The Jackson Laboratory for Genomic Medicine, Farmington, CT, USA.
Department of Paediatric Oncology/Hematology, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Nat Rev Genet. 2022 Dec;23(12):760-771. doi: 10.1038/s41576-022-00521-5. Epub 2022 Aug 11.
Extrachromosomal DNA (ecDNA) amplification is an important driver alteration in cancer. It has been observed in most cancer types and is associated with worse patient outcome. The functional impact of ecDNA has been linked to its unique properties, such as its circular structure that is associated with altered chromatinization and epigenetic regulatory landscape, as well as its ability to randomly segregate during cell division, which fuels intercellular copy number heterogeneity. Recent investigations suggest that ecDNA is structurally more complex than previously anticipated and that it localizes to specialized nuclear bodies (hubs) and can act in trans as an enhancer for genes on other ecDNAs or chromosomes. In this Review, we synthesize what is currently known about how ecDNA is generated and how its genetic and epigenetic architecture affects proto-oncogene deregulation in cancer. We discuss how recently identified ecDNA functions may impact oncogenesis but also serve as new therapeutic vulnerabilities in cancer.
染色体外 DNA(ecDNA)扩增是癌症中一个重要的驱动改变。它在大多数癌症类型中都有观察到,并与患者预后较差相关。ecDNA 的功能影响与其独特的性质有关,例如其环状结构与染色质重塑和表观遗传调控景观的改变有关,以及其在细胞分裂过程中随机分离的能力,这促进了细胞间拷贝数异质性。最近的研究表明,ecDNA 的结构比以前预期的更为复杂,它定位于专门的核体(中心),并且可以作为其他 ecDNA 或染色体上基因的增强子起作用。在这篇综述中,我们综合了目前已知的关于 ecDNA 是如何产生的,以及其遗传和表观遗传结构如何影响癌症中原癌基因失调的信息。我们讨论了最近发现的 ecDNA 功能可能如何影响致癌作用,但也作为癌症中的新的治疗弱点。