Single-cell epigenomics in cancer: charting a course to clinical impact

被引:7
|
作者
Bond, Danielle R. [1 ]
Uddipto, Kumar [1 ]
Enjeti, Anoop K. [2 ,3 ,4 ]
Lee, Heather J. [1 ]
机构
[1] Univ Newcastle, Fac Hlth & Med, Sch Biomed Sci & Pharm, Callaghan, NSW 2308, Australia
[2] Calvary Mater Newcastle, Dept Haematol, Waratah, NSW 2298, Australia
[3] Univ Newcastle, Fac Hlth & Med, Sch Med & Publ Hlth, Callaghan, NSW 2308, Australia
[4] NSW Hlth Pathol Hunter, New Lambton Hts, NSW 2305, Australia
基金
澳大利亚研究理事会; 英国医学研究理事会;
关键词
cancer; epigenetics; intra-tumoral heterogeneity; sequencing; single-cell analysis; MINIMAL RESIDUAL DISEASE; TUMOR-SUPPRESSOR GENES; DNA METHYLATION; EPIGENETIC MODIFICATIONS; RNA-SEQ; PROMOTER HYPERMETHYLATION; BREAST-CANCER; STEM-CELLS; CHROMATIN; EVOLUTION;
D O I
10.2217/epi-2020-0046
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Cancer is a disease of global epigenetic dysregulation. Mutations in epigenetic regulators are common events in multiple cancer types and epigenetic therapies are emerging as a treatment option in several malignancies. A major challenge for the clinical management of cancer is the heterogeneous nature of this disease. Cancers are composed of numerous cell types and evolve over time. This heterogeneity confounds decisions regarding treatment and promotes disease relapse. The emergence of single-cell epigenomic technologies has introduced the exciting possibility of linking genetic and transcriptional heterogeneity in the context of cancer biology. The next challenge is to leverage these tools for improved patient outcomes. Here we consider how single-cell epigenomic technologies may address the current challenges faced by cancer clinicians.
引用
收藏
页码:1139 / 1151
页数:14
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