Yale School of Medicine, New Haven, Connecticut.
NeuroTexas Institute, St. David's Medical Center, Austin, Texas. Center for Systems and Synthetic Biology, University of Texas, Austin, Texas. Fresh Pond Research Institute, Cambridge, Massachusetts.
Cancer Res. 2015 Oct 1;75(19):4021-5. doi: 10.1158/0008-5472.CAN-15-1889. Epub 2015 Aug 10.
Determining the evolutionary history of metastases is a key problem in cancer biology. Several recent studies have presented inferences regarding the origin of metastases based on phylogenies of cancer lineages. Many of these studies have concluded that the observed monophyly of metastatic subclones favored metastasis-to-metastasis spread ("a metastatic cascade" rather than parallel metastases from the primary tumor). In this article, we argue that identifying a monophyletic clade of metastatic subclones does not provide sufficient evidence to unequivocally establish a history of metastatic cascades. In the absence of a complete phylogeny of the subclones within the primary tumor, a scenario of parallel metastatic events from the primary tumor is an equally plausible interpretation. Future phylogenetic studies on the origin of metastases should obtain a complete phylogeny of subclones within the primary tumor. This complete phylogeny may be obtainable by ultra-deep sequencing and phasing of large sections or by targeted sequencing of many small, spatially heterogeneous sections, followed by phylogenetic reconstruction using well-established molecular evolutionary models. In addition to resolving the evolutionary history of metastases, a complete phylogeny of subclones within the primary tumor facilitates the identification of driver mutations by application of phylogeny-based tests of natural selection.
确定转移的进化历史是癌症生物学中的一个关键问题。最近的几项研究基于癌症谱系的系统发育提出了关于转移起源的推断。其中许多研究得出结论,观察到转移亚克隆的单系性支持转移-转移传播(“转移级联”而不是来自原发性肿瘤的平行转移)。在本文中,我们认为,确定转移亚克隆的单系分支并不能提供确凿的证据来明确建立转移级联的历史。在没有原发性肿瘤内亚克隆完整系统发育的情况下,来自原发性肿瘤的平行转移事件的情况同样是一个合理的解释。未来关于转移起源的系统发育研究应该获得原发性肿瘤内亚克隆的完整系统发育。通过对大段进行超深度测序和定相,或对许多小的、空间异质的段进行靶向测序,然后使用成熟的分子进化模型进行系统发育重建,就可以获得完整的系统发育。除了解决转移的进化历史外,原发性肿瘤内亚克隆的完整系统发育还通过应用基于系统发育的自然选择测试来识别驱动突变提供了便利。