| Literature DB >> 32130895 |
Sahar Shahamatdar1, Meng Xiao He2, Matthew A Reyna3, Alexander Gusev4, Saud H AlDubayan4, Eliezer M Van Allen5, Sohini Ramachandran6.
Abstract
The immune composition of the tumor microenvironment influences response and resistance to immunotherapies. While numerous studies have identified somatic correlates of immune infiltration, germline features that associate with immune infiltrates in cancers remain incompletely characterized. We analyze seven million autosomal germline variants in the TCGA cohort and test for association with established immune-related phenotypes that describe the tumor immune microenvironment. We identify one SNP associated with the amount of infiltrating follicular helper T cells; 23 candidate genes, some of which are involved in cytokine-mediated signaling and others containing cancer-risk SNPs; and networks with genes that are part of the DNA repair and transcription elongation pathways. In addition, we find a positive association between polygenic risk for rheumatoid arthritis and amount of infiltrating CD8+ T cells. Overall, we identify multiple germline genetic features associated with tumor-immune phenotypes and develop a framework for probing inherited features that contribute to differences in immune infiltration.Entities:
Keywords: SNPs; cancer; germline; gwas; immune; immunotherapy; somatic
Mesh:
Year: 2020 PMID: 32130895 PMCID: PMC7082123 DOI: 10.1016/j.celrep.2020.02.039
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423