Wellcome Trust Sanger Institute, Hinxton, Cambridge, UK.
Science. 2011 Mar 25;331(6024):1553-8. doi: 10.1126/science.1204040.
The description and interpretation of genomic abnormalities in cancer cells have been at the heart of cancer research for more than a century. With exhaustive sequencing of cancer genomes across a wide range of human tumors well under way, we are now entering the end game of this mission. In the forthcoming decade, essentially complete catalogs of somatic mutations will be generated for tens of thousands of human cancers. Here, I provide an overview of what these efforts have revealed to date about the origin and behavioral features of cancer cells and how this genomic information is being exploited to improve diagnosis and therapy of the disease.
一个多世纪以来,对癌细胞中基因组异常的描述和阐释一直是癌症研究的核心。对广泛人类肿瘤的癌症基因组进行详尽测序的工作已在进行中,我们现在正进入这一任务的最后阶段。在即将到来的十年中,将为数以万计的人类癌症生成基本上完整的体细胞突变目录。在这里,我概述了这些研究迄今为止揭示的关于癌细胞的起源和行为特征的信息,以及如何利用这些基因组信息来改善疾病的诊断和治疗。