Division of Cell Biology, Oncode Institute, The Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX, Amsterdam, The Netherlands.
Center for Molecular Medicine, University Medical Center Utrecht, Utrecht University, Universiteitsweg, 100, 3584, CG Utrecht, The Netherlands.
Chromosoma. 2022 Sep;131(3):107-125. doi: 10.1007/s00412-022-00773-4. Epub 2022 Apr 30.
Advances in genome sequencing have revealed a type of extrachromosomal DNA, historically named double minutes (also referred to as ecDNA), to be common in a wide range of cancer types, but not in healthy tissues. These cancer-associated circular DNA molecules contain one or a few genes that are amplified when double minutes accumulate. Double minutes harbor oncogenes or drug resistance genes that contribute to tumor aggressiveness through copy number amplification in combination with favorable epigenetic properties. Unequal distribution of double minutes over daughter cells contributes to intratumoral heterogeneity, thereby increasing tumor adaptability. In this review, we discuss various models delineating the mechanism of generation of double minutes. Furthermore, we highlight how double minutes are maintained, how they evolve, and discuss possible mechanisms driving their elimination.
基因组测序的进展揭示了一种染色体外 DNA 类型,历史上称为双微体(也称为 ecDNA),在广泛的癌症类型中很常见,但在健康组织中不存在。这些与癌症相关的环状 DNA 分子包含一个或几个基因,当双微体积累时这些基因被扩增。双微体含有癌基因或耐药基因,通过与有利的表观遗传特性相结合的拷贝数扩增,促进肿瘤侵袭性。双微体在子细胞中的不均匀分布导致肿瘤内异质性增加,从而提高肿瘤的适应性。在这篇综述中,我们讨论了各种模型来描述双微体产生的机制。此外,我们还强调了双微体是如何维持的,它们是如何进化的,并讨论了驱动它们消除的可能机制。