Guernet Alexis, Mungamuri Sathish Kumar, Cartier Dorthe, Sachidanandam Ravi, Jayaprakash Anitha, Adriouch Sahil, Vezain Myriam, Charbonnier Françoise, Rohkin Guy, Coutant Sophie, Yao Shen, Ainani Hassan, Alexandre David, Tournier Isabelle, Boyer Olivier, Aaronson Stuart A, Anouar Youssef, Grumolato Luca
Normandie Univ, UNIROUEN, INSERM, DC2N, 76000 Rouen, France; Institute for Research and Innovation in Biomedicine (IRIB), 76000 Rouen, France.
Department of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Mol Cell. 2016 Aug 4;63(3):526-38. doi: 10.1016/j.molcel.2016.06.017. Epub 2016 Jul 21.
Intratumor genetic heterogeneity underlies the ability of tumors to evolve and adapt to different environmental conditions. Using CRISPR/Cas9 technology and specific DNA barcodes, we devised a strategy to recapitulate and trace the emergence of subpopulations of cancer cells containing a mutation of interest. We used this approach to model different mechanisms of lung cancer cell resistance to EGFR inhibitors and to assess effects of combined drug therapies. By overcoming intrinsic limitations of current approaches, CRISPR-barcoding also enables investigation of most types of genetic modifications, including repair of oncogenic driver mutations. Finally, we used highly complex barcodes inserted at a specific genome location as a means of simultaneously tracing the fates of many thousands of genetically labeled cancer cells. CRISPR-barcoding is a straightforward and highly flexible method that should greatly facilitate the functional investigation of specific mutations, in a context that closely mimics the complexity of cancer.
肿瘤内基因异质性是肿瘤进化并适应不同环境条件的能力基础。利用CRISPR/Cas9技术和特定的DNA条形码,我们设计了一种策略来重现和追踪含有感兴趣突变的癌细胞亚群的出现。我们用这种方法来模拟肺癌细胞对EGFR抑制剂耐药的不同机制,并评估联合药物治疗的效果。通过克服当前方法的内在局限性,CRISPR条形码技术还能够研究大多数类型的基因修饰,包括致癌驱动基因突变的修复。最后,我们将高度复杂的条形码插入特定基因组位置,以此同时追踪数千个基因标记癌细胞的命运。CRISPR条形码技术是一种直接且高度灵活的方法,在紧密模拟癌症复杂性的背景下,应能极大地促进对特定突变的功能研究。