Graduate School of Integrated Sciences for Life, Hiroshima University, 1-7-1 Kagamiyama, Higashi-Hiroshima 739-8521, Hiroshima, Japan.
Genes (Basel). 2021 Sep 28;12(10):1533. doi: 10.3390/genes12101533.
Oncogene amplification is closely linked to the pathogenesis of a broad spectrum of human malignant tumors. The amplified genes localize either to the extrachromosomal circular DNA, which has been referred to as cytogenetically visible double minutes (DMs), or submicroscopic episome, or to the chromosomal homogeneously staining region (HSR). The extrachromosomal circle from a chromosome arm can initiate gene amplification, resulting in the formation of DMs or HSR, if it had a sequence element required for replication initiation (the replication initiation region/matrix attachment region; the IR/MAR), under a genetic background that permits gene amplification. In this article, the nature, intracellular behavior, generation, and contribution to cancer genome plasticity of such extrachromosomal circles are summarized and discussed by reviewing recent articles on these topics. Such studies are critical in the understanding and treating human cancer, and also for the production of recombinant proteins such as biopharmaceuticals by increasing the recombinant genes in the cells.
癌基因扩增与广泛的人类恶性肿瘤的发病机制密切相关。扩增的基因定位于染色体外的环状 DNA,即细胞遗传学可见的双微体(DMs),或亚显微的附加体,或染色体均质染色区(HSR)。如果染色体臂上的环状 DNA 具有复制起始所需的序列元件(复制起始区/基质附着区;IR/MAR),并且存在允许基因扩增的遗传背景,则它可以启动基因扩增,导致 DMs 或 HSR 的形成。在本文中,通过回顾关于这些主题的最新文章,总结和讨论了这种染色体外环状 DNA 的性质、细胞内行为、产生以及对癌症基因组可塑性的贡献。这些研究对于理解和治疗人类癌症以及通过增加细胞中的重组基因来生产生物制药等重组蛋白至关重要。