The mitochondrial NADH shuttle system is a targetable vulnerability for Group 3 medulloblastoma in a hypoxic microenvironment

• Published in: Cell death & disease 2023-11, Vol.14 (11), p.784-784, Article 784
• Main Authors: Contenti, J., Guo, Y., Mazzu, A., Irondelle, M., Rouleau, M., Lago, C., Leva, G., Tiberi, L., Ben-Sahra, I., Bost, F., Mazure, N. M.
• Format: Article
• Language: English
• Subjects: 13/1; 13/2; 14/19; 38/39; 631/154/555; 631/67/2327; 631/67/2332; 631/67/327; 631/80/82/23; 82/80; Antibodies; Apoptosis; Aspartic Acid - metabolism; Biochemistry; Biomedical and Life Sciences; Brain cancer; Brain tumors; Cancer; Cell Biology; Cell Culture; Cell death; Cell proliferation; Cellular Biology; Cerebellar Neoplasms - genetics; Cerebellum; Chemotherapy; Child; Glycerol; Human health and pathology; Humans; Hypoxia; Immunology; L-Lactate dehydrogenase; Life Sciences; Malates - metabolism; Medulloblastoma; Medulloblastoma - genetics; Metabolism; Microenvironments; Mitochondria; NAD - metabolism; NADH; Neurobiology; Neurons and Cognition; Organoids; Oxygen; Pediatrics; Radiation therapy; Subcellular Processes; Tumor cells; Tumor Microenvironment
• ISSN: 2041-4889; 2041-4889
• DOI: 10.1038/s41419-023-06275-0

Medulloblastoma is a cancerous brain tumor that affects mostly children. Among the four groups defined by molecular characteristics, Group 3, the least well characterized, is also the least favorable, with a survival rate of 50%. Current treatments, based on surgery, radiotherapy, and chemotherapy, are not adequate and the lack of understanding of the different molecular features of Group 3 tumor cells makes the development of effective therapies challenging. In this study, the problem of medulloblastoma is approached from a metabolic standpoint in a low oxygen microenvironment. We establish that Group 3 cells use both the mitochondrial glycerol-3 phosphate (G3PS) and malate-aspartate shuttles (MAS) to produce NADH. Small molecules that target G3PS and MAS show a greater ability to decrease cell proliferation and induce apoptosis specifically of Group 3 cells. In addition, as Group 3 cells show improved respiration in hypoxia, the use of Phenformin, a mitochondrial complex 1 inhibitor, alone or in combination, induced significant cell death. Furthermore, inhibition of the cytosolic NAD+ recycling enzyme lactate dehydrogenase A (LDHA), enhanced the effects of the NADH shuttle inhibitors. In a 3D model using Group 3 human cerebellar organoids, tumor cells also underwent apoptosis upon treatment with NADH shuttle inhibitors. Our study demonstrates metabolic heterogeneity depending on oxygen concentrations and provides potential therapeutic solutions for patients in Group 3 whose tumors are the most aggressive.