Multi-pronged analysis of pediatric low-grade glioma reveals a unique tumor microenvironment associated with BRAF alterations.
Shadi ZahediKent A RiemondyAndrea M GriesingerAndrew M DonsonRui FuMichele CrespoJohn DeSistoMadeline M GroatEmil BratbakAdam GreenTodd C HankinsonMichael HandlerRajeev VibhakarNicholas WillardNicholas K ForemanJean Mulcahy LevyPublished in: bioRxiv : the preprint server for biology (2024)
While scRNA seq provides information on cellular heterogeneity within the tumor microenvironment (TME), it does not provide a complete picture of how these cells are interacting or where they are located. To expand on this, we used a three-pronged approach to better understand the biology of pediatric low-grade glioma (pLGG). By analyzing scRNA-seq, secreted cytokines and spatial orientation of cells within the TME, we strove to gain a more complete picture of the complex interplay between tumor and immune cells within pLGG. Our data revealed a complex heterogeneity in tumor and immune populations and identified an interesting difference in the immune phenotype among different subtypes.
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