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De novo pyrimidine biosynthesis inhibition synergizes with BCL-XL targeting in pancreatic cancer

ABSTRACT: Oncogenic KRAS induces metabolic rewiring in pancreatic adenocarcinoma (PDAC) characterized, in part, by dependency on de novo pyrimidine biosynthesis. Pharmacologic inhibition of dihydroorotate dehydrogenase (DHODH), an enzyme in the de novo pyrimidine synthesis pathway, delays pancreatic tumor growth; however, limited monotherapy efficacy suggests that compensatory pathways may drive resistance. Here, we use an integrated metabolomic, proteomic and in vitro and in vivo DHODH inhibitor-anchored genetic screening approach to identify compensatory pathways to DHODH inhibition (DHODHi) and targets for combination therapy strategies. We demonstrate that DHODHi alters the apoptotic regulatory proteome thereby enhancing sensitivity to inhibitors of the anti-apoptotic BCL2L1 (BCL-XL) protein. Co-targeting DHODH and BCL-XL synergistically induces apoptosis in PDAC cells and patient-derived organoids. The combination of DHODH inhibition with Brequinar and BCL-XL degradation by DT2216, a proteolysis targeting chimera (PROTAC), significantly inhibits PDAC tumor growth. These data define mechanisms of adaptation to DHODHi and support combination therapy targeting BCL-XL in PDAC.

INSTRUMENT(S): QTRAP 5500

ORGANISM(S): Homo Sapiens (ncbitaxon:9606)

SUBMITTER: Joseph D. Mancias Naiara Santana Codina

PROVIDER: MSV000097577 | MassIVE | Wed Apr 09 11:07:00 BST 2025

REPOSITORIES: MassIVE

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De novo pyrimidine biosynthesis inhibition synergizes with BCL-XL targeting in pancreatic cancer

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