Cancer Genomics, Peter MacCallum Cancer Centre, East Melbourne, VIC 3002, Australia; Sir Peter MacCallum Department of Oncology, University of Melbourne, VIC 3010, Australia; Department of Pathology, University of Melbourne, VIC 3010, Australia.
Chromosome Research, Murdoch Childrens Research Institute, and Department of Paediatrics, Royal Children's Hospital, University of Melbourne, Parkville, VIC 3052, Australia.
Cancer Cell. 2014 Nov 10;26(5):653-67. doi: 10.1016/j.ccell.2014.09.010.
We isolated and analyzed, at single-nucleotide resolution, cancer-associated neochromosomes from well- and/or dedifferentiated liposarcomas. Neochromosomes, which can exceed 600 Mb in size, initially arise as circular structures following chromothripsis involving chromosome 12. The core of the neochromosome is amplified, rearranged, and corroded through hundreds of breakage-fusion-bridge cycles. Under selective pressure, amplified oncogenes are overexpressed, while coamplified passenger genes may be silenced epigenetically. New material may be captured during punctuated chromothriptic events. Centromeric corrosion leads to crisis, which is resolved through neocentromere formation or native centromere capture. Finally, amplification terminates, and the neochromosome core is stabilized in linear form by telomere capture. This study investigates the dynamic mutational processes underlying the life history of a special form of cancer mutation.
我们从分化良好和/或去分化脂肪肉瘤中分离和分析了单核苷酸分辨率的癌症相关的新染色体。新染色体的大小可以超过 600Mb,最初是在涉及 12 号染色体的染色体重排后作为环状结构出现的。新染色体的核心通过数百个断裂-融合-桥循环进行扩增、重排和侵蚀。在选择压力下,扩增的癌基因过表达,而共扩增的乘客基因可能被表观遗传沉默。在间断的染色体重排事件中可能会捕获新的物质。着丝粒侵蚀导致危机,通过新着丝粒形成或天然着丝粒捕获来解决。最后,扩增终止,新染色体核心通过端粒捕获稳定在线性形式。本研究调查了一种特殊形式的癌症突变的生命史背后的动态突变过程。