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De novo pyrimidine synthesis is a targetable vulnerability in IDH mutant glioma.

Authors :
Shi DD
Savani MR
Levitt MM
Wang AC
Endress JE
Bird CE
Buehler J
Stopka SA
Regan MS
Lin YF
Puliyappadamba VT
Gao W
Khanal J
Evans L
Lee JH
Guo L
Xiao Y
Xu M
Huang B
Jennings RB
Bonal DM
Martin-Sandoval MS
Dang T
Gattie LC
Cameron AB
Lee S
Asara JM
Kornblum HI
Mak TW
Looper RE
Nguyen QD
Signoretti S
Gradl S
Sutter A
Jeffers M
Janzer A
Lehrman MA
Zacharias LG
Mathews TP
Losman JA
Richardson TE
Cahill DP
DeBerardinis RJ
Ligon KL
Xu L
Ly P
Agar NYR
Abdullah KG
Harris IS
Kaelin WG Jr
McBrayer SK
Source :
Cancer cell [Cancer Cell] 2022 Sep 12; Vol. 40 (9), pp. 939-956.e16. Date of Electronic Publication: 2022 Aug 18.
Publication Year :
2022

Abstract

Mutations affecting isocitrate dehydrogenase (IDH) enzymes are prevalent in glioma, leukemia, and other cancers. Although mutant IDH inhibitors are effective against leukemia, they seem to be less active in aggressive glioma, underscoring the need for alternative treatment strategies. Through a chemical synthetic lethality screen, we discovered that IDH1-mutant glioma cells are hypersensitive to drugs targeting enzymes in the de novo pyrimidine nucleotide synthesis pathway, including dihydroorotate dehydrogenase (DHODH). We developed a genetically engineered mouse model of mutant IDH1-driven astrocytoma and used it and multiple patient-derived models to show that the brain-penetrant DHODH inhibitor BAY 2402234 displays monotherapy efficacy against IDH-mutant gliomas. Mechanistically, this reflects an obligate dependence of glioma cells on the de novo pyrimidine synthesis pathway and mutant IDH's ability to sensitize to DNA damage upon nucleotide pool imbalance. Our work outlines a tumor-selective, biomarker-guided therapeutic strategy that is poised for clinical translation.<br />Competing Interests: Declaration of interests R.J.D., W.G.K., and S.K.M. have served as paid advisors to Agios Pharmaceuticals. W.G.K. receives compensation for roles as an Eli Lilly and LifeMine Therapeutics Board Director, a founder of Tango Therapeutics and Cedilla Therapeutics, and a scientific advisor for Fibrogen, IconOVir Bio, Circle Pharma, Nextext Invest, and Casdin Capital. K.L.L. receives research support from Eli Lilly and Company via the DFCI. S.K.M. and W.G.K. received research funding from Bayer Pharmaceuticals. Bayer had no influence over the design, execution, or interpretation of studies. N.Y.R.A. is key opinion leader for Bruker Daltonics, scientific advisor to Invicro, and receives support from Thermo Finnegan and EMD Serono. S.G., A.S., M.S., A.J., and L.E. are employees at Bayer. S.G., A.S., and A.J. hold stock in Bayer. D.P.C. has consulted for Lilly, GlaxoSmithKline, and Boston Pharmaceuticals and serves on the advisory board of Pyramid Biosciences, which includes an equity interest. All other authors declare no competing interests.<br /> (Copyright © 2022 The Author(s). Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1878-3686
Volume :
40
Issue :
9
Database :
MEDLINE
Journal :
Cancer cell
Publication Type :
Academic Journal
Accession number :
35985343
Full Text :
https://doi.org/10.1016/j.ccell.2022.07.011