Barber Louise J, Davies Matthew N, Gerlinger Marco
Translational Oncogenomics Laboratory, Centre for Evolution and Cancer, Division of Molecular Pathology, The Institute of Cancer Research, 237 Fulham Road, London SW3 6JB, UK.
Translational Oncogenomics Laboratory, Centre for Evolution and Cancer, Division of Molecular Pathology, The Institute of Cancer Research, 237 Fulham Road, London SW3 6JB, UK; Gastrointestinal Cancer Unit, The Royal Marsden Hospital NHS Foundation Trust, Fulham Road, London SW3 6JJ, UK.
Curr Opin Genet Dev. 2015 Feb;30:1-6. doi: 10.1016/j.gde.2014.12.001. Epub 2014 Dec 31.
Intratumour heterogeneity complicates biomarker discovery and treatment personalization, and pervasive cancer evolution is a key mechanism leading to therapy failure and patient death. Thus, understanding subclonal heterogeneity architectures and cancer evolution processes is critical for the development of effective therapeutic approaches which can control or thwart cancer evolutionary plasticity. Current insights into heterogeneity are mainly limited to the macroheterogeneity level, established by cancer subclones that have undergone significant clonal expansion. Novel single cell sequencing and blood-based subclonal tracking technologies are enabling detailed insights into microheterogeneity and the dynamics of clonal evolution. We assess how this starts to delineate the rules governing cancer evolution and novel angles for more effective therapeutic intervention.
肿瘤内异质性使生物标志物发现和治疗个性化变得复杂,而普遍存在的癌症进化是导致治疗失败和患者死亡的关键机制。因此,了解亚克隆异质性结构和癌症进化过程对于开发能够控制或阻止癌症进化可塑性的有效治疗方法至关重要。目前对异质性的认识主要局限于宏观异质性水平,这是由经历了显著克隆扩增的癌症亚克隆所建立的。新型单细胞测序和基于血液的亚克隆追踪技术能够深入了解微异质性和克隆进化动态。我们评估这如何开始描绘出癌症进化的规则以及更有效治疗干预的新角度。