Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Genes Chromosomes Cancer. 2023 Sep;62(9):501-509. doi: 10.1002/gcc.23141. Epub 2023 Mar 30.
The role of cancer relevant translocations in tumorigenesis has been historically hampered by the lack of faithful in vitro and in vivo models. The development of the latest genome editing tools (e.g., CRISPR-Cas9) allowed modeling of various chromosomal translocations with different effects on proliferation and transformation capacity depending on the cell line used and secondary genetic alterations. The cellular context is particularly relevant in the case of oncogenic fusions expressed in sarcomas whose histogenesis remain uncertain. Moreover, recent studies have emphasized the increased frequency of gene fusion promiscuity across different mesenchymal tumor entities, which are clinicopathologically unrelated. This review provides a summary of different strategies utilized to generate cancer models with a focus on fusion-driven mesenchymal neoplasia.
癌症相关易位在肿瘤发生中的作用一直受到缺乏忠实的体外和体内模型的阻碍。最新基因组编辑工具(例如,CRISPR-Cas9)的发展允许对各种染色体易位进行建模,其对增殖和转化能力的影响取决于所使用的细胞系和继发性遗传改变。在肉瘤中表达的致癌融合的情况下,细胞环境尤其重要,肉瘤的组织发生仍然不确定。此外,最近的研究强调了不同间充质肿瘤实体中基因融合混杂的频率增加,这些实体在临床病理上没有关系。这篇综述提供了总结不同策略的概要,这些策略用于生成以融合驱动的间充质肿瘤为重点的癌症模型。