hENT Inhibition Prevents Pyrimidine-Driven Resistance to DHODH Inhibition in Malignant Rhabdoid Tumors
Marjolein M G KesiD, Giulia PerticariiD, Jolanda Kooiman, Nadia Anderson, Jeroen W. A. JanseniD, Esther A. ZaaliD, Celia R. BerkersiD, Jarno DrostiD
Abstract
Extracranial malignant rhabdoid tumors (ecMRTs) are aggressive pediatric cancers characterized by mutations in genes encoding members of the SWItch/Sucrose Non-Fermentable (SWI/SNF) chromatin remodeling complex, with limited effective treatment options. Metabolic reprogramming, including nucleotide biosynthesis, is a hallmark of cancer that represents a potential therapeutic vulnerability. Previously, we demonstrated that inhibition of the de novo pyrimidine synthesis enzyme dihydroorotate dehydrogenase (DHODH) represents a promising treatment strategy for rhabdoid tumors, including ecMRTs and atypical teratoid/rhabdoid tumors (AT/RTs). Using patient-derived tumoroid models, we now extend these findings by showing that another SWI/SNF-deficient pediatric cancer, small cell carcinoma of the ovary, hypercalcemic type (SCCOHT), is also sensitive to DHODH inhibition. Gene expression analyses further confirmed that SCCOHT and AT/RT, like ecMRT, exhibit elevated expression of de novo nucleotide synthesis genes. To determine whether metabolic features of the tumor microenvironment (TME) influence DHODH inhibitor (DHODHi) response, we profiled plasma and tumor interstitial fluid from orthotopic ecMRT-bearing mice and found that the TME was markedly enriched in nucleosides and nucleobases. Supplementation of standard culture media with these nucleosides demonstrated that pyrimidines, but not purines, can rescue ecMRT cells from DHODHi-induced growth inhibition via activation of the pyrimidine salvage pathway. This resistance mechanism was effectively reversed by co-treatment with human equilibrative nucleoside transporter (hENT) inhibitors, enhancing DHODHi sensitivity in ecMRTs. Collectively, these findings reveal a conserved metabolic vulnerability across SWI/SNF-deficient pediatric cancers and emphasize the critical importance of modeling tumor metabolism under physiologically relevant conditions to accurately identify metabolism-targeted therapeutic strategies for these currently lethal pediatric cancer types.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 0
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Direct therapeutic targeting of SWI/SNF induces epigenetic reprogramming and durable tumor regression in rhabdoid tumor
M. H. Chasse, B. K. Johnson, … P. J. Grohar·bioRxiv·Dec 3, 2019
- MET inhibition exploits conserved regulatory dependencies in malignant rhabdoid tumors
Ines Sentis, Alex Cebria-Xart, … Alexandra Avgustinova·bioRxiv·Nov 4, 2026
- Acquired deficiency of the peroxisomal enzyme enoyl-CoA hydratase/3-hydroxyacyl CoA dehydrogenase is a metabolic vulnerability in hepatoblastoma
H. Wang, X. Chen, … E. V. Prochownik·bioRxiv·Aug 24, 2020
- Succinate Dehydrogenase-Deficient Cancer Cells Have Increased Susceptibility to Ym155 Induced DNA Damage
Qianjin Guo, Sooyeon Lee, … Justin P. Annes·Endocrine Related CancerPeer-reviewed·Feb 19, 2026
- Inhibition of DHODH Activates Pyroptosis and cGAS-STING Pathways to Enhance NK cell Infiltration Mediated Anti-tumor Immunity in Melanoma
Yongrui Hai, Ruizhuo Lin, … Gaofei Wei·bioRxiv·Mar 20, 2025
- Image-Guided Targeting of Mitochondrial Metabolism Sensitizes Pediatric Malignant Rhabdoid Tumors to Low Dose Radiotherapy
Wenxi Xia, Matthew Goff, … Shreya Goel·Science AdvancesPeer-reviewed·May 23, 2025