Scientific publications
Mutant-IDH inhibits Interferon- TET2 signaling to promote immunoevasion and tumor maintenance in cholangiocarcinoma. Scientific Publication
Meng-Ju Wu # 1 2, Lei Shi # 1 2, Juan Dubrot # 2 3, Joshua Merritt 1, Vindhya Vijay 1, Ting-Yu Wei 1, Emily Kessler 2 3, Kira E Olander 2 3, Ramzi Adil 1, Amaya Pankaj 1 4, Krishna Seshu Tummala 1, Vajira Weeresekara 1, Yuanli Zhen 1, Qibiao Wu 1, Meiqi Luo 5, William Shen 6, María García-Beccaria 7, Mirian Fernández-Vaquero 7, Christine Hudson 8, Sebastien Ronseaux 8, Yi Sun 1, Rodrigo Saad-Berreta 1, Russell W Jenkins 1, Tong Wang 9, Mathias Heikenwälder 7, Cristina R Ferrone 10, Lipika Goyal 1, Brandon Nicolay 8, Vikram Deshpande 1 4, Rahul M Kohli 5 11, Hongwu Zheng 12, Robert T Manguso 2 3, Nabeel Bardeesy 1 2
Abstract
Isocitrate dehydrogenase 1 mutations (mIDH1) are common in cholangiocarcinoma. (R)-2-hydroxyglutarate generated by the mIDH1 enzyme inhibits multiple α-ketoglutarate-dependent enzymes, altering epigenetics and metabolism. Here, by developing mIDH1-driven genetically engineered mouse models, we show that mIDH1 supports cholangiocarcinoma tumor maintenance through an immunoevasion program centered on dual (R)-2-hydroxyglutarate-mediated mechanisms: suppression of CD8+ T-cell activity and tumor cell-autonomous inactivation of TET2 DNA demethylase. Pharmacologic mIDH1 inhibition stimulates CD8+ T-cell recruitment and interferon γ (IFNγ) expression and promotes TET2-dependent induction of IFNγ response genes in tumor cells. CD8+ T-cell depletion or tumor cell-specific ablation of TET2 or IFNγ receptor 1 causes treatment resistance. Whereas immune-checkpoint activation limits mIDH1 inhibitor efficacy, CTLA4 blockade overcomes immunosuppression, providing therapeutic synergy. The findings in this mouse model of cholangiocarcinoma demonstrate that immune function and the IFNγ-TET2 axis are essential for response to mIDH1 inhibition and suggest a novel strategy for potentiating efficacy.
Significance: Mutant IDH1 inhibition stimulates cytotoxic T-cell function and derepression of the DNA demethylating enzyme TET2, which is required for tumor cells to respond to IFNγ. The discovery of mechanisms of treatment efficacy and the identification of synergy by combined CTLA4 blockade provide the foundation for new therapeutic strategies. See related commentary by Zhu and Kwong, p. 604. This article is highlighted in the In This Issue feature, p. 587.
CITATION Cancer Discov. 2022 Mar 1;12(3):812-835. doi: 10.1158/2159-8290.CD-21-1077.
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