Control of PD-L1 Expression by Oncogenic Activation of the AKT–mTOR Pathway in Non–Small Cell Lung Cancer
Johns Hopkins University · George Washington University · +5 more institutions
Abstract
Alterations in EGFR, KRAS, and ALK are oncogenic drivers in lung cancer, but how oncogenic signaling influences immunity in the tumor microenvironment is just beginning to be understood. Immunosuppression likely contributes to lung cancer, because drugs that inhibit immune checkpoints like PD-1 and PD-L1 have clinical benefit. Here, we show that activation of the AKT-mTOR pathway tightly regulates PD-L1 expression in vitro and in vivo. Both oncogenic and IFNγ-mediated induction of PD-L1 was dependent on mTOR. In human lung adenocarcinomas and squamous cell carcinomas, membranous expression of PD-L1 was significantly associated with mTOR activation. These data suggest that oncogenic activation of the AKT-mTOR…
Citation impact
- FWCI
- 23.37
- Percentile
- 100%
- References
- 52
Authors
13- KJKristin J. LastwikaCorresponding
Johns Hopkins University, George Washington University, Johns Hopkins Medicine
- WWWillie Wilson
National Cancer Institute, Center for Cancer Research, Department of Health and Human Services
- QKQing Kay Li
Johns Hopkins University, Johns Hopkins Medicine
- JWJeffrey W. Norris
Johns Hopkins University, Johns Hopkins Medicine
- HXHaiying Xu
Johns Hopkins University, Johns Hopkins Medicine
Topics & keywords
- PI3K/AKT/mTOR pathway
- Cancer research
- Protein kinase B
- Immune system
- KRAS
- Lung cancer
- Cancer
- Tumor microenvironment
- Good health and well-being