Convergent Identification and Interrogation of Tumor-Intrinsic Factors that Modulate Cancer Immunity In Vivo

被引:13
|
作者
Codina, Adan [1 ,2 ,3 ,4 ]
Renauer, Paul A. [1 ,2 ,3 ,4 ]
Wang, Guangchuan [1 ,2 ,3 ]
Chow, Ryan D. [1 ,2 ,3 ,5 ]
Park, Jonathan J. [1 ,2 ,3 ,5 ]
Ye, Hanghui [1 ,2 ,3 ]
Zhang, Kerou [3 ,6 ]
Dong, Matthew B. [1 ,2 ,3 ,5 ]
Gassaway, Brandon [1 ,3 ,13 ]
Ye, Lupeng [1 ,2 ,3 ]
Errami, Youssef [1 ,2 ,3 ]
Shen, Li [1 ,2 ,3 ]
Chang, Alan [1 ,2 ,3 ]
Jain, Dhanpat [7 ,8 ]
Herbst, Roy S. [8 ,9 ,10 ,11 ]
Bosenberg, Marcus [7 ,11 ,12 ]
Rinehart, Jesse [1 ,3 ,13 ]
Fan, Rong [3 ,6 ]
Chen, Sidi [1 ,2 ,3 ,4 ,5 ,11 ,14 ,15 ]
机构
[1] Integrated Sci & Technol Ctr, Syst Biol Inst, 850 West Campus Dr, West Haven, CT 06516 USA
[2] Yale Univ, Sch Med, Dept Genet, 333 Cedar St, New Haven, CT 06510 USA
[3] Integrated Sci & Technol Ctr, Ctr Canc Syst Biol, 850 West Campus Dr, West Haven, CT 06516 USA
[4] Yale Univ, MCGD Program, 333 Cedar St, New Haven, CT 06510 USA
[5] Yale MD PhD Program, 367 Cedar St, New Haven, CT 06510 USA
[6] Yale Univ, Dept Biomed Engn, 55 Prospect St, New Haven, CT 06511 USA
[7] Yale Univ, Sch Med, Dept Pathol, New Haven, CT 06510 USA
[8] Yale Univ, Sch Med, Dept Med, New Haven, CT 06510 USA
[9] Yale Univ, Sch Med, Dept Pharmacol, New Haven, CT 06510 USA
[10] Smilow Canc Hosp, 35 Pk St, New Haven, CT 06510 USA
[11] Yale Comprehens Canc Ctr, 20 York St,Ste North Pavil 4, New Haven, CT 06510 USA
[12] Yale Univ, Sch Med, Dept Dermatol, New Haven, CT 06510 USA
[13] Yale Univ, Dept Cellular & Mol Physiol, 333 Cedar St, New Haven, CT 06520 USA
[14] Anlyan Ctr, Immunobiol Program, 300 Cedar St, New Haven, CT 06520 USA
[15] Yale Univ, Sch Med, Yale Stem Cell Ctr, New Haven, CT 06510 USA
关键词
PD-L1; EXPRESSION; GENE-EXPRESSION; ACQUIRED-RESISTANCE; CARNEY COMPLEX; BETA-CATENIN; CELLS; PRKAR1A; ACTIVATION; KNOCKOUT; PATHWAY;
D O I
10.1016/j.cels.2019.01.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:136 / +
页数:23
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