Extrachromosomal DNA in cancer

被引:0
作者
Xiaowei Yan
Paul Mischel
Howard Chang
机构
[1] Stanford University,Department of Dermatology
[2] Stanford University,Center for Personal Dynamic Regulomes
[3] Stanford University School of Medicine,Department of Pathology
[4] Stanford University,Sarafan ChEM
[5] Stanford University,H
来源
Nature Reviews Cancer | 2024年 / 24卷
关键词
D O I
暂无
中图分类号
学科分类号
摘要
Extrachromosomal DNA (ecDNA) has recently been recognized as a major contributor to cancer pathogenesis that is identified in most cancer types and is associated with poor outcomes. When it was discovered over 60 years ago, ecDNA was considered to be rare, and its impact on tumour biology was not well understood. The application of modern imaging and computational techniques has yielded powerful new insights into the importance of ecDNA in cancer. The non-chromosomal inheritance of ecDNA during cell division results in high oncogene copy number, intra-tumoural genetic heterogeneity and rapid tumour evolution that contributes to treatment resistance and shorter patient survival. In addition, the circular architecture of ecDNA results in altered patterns of gene regulation that drive elevated oncogene expression, potentially enabling the remodelling of tumour genomes. The generation of clusters of ecDNAs, termed ecDNA hubs, results in interactions between enhancers and promoters in trans, yielding a new paradigm in oncogenic transcription. In this Review, we highlight the rapid advancements in ecDNA research, providing new insights into ecDNA biogenesis, maintenance and transcription and its role in promoting tumour heterogeneity. To conclude, we delve into a set of unanswered questions whose answers will pave the way for the development of ecDNA targeted therapeutic approaches.
引用
收藏
页码:261 / 273
页数:12
相关论文
共 223 条
  • [51] Lin CC(2021)Chromothripsis drives the evolution of gene amplification in cancer Nature 591 880-9145
  • [52] Varmus HE(2023)Single‐cell third‐generation sequencing‐based multi‐omics uncovers gene expression changes governed by ecDNA and structural variants in cancer cells Clin. Transl. Med. 13 11368-172
  • [53] Bishop JM(2013)Double minute chromosomes in glioblastoma multiforme are revealed by precise reconstruction of oncogenic amplicons Cancer Res. 73 107-929
  • [54] Nathanson DA(2019)Exploring the landscape of focal amplifications in cancer using AmpliconArchitect Nat. Commun. 10 2152-289
  • [55] Hung KL(2022)Mapping clustered mutations in cancer reveals APOBEC3 mutagenesis of ecDNA Nature 602 9131-1247
  • [56] Mischel PS(2023)Blocking genomic instability prevents acquired resistance to MAPK inhibitor therapy in melanoma Cancer Discov. 13 170-40
  • [57] Chang HY(2023)Parallel sequencing of extrachromosomal circular DNAs and transcriptomes in single cancer cells Nat. Genet. 55 919-715
  • [58] Li Z(2004)Molecular structure of double-minute chromosomes bearing amplified copies of the epidermal growth factor receptor gene in gliomas Proc. Natl Acad. Sci. USA 101 gky767-71
  • [59] Wang B(2006)Translocation–excision–deletion–amplification mechanism leading to nonsyntenic coamplification of MYC and ATBF1 Genes Chromosom. Cancer 45 276-1685
  • [60] Liang H(2018)MYC-containing amplicons in acute myeloid leukemia: genomic structures, evolution, and transcriptional consequences Leukemia 32 1235-36