Institut Curie, PSL Research University, Paris, France.
INSERM U900, Paris, France.
Methods Mol Biol. 2021;2226:303-333. doi: 10.1007/978-1-0716-1020-6_23.
Ewing sarcoma (EwS) is a highly aggressive pediatric bone cancer that is defined by a somatic fusion between the EWSR1 gene and an ETS family member, most frequently the FLI1 gene, leading to expression of a chimeric transcription factor EWSR1-FLI1. Otherwise, EwS is one of the most genetically stable cancers. The situation when the major cancer driver is well known looks like a unique opportunity for applying the systems biology approach in order to understand the EwS mechanisms as well as to uncover some general mechanistic principles of carcinogenesis. A number of studies have been performed revealing the direct and indirect effects of EWSR1-FLI1 on multiple aspects of cellular life. Nevertheless, the emerging picture of the oncogene action appears to be highly complex and systemic, with multiple reciprocal influences between the immediate consequences of the driver mutation and intracellular and intercellular molecular mechanisms, including regulation of transcription, epigenome, and tumoral microenvironment. In this chapter, we present an overview of existing molecular profiling resources available for EwS tumors and cell lines and provide an online comprehensive catalogue of publicly available omics and other datasets. We further highlight the systems biology studies of EwS, involving mathematical modeling of networks and integration of molecular data. We conclude that despite the seeming simplicity, a lot has yet to be understood on the systems-wide mechanisms connecting the driver mutation and the major cellular phenotypes of this pediatric cancer. Overall, this chapter can serve as a guide for a systems biology researcher to start working on EwS.
尤因肉瘤 (EwS) 是一种高度侵袭性的儿科骨癌,其特征是 EWSR1 基因与 ETS 家族成员(最常见的是 FLI1 基因)之间发生体细胞融合,导致嵌合转录因子 EWSR1-FLI1 的表达。否则,EwS 是遗传上最稳定的癌症之一。在主要致癌驱动因素已知的情况下,这似乎是应用系统生物学方法的独特机会,以便了解 EwS 机制并揭示致癌发生的一些一般机制原则。已经进行了多项研究,揭示了 EWSR1-FLI1 对细胞生命多个方面的直接和间接影响。然而,致癌基因作用的新兴图景似乎非常复杂和系统,驱动突变的直接后果与细胞内和细胞间的分子机制之间存在多种相互影响,包括转录、表观基因组和肿瘤微环境的调节。在本章中,我们介绍了现有的用于 EwS 肿瘤和细胞系的分子图谱资源概述,并提供了公开可用的组学和其他数据集的在线综合目录。我们进一步强调了 EwS 的系统生物学研究,涉及网络的数学建模和分子数据的整合。我们得出的结论是,尽管表面上看起来很简单,但对于连接驱动突变和这种儿科癌症的主要细胞表型的系统范围机制,仍有很多需要理解。总的来说,本章可以作为系统生物学研究人员开始研究 EwS 的指南。