1] Cancer Vaccine Center, Dana-Farber Cancer Institute, Boston, MA, USA [2] Broad Institute, Cambridge, MA, USA [3] Department of Hematology, Yale Cancer Center, New Haven, CT, USA [4] Université Paris Diderot, Paris, France.
Broad Institute, Cambridge, MA, USA.
Leukemia. 2014 Jan;28(1):34-43. doi: 10.1038/leu.2013.248. Epub 2013 Aug 27.
The ability of cancer to evolve and adapt is a principal challenge to therapy in general and to the paradigm of targeted therapy in particular. This ability is fueled by the co-existence of multiple, genetically heterogeneous subpopulations within the cancer cell population. Increasing evidence has supported the idea that these subpopulations are selected in a Darwinian fashion, by which the genetic landscape of the tumor is continuously reshaped. Massively parallel sequencing has enabled a recent surge in our ability to study this process, adding to previous efforts using cytogenetic methods and targeted sequencing. Altogether, these studies reveal the complex evolutionary trajectories occurring across individual hematological malignancies. They also suggest that while clonal evolution may contribute to resistance to therapy, treatment may also hasten the evolutionary process. New insights into this process challenge us to understand the impact of treatment on clonal evolution and inspire the development of novel prognostic and therapeutic strategies.
癌症进化和适应的能力是治疗的主要挑战,尤其是针对靶向治疗的范式。这种能力是由癌症细胞群体中多种遗传异质性亚群的共存所驱动的。越来越多的证据支持这样一种观点,即这些亚群是通过达尔文式的选择而被选择出来的,通过这种选择,肿瘤的遗传景观不断被重塑。大规模平行测序使我们最近能够增强研究这一过程的能力,这增加了以前使用细胞遗传学方法和靶向测序的努力。总的来说,这些研究揭示了个体血液恶性肿瘤中发生的复杂进化轨迹。它们还表明,虽然克隆进化可能导致对治疗的耐药性,但治疗也可能加速进化过程。对这一过程的新见解挑战我们去理解治疗对克隆进化的影响,并激发新的预后和治疗策略的发展。