Mutant IDH inhibitors induce lineage differentiation in IDH-mutant oligodendroglioma

Avishay Spitzer(Tel Aviv University), Simon Gritsch(Broad Institute), Masashi Nomura(Broad Institute), Alexander Jucht(Broad Institute), Jérôme Fortin(Montreal Neurological Institute and Hospital), Ramya Raviram(Cornell University), Hannah Weisman(Broad Institute), L. Nicolas Gonzalez Castro(Broad Institute), Nicholas Druck(Broad Institute), Rony Chanoch-Myers(Weizmann Institute of Science), John J. Y. Lee(Broad Institute), Ravindra Mylvaganam(Harvard University), Rachel L. Servis(Harvard University), Jeremy Man Fung(Harvard University), Christine K. Lee(Harvard University), Hiroaki Nagashima(Harvard University), Julie J. Miller(Harvard University), Isabel Arrillaga‐Romany(Harvard University), David N. Louis(Harvard University), Hiroaki Wakimoto(Harvard University), Will Pisano(Brigham and Women's Hospital), Patrick Y. Wen(Harvard University), Tak W. Mak(Princess Margaret Cancer Centre), Marc Sanson(Centre National de la Recherche Scientifique), Mehdi Touat(Centre National de la Recherche Scientifique), Dan A. Landau(Cornell University), Keith L. Ligon(Dana-Farber Brigham Cancer Center), Daniel P. Cahill(Massachusetts General Hospital), Mario L. Suvà(Broad Institute), Itay Tirosh(Weizmann Institute of Science)
Cancer Cell
April 4, 2024
Cited by 53Open Access
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Abstract

A subset of patients with IDH-mutant glioma respond to inhibitors of mutant IDH (IDHi), yet the molecular underpinnings of such responses are not understood. Here, we profiled by single-cell or single-nucleus RNA-sequencing three IDH-mutant oligodendrogliomas from patients who derived clinical benefit from IDHi. Importantly, the tissues were sampled on-drug, four weeks from treatment initiation. We further integrate our findings with analysis of single-cell and bulk transcriptomes from independent cohorts and experimental models. We find that IDHi treatment induces a robust differentiation toward the astrocytic lineage, accompanied by a depletion of stem-like cells and a reduction of cell proliferation. Furthermore, mutations in NOTCH1 are associated with decreased astrocytic differentiation and may limit the response to IDHi. Our study highlights the differentiating potential of IDHi on the cellular hierarchies that drive oligodendrogliomas and suggests a genetic modifier that may improve patient stratification.


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