| Literature DB >> 30996127 |
Alex Miranda1, Phineas T Hamilton1, Allen W Zhang2,3,4, Swetansu Pattnaik5, Etienne Becht6, Artur Mezheyeuski7, Jarle Bruun8, Patrick Micke7, Aurélien de Reynies9, Brad H Nelson10,11,12.
Abstract
Regulatory programs that control the function of stem cells are active in cancer and confer properties that promote progression and therapy resistance. However, the impact of a stem cell-like tumor phenotype ("stemness") on the immunological properties of cancer has not been systematically explored. Using gene-expression-based metrics, we evaluated the association of stemness with immune cell infiltration and genomic, transcriptomic, and clinical parameters across 21 solid cancers. We found pervasive negative associations between cancer stemness and anticancer immunity. This occurred despite high stemness cancers exhibiting increased mutation load, cancer-testis antigen expression, and intratumoral heterogeneity. Stemness was also strongly associated with cell-intrinsic suppression of endogenous retroviruses and type I IFN signaling, and increased expression of multiple therapeutically accessible immunosuppressive pathways. Thus, stemness is not only a fundamental process in cancer progression but may provide a mechanistic link between antigenicity, intratumoral heterogeneity, and immune suppression across cancers.Entities:
Keywords: antitumor immunity; cancer stemness; intratumoral heterogeneity
Year: 2019 PMID: 30996127 PMCID: PMC6500180 DOI: 10.1073/pnas.1818210116
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205