In vivo functional screening for systems-level integrative cancer genomics

被引:0
|
作者
Julia Weber
Christian J. Braun
Dieter Saur
Roland Rad
机构
[1] Technische Universität München,Institute of Molecular Oncology and Functional Genomics, TUM School of Medicine
[2] Technische Universität München,Center for Translational Cancer Research (TranslaTUM), TUM School of Medicine
[3] University Hospital,Department of Pediatrics, Dr. von Hauner Children’s Hospital
[4] LMU Munich,Department of Medicine II, Klinikum rechts der Isar
[5] Hopp Children’s Cancer Center Heidelberg (KiTZ),undefined
[6] German Cancer Research Center (DKFZ),undefined
[7] Institute of Translational Cancer Research and Experimental Cancer Therapy,undefined
[8] Klinikum rechts der Isar,undefined
[9] Technische Universität München,undefined
[10] Technische Universität München,undefined
[11] German Cancer Consortium (DKTK),undefined
[12] German Cancer Research Center (DKFZ),undefined
来源
Nature Reviews Cancer | 2020年 / 20卷
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摘要
With the genetic portraits of all major human malignancies now available, we next face the challenge of characterizing the function of mutated genes, their downstream targets, interactions and molecular networks. Moreover, poorly understood at the functional level are also non-mutated but dysregulated genomes, epigenomes or transcriptomes. Breakthroughs in manipulative mouse genetics offer new opportunities to probe the interplay of molecules, cells and systemic signals underlying disease pathogenesis in higher organisms. Herein, we review functional screening strategies in mice using genetic perturbation and chemical mutagenesis. We outline the spectrum of genetic tools that exist, such as transposons, CRISPR and RNAi and describe discoveries emerging from their use. Genome-wide or targeted screens are being used to uncover genomic and regulatory landscapes in oncogenesis, metastasis or drug resistance. Versatile screening systems support experimentation in diverse genetic and spatio-temporal settings to integrate molecular, cellular or environmental context-dependencies. We also review the combination of in vivo screening and barcoding strategies to study genetic interactions and quantitative cancer dynamics during tumour evolution. These scalable functional genomics approaches are transforming our ability to interrogate complex biological systems.
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页码:573 / 593
页数:20
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