CBMS-5 One-carbon metabolism protect glioma cells under glutamine starvation through upregulation of MTHFD2

• Published in: Neuro-oncology advances Vol. 3; no. Supplement_6; pp. vi2 - vi3
• Main Authors: Tanaka, Kazuhiro, Nagashima, Hiroaki, Uno, Takiko, Fujita, Yuichi, Iwahashi, Hirofumi, Sasayama, Takashi
• Format: Journal Article
• Language: English
• Published: US Oxford University Press 06-12-2021
• Subjects: Supplement Abstracts
• ISSN: 2632-2498; 2632-2498
• DOI: 10.1093/noajnl/vdab159.007

Cancer cells optimize nutrient utilization to supply energetic and biosynthetic pathways. However, less is known about how cancer cells exhibit metabolic flexibility to sustain cell growth and survival from nutrient starvation. Here, we find that serine and glycine levels were higher in low-nutrient regions of tumors in glioblastoma multiforme (GBM) patients than they were in other regions. Metabolic and functional studies demonstrated that serine availability and one-carbon metabolism support glioma cell survival following glutamine deprivation. Serine synthesis was mediated through autophagy rather than glycolysis. Gene expression analysis identified upregulation of methylenetetrahydrofolate dehydrogenase 2 (MTHFD2) to regulate one-carbon metabolism. In clinical samples, MTHFD2 expression was highest in the nutrient-poor areas around pseudopalisading necrosis. Genetic suppression of MTHFD2 and autophagy inhibition caused tumor cell death and growth inhibition of glioma cells upon glutamine deprivation. These results suggest new therapeutic targets for glioma cells adapting to a low-nutrient microenvironment.