DNA methylation signature that is distinct from primary lung cancer tissues was identified. Further analysis showed that promoter hypermethylation of epithelial genes is a hallmark of stable epithelial-mesenchymal transition process. Moreover, it has been suggested that CTCs are endowed with a stemness-related feature during dissemination and metastasis. This work constitutes a unique DNA methylation analysis of CTCs at single base-pair resolution, which might facilitate to propose noninvasive DNA methylation biomarkers contributing to clinical diagnosis.
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