染色质
蒽环类
CTCF公司
生物
计算生物学
表观遗传学
DNA
癌症研究
遗传学
癌症
基因
DNA甲基化
增强子
转录因子
乳腺癌
基因表达
作者
Minkang Tan,S. N. Sun,Yuchen Liu,Andrea A. Perreault,Douglas H. Phanstiel,Liping Dou,Baoxu Pang
标识
DOI:10.1073/pnas.2500704122
摘要
The chromatin is folded into three-dimensional (3D) structures, and aberrant 3D chromatin folding has been implicated in cancer. We performed ATAC-seq and TOP2A ChIP-seq to assess the potential effects of various anthracycline drugs on the chromatin architecture. We found that specific anthracycline variants selectively disrupt chromatin looping anchors by interfering with CTCF binding, suggesting an additional therapeutic mechanism of anthracycline drugs targeting the 3D genome. Hi-C experiments in K562 cells treated with anthracycline drugs revealed widespread disruption of 3D chromatin organization, including altered long-range regulation at the Myc locus. Furthermore, AML patients treated with anthracycline drugs exhibited changes in chromatin structures near possible looping anchors, which were associated with distinct clinical outcomes. Together, our findings indicate that anthracycline drugs function as potent and selective epigenomic modulators, with the capacity to further target the 3D genome to exert anticancer effects, highlighting their potential for personalized therapy in tumors with aberrant 3D chromatin architecture.
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