Department of Genetics, Stanford University School of Medicine, Stanford, CA, USA.
Department of Biology, Stanford University, Stanford, CA, USA.
Nat Genet. 2018 Apr;50(4):483-486. doi: 10.1038/s41588-018-0083-2. Epub 2018 Apr 2.
The functional impact of most genomic alterations found in cancer, alone or in combination, remains largely unknown. Here we integrate tumor barcoding, CRISPR/Cas9-mediated genome editing and ultra-deep barcode sequencing to interrogate pairwise combinations of tumor suppressor alterations in autochthonous mouse models of human lung adenocarcinoma. We map the tumor suppressive effects of 31 common lung adenocarcinoma genotypes and identify a landscape of context dependence and differential effect strengths.
大多数在癌症中发现的基因组改变的功能影响,无论是单独存在还是组合存在,在很大程度上仍然未知。在这里,我们整合了肿瘤条码化、CRISPR/Cas9 介导的基因组编辑和超深度条码测序,以在人类肺腺癌的自发小鼠模型中研究肿瘤抑制因子改变的两两组合。我们绘制了 31 种常见肺腺癌基因型的肿瘤抑制作用图谱,并确定了一个上下文依赖性和差异效应强度的景观。