The Immune Landscape of Cancer
Epigenome
DOI:
10.1016/j.immuni.2018.03.023
Publication Date:
2018-04-05T21:54:55Z
AUTHORS (782)
ABSTRACT
We performed an extensive immunogenomic analysis of more than 10,000 tumors comprising 33 diverse cancer types by utilizing data compiled TCGA. Across types, we identified six immune subtypes—wound healing, IFN-γ dominant, inflammatory, lymphocyte depleted, immunologically quiet, and TGF-β dominant—characterized differences in macrophage or signatures, Th1:Th2 cell ratio, extent intratumoral heterogeneity, aneuploidy, neoantigen load, overall proliferation, expression immunomodulatory genes, prognosis. Specific driver mutations correlated with lower (CTNNB1, NRAS, IDH1) higher (BRAF, TP53, CASP8) leukocyte levels across all cancers. Multiple control modalities the intracellular extracellular networks (transcription, microRNAs, copy number, epigenetic processes) were involved tumor-immune interactions, both within subtypes. Our immunogenomics pipeline to characterize these heterogeneous resulting are intended serve as a resource for future targeted studies further advance field.
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