The inactive X chromosome drives sex differences in microglial inflammatory activity in human glioblastoma
Tharp, M. E.; Han, C. Z.; Talukdar, M.; Balak, C. D.; Fitzpatrick, C.; O'Connor, C.; Preissl, S.; Buchanan, J.; Nott, A.; Escoubet, L.; Mavrommatis, K.; Gupta, M.; Schwartz, M. S.; U, H. S.; Jones, P. S.; Levy, M. L.; Gonda, D. D.; Ben-Haim, S.; Ciacci, J.; Barba, D.; Khalessi, A.; Coufal, N. G.; Chen, C. C.; Glass, C. K.; Page, D. C.
Show abstract
Whether an individual is a biological female or male affects cancer risk, but the responsible mechanisms and cell types remain obscure. Glioblastoma multiforme (GBM) is a male-biased cancer that is highly aggressive, and resistant to treatment, with poor patient survival. Dismal prognoses in GBM are due in part to the specialized immune system of the brain, consisting largely of microglia, which regulate GBM development and progression. We hypothesized that microglia function differently in females and males and thereby contribute to the observed male bias in GBM. We sorted TAM-MGs (tumor-associated macrophages - microglia) from human GBMs and low-grade gliomas and performed bulk transcriptomic and epigenomic assays to identify sex-biased gene expression. We used published single-cell transcriptomic data from human GBMs to predict sex-biased TAM-MG interactions with other cell types. We found that female and male TAM-MGs mount different inflammatory responses, with female TAM-MGs displaying stronger interferon signaling and cytotoxic T-cell interactions that should enhance anti-tumor immunity in GBM. We validated these sex-differential inflammatory responses experimentally, and determined that genes on the sex chromosomes, specifically those expressed by Xi (the "inactive" X chromosome), drive these differences. Together, our results suggest that sex-differential TAM-MG inflammatory responses contribute to the higher incidence and mortality of GBM in males.
Matching journals
The top 8 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Single-nucleus and spatial landscape of the sub-ventricular zone in human glioblastoma 96%
- Defining the molecular identity and morphology of glia limitans superficialis astrocytes in mouse and human 95%
- The expression profile and tumorigenic mechanisms of CD97 (ADGRE5) in glioblastoma render it a targetable vulnerability 95%
Similar papers in this journal
- Neurons burdened by DNA double strand breaks incite microglia activation through antiviral-like signaling in neurodegeneration. 96%
- A dynamic gene regulatory code drives synaptic development of hippocampal granule cells 94%
- Immunotherapy of glioblastoma explants induces interferon-γ responses and immune cell rearrangements in tumor center, but not periphery 94%
Similar papers in this journal
- Multi-omic landscape of human gliomas from diagnosis to treatment and recurrence 96%
- Mutant IDH Inhibitors Induce Lineage Differentiation in IDH-mutant Oligodendroglioma 95%
- Single-cell landscapes of primary glioblastomas and matched organoids and cell lines reveal variable retention of inter- and intra-tumor heterogeneity 95%
Similar papers in this journal
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.