Edwin L. Steele Laboratory for Tumour Biology, Massachusetts General Hospital and Harvard Medical School, 100 Blossom Street, Cox 7, Boston, MA 02114, USA.
Nat Rev Clin Oncol. 2015 May;12(5):258-72. doi: 10.1038/nrclinonc.2014.238. Epub 2015 Jan 20.
In cancer, much uncertainty remains regarding the origins of metastatic disease. Models of metastatic progression offer competing views on when dissemination occurs (at an early or late stage of tumour development), whether metastases at different sites arise independently and directly from the primary tumour or give rise to each other, and whether dynamic cell exchange occurs between synchronously growing lesions. Although it is probable that many routes can lead to the establishment of systemic disease, clinical observations suggest that distinct modes of metastasis might prevail in different tumour types. Gaining a more-comprehensive understanding of the evolutionary processes that underlie metastasis is not only relevant from a basic biological perspective, but also has profound clinical implications. The 'tree of life' of metastatic cancer contains answers to many outstanding questions about the development of systemic disease, but has only been reconstructed in a limited number of patients. Here we review available data on the phylogenetic relationships between primary solid tumours and their metastases, and examine to what degree they support different models of metastatic progression. We provide a description of experimental methods for lineage tracing in human cancer, ranging from broad DNA-sequencing approaches to more-targeted techniques, and discuss their respective benefits and caveats. Finally, we propose future research questions in the area of cancer phylogenetics.
在癌症中,转移性疾病的起源仍存在许多不确定性。转移性进展模型提供了关于传播发生时间的相互竞争的观点(在肿瘤发展的早期或晚期),是否不同部位的转移是否独立且直接源自原发性肿瘤,或者是否彼此产生,以及是否在同步生长的病变之间发生动态细胞交换。尽管许多途径可能导致全身性疾病的建立,但临床观察表明,不同的肿瘤类型可能存在不同的转移模式。更全面地了解转移性疾病的进化过程不仅具有基础生物学意义,而且具有深远的临床意义。转移性癌症的“生命之树”包含了许多关于系统性疾病发展的未解决问题的答案,但仅在有限数量的患者中进行了重建。在这里,我们回顾了原发性实体瘤及其转移瘤之间系统发育关系的现有数据,并研究了它们在多大程度上支持不同的转移进展模型。我们提供了用于人类癌症谱系追踪的实验方法的描述,范围从广泛的 DNA 测序方法到更具针对性的技术,并讨论了它们各自的优缺点。最后,我们提出了癌症系统发生学领域的未来研究问题。