| Literature DB >> 30797773 |
Adan Codina1, Paul A Renauer1, Guangchuan Wang2, Ryan D Chow3, Jonathan J Park3, Hanghui Ye2, Kerou Zhang4, Matthew B Dong3, Brandon Gassaway5, Lupeng Ye2, Youssef Errami2, Li Shen2, Alan Chang2, Dhanpat Jain6, Roy S Herbst7, Marcus Bosenberg8, Jesse Rinehart5, Rong Fan4, Sidi Chen9.
Abstract
The genetic makeup of cancer cells directs oncogenesis and influences the tumor microenvironment. In this study, we massively profiled genes that functionally drive tumorigenesis using genome-scale in vivo CRISPR screens in hosts with different levels of immunocompetence. As a convergent hit from these screens, Prkar1a mutant cells are able to robustly outgrow as tumors in fully immunocompetent hosts. Functional interrogation showed that Prkar1a loss greatly altered the transcriptome and proteome involved in inflammatory and immune responses as well as extracellular protein production. Single-cell transcriptomic profiling and flow cytometry analysis mapped the tumor microenvironment of Prkar1a mutant tumors and revealed the transcriptomic alterations in host myeloid cells. Taken together, our data suggest that tumor-intrinsic mutations in Prkar1a lead to drastic alterations in the genetic program of cancer cells, thereby remodeling the tumor microenvironment.Entities:
Keywords: Prkar1a; cancer genomics; cancer immunology; in vivo CRISPR screen; transformation
Mesh:
Year: 2019 PMID: 30797773 PMCID: PMC6592847 DOI: 10.1016/j.cels.2019.01.004
Source DB: PubMed Journal: Cell Syst ISSN: 2405-4712 Impact factor: 10.304