| Literature DB >> 26014096 |
Eliezer M Van Allen1, Hadrien G Golay2, Yan Liu2, Shohei Koyama2, Karrie Wong2, Amaro Taylor-Weiner3, Marios Giannakis1, Maegan Harden3, Vanesa Rojas-Rudilla4, Aaron Chevalier3, Tran Thai2, Christine Lydon2, Stacy Mach2, Ada G Avila2, Joshua A Wong2, Alexandra R Rabin2, Joshua Helmkamp2, Lynette Sholl4, Scott L Carter3, Geoffrey Oxnard2, Pasi Janne5, Gad Getz6, Neal Lindeman4, Peter S Hammerman1, Levi A Garraway1, F Stephen Hodi7, Scott J Rodig8, Glenn Dranoff7, Kwok-Kin Wong9, David A Barbie10.
Abstract
PD-1 immune checkpoint blockade occasionally results in durable clinical responses in advanced metastatic cancers. However, mechanism-based predictors of response to this immunotherapy remain incompletely characterized. We performed comprehensive genomic profiling on a tumor and germline sample from a patient with refractory lung adenocarcinoma who achieved marked long-term clinical benefit from anti-PD-L1 therapy. We discovered activating somatic and germline amino acid variants in JAK3 that promoted PD-L1 induction in lung cancer cells and in the tumor immune microenvironment. These findings suggest that genomic alterations that deregulate cytokine receptor signal transduction could contribute to PD-L1 activation and engagement of the PD-1 immune checkpoint in lung cancer. ©2015 American Association for Cancer Research.Entities:
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Year: 2015 PMID: 26014096 PMCID: PMC4527885 DOI: 10.1158/2326-6066.CIR-15-0024
Source DB: PubMed Journal: Cancer Immunol Res ISSN: 2326-6066 Impact factor: 11.151