白血病
表观基因组
生物
表观遗传学
癌症的体细胞进化
免疫学
癌症研究
遗传学
DNA甲基化
癌症
基因
基因表达
作者
Monika M. Toma,Tomasz Skórski
出处
期刊:Leukemia
[Springer Nature]
日期:2024-09-02
标识
DOI:10.1038/s41375-024-02369-6
摘要
Abstract Leukemia, although most likely starts as a monoclonal genetic/epigenetic anomaly, is a polyclonal disease at manifestation. This polyclonal nature results from ongoing evolutionary changes in the genome/epigenome of leukemia cells to promote their survival and proliferation advantages. We discuss here how genetic and/or epigenetic aberrations alter intracellular microenvironment in individual leukemia clones and how extracellular microenvironment selects the best fitted clones. This dynamic polyclonal composition of leukemia makes designing an effective therapy a challenging task especially because individual leukemia clones often display substantial differences in response to treatment. Here, we discuss novel therapeutic approach employing single cell multiomics to identify and eradicate all individual clones in a patient.
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