Cancer, Ageing and Somatic Mutation, Wellcome Sanger Institute, Hinxton, Cambridgeshire CB10 1SA, UK.
Cancer, Ageing and Somatic Mutation, Wellcome Sanger Institute, Hinxton, Cambridgeshire CB10 1SA, UK; Department of Cellular and Molecular Medicine and Department of Bioengineering, Moores Cancer Center, University of California, San Diego, La Jolla, CA 92093, USA.
Cell. 2019 Mar 7;176(6):1282-1294.e20. doi: 10.1016/j.cell.2019.02.012.
Multiple signatures of somatic mutations have been identified in cancer genomes. Exome sequences of 1,001 human cancer cell lines and 577 xenografts revealed most common mutational signatures, indicating past activity of the underlying processes, usually in appropriate cancer types. To investigate ongoing patterns of mutational-signature generation, cell lines were cultured for extended periods and subsequently DNA sequenced. Signatures of discontinued exposures, including tobacco smoke and ultraviolet light, were not generated in vitro. Signatures of normal and defective DNA repair and replication continued to be generated at roughly stable mutation rates. Signatures of APOBEC cytidine deaminase DNA-editing exhibited substantial fluctuations in mutation rate over time with episodic bursts of mutations. The initiating factors for the bursts are unclear, although retrotransposon mobilization may contribute. The examined cell lines constitute a resource of live experimental models of mutational processes, which potentially retain patterns of activity and regulation operative in primary human cancers.
在癌症基因组中已经鉴定出多种体细胞突变的特征。对 1001 个人类癌细胞系和 577 个异种移植物的外显子组序列进行分析,揭示了最常见的突变特征,表明潜在过程的过去活性,通常在适当的癌症类型中。为了研究突变特征生成的持续模式,对细胞系进行了长时间的培养,然后对其进行 DNA 测序。在体外不会产生已停止暴露(包括烟草烟雾和紫外线)的特征。正常和有缺陷的 DNA 修复和复制的特征仍以大致稳定的突变率继续产生。APOBEC 胞嘧啶脱氨酶 DNA 编辑的特征在突变率上随时间有明显波动,有突变爆发的时期。爆发的起始因素尚不清楚,尽管逆转录转座子的动员可能会有贡献。所检查的细胞系构成了突变过程的活体实验模型资源,这些模型可能保留了原发性人类癌症中起作用和调节的模式。