Wang Kendric, Wang Yuzhuo, Collins Colin C
Vancouver Prostate Centre & Department of Urologic Sciences, University of British Columbia, Vancouver, BC V6H 3Z6, Canada.
Asian J Androl. 2013 Nov;15(6):711-2. doi: 10.1038/aja.2013.109. Epub 2013 Aug 26.
Early massively-parallel sequencing studies have revealed the mutational landscape of protein-coding genes in prostate cancer. However, most of these studies have not explored the extensive influence of genomic rearrangement in prostate cancer. In a recent Cell article, Baca and colleagues used whole-genome sequencing to tackle this issue, comprehensively surveying the abundance of genomic rearrangements present in a large cohort of 57 prostate cancers. They characterized a wide-spread phenomenon termed 'chromoplexy', which may drive cancer evolution through the phenomena of punctuated equilibrium by concurrently dysregulating numerous cancer genes across multiple chromosomes. While the causes of this event still require elucidation, this defining discovery undoubtedly offers an important glimpse into the evolutionary process of prostate cancer.
早期的大规模平行测序研究揭示了前列腺癌中蛋白质编码基因的突变图谱。然而,这些研究大多未探究基因组重排对前列腺癌的广泛影响。在最近发表于《细胞》杂志的一篇文章中,巴卡及其同事利用全基因组测序来解决这一问题,全面调查了57例前列腺癌的大型队列中存在的基因组重排丰度。他们描述了一种广泛存在的现象,称为“染色体复杂性”,这种现象可能通过间断平衡现象,同时失调多条染色体上的众多癌症基因,从而推动癌症进化。虽然这一事件的原因仍有待阐明,但这一决定性的发现无疑为前列腺癌的进化过程提供了重要的见解。