TMIC-56. TUMOR CELL ARCHITECTURAL HETEROGENEITY AND SPATIAL INTERACTIONS WITH THE TUMOR IMMUNE MICROENVIRONMENT IN GBM

نویسندگان

چکیده

Abstract INTRODUCTION Glioblastoma (GBM) contains cell populations with distinct metabolic requirements, fast-cycling cells harnessing aerobic glycolysis, and treatment-resistant slow-cycling (SCCs) preferentially engaging lipid metabolism. The interaction between immune tumor cells, how their heterogeneity shapes the landscape in GBM has yet to be understood. Objectives: primary objective of this project is spatially molecularly decode microenvironment a specific focus on unraveling links that underlie SCCs compartment. METHODS Multiple murine glioma lines coupled geospatial profiling were used establish communications, while various genetic pharmacological approaches applied assess effect disrupting interplay system. RESULTS We determined exhibit dependencies, involving preferential metabolism supported by enhanced fatty acid uptake. also found distribution progression regulated interactions suppressive which turn work against rejection inhibiting T anti-tumor activity. shaped marked features enhancing exchange capacities are exploited support survival functions. Importantly, sensitized tumors chemotherapy. CONCLUSION Our results reveal tumor-associated within play critical role development drug resistant tumors. This study delineates these communications assesses potential therapeutic treat GBM. insights generated from uncover fundamental principles emerging connections microenvironment, metabolism, immunity, associated vulnerabilities.

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ژورنال

عنوان ژورنال: Neuro-oncology

سال: 2022

ISSN: ['1523-5866', '1522-8517']

DOI: https://doi.org/10.1093/neuonc/noac209.1100