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- Publisher Website: 10.1016/j.ccell.2024.03.008
- Scopus: eid_2-s2.0-85189448228
- PMID: 38579724
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Article: Mutant IDH inhibitors induce lineage differentiation in IDH-mutant oligodendroglioma
Title | Mutant IDH inhibitors induce lineage differentiation in IDH-mutant oligodendroglioma |
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Authors | Spitzer, AvishayGritsch, SimonNomura, MasashiJucht, AlexanderFortin, JeromeRaviram, RamyaWeisman, Hannah R.Gonzalez Castro, L. NicolasDruck, NicholasChanoch-Myers, RonyLee, John J.Y.Mylvaganam, RavindraLee Servis, RachelFung, Jeremy ManLee, Christine K.Nagashima, HiroakiMiller, Julie J.Arrillaga-Romany, IsabelLouis, David N.Wakimoto, HiroakiPisano, WillWen, Patrick Y.Mak, Tak W.Sanson, MarcTouat, MehdiLandau, Dan A.Ligon, Keith L.Cahill, Daniel P.Suvà, Mario L.Tirosh, Itay |
Keywords | differentiation therapy glioma IDH1 ivosidenib oligodendroglioma single cell RNA-seq vorasidenib |
Issue Date | 13-May-2024 |
Publisher | Cell Press |
Citation | Cancer Cell, 2024, v. 42, n. 5, p. 904-914.e9 How to Cite? |
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. |
Persistent Identifier | http://hdl.handle.net/10722/346383 |
ISSN | 2023 Impact Factor: 48.8 2023 SCImago Journal Rankings: 17.507 |
DC Field | Value | Language |
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dc.contributor.author | Spitzer, Avishay | - |
dc.contributor.author | Gritsch, Simon | - |
dc.contributor.author | Nomura, Masashi | - |
dc.contributor.author | Jucht, Alexander | - |
dc.contributor.author | Fortin, Jerome | - |
dc.contributor.author | Raviram, Ramya | - |
dc.contributor.author | Weisman, Hannah R. | - |
dc.contributor.author | Gonzalez Castro, L. Nicolas | - |
dc.contributor.author | Druck, Nicholas | - |
dc.contributor.author | Chanoch-Myers, Rony | - |
dc.contributor.author | Lee, John J.Y. | - |
dc.contributor.author | Mylvaganam, Ravindra | - |
dc.contributor.author | Lee Servis, Rachel | - |
dc.contributor.author | Fung, Jeremy Man | - |
dc.contributor.author | Lee, Christine K. | - |
dc.contributor.author | Nagashima, Hiroaki | - |
dc.contributor.author | Miller, Julie J. | - |
dc.contributor.author | Arrillaga-Romany, Isabel | - |
dc.contributor.author | Louis, David N. | - |
dc.contributor.author | Wakimoto, Hiroaki | - |
dc.contributor.author | Pisano, Will | - |
dc.contributor.author | Wen, Patrick Y. | - |
dc.contributor.author | Mak, Tak W. | - |
dc.contributor.author | Sanson, Marc | - |
dc.contributor.author | Touat, Mehdi | - |
dc.contributor.author | Landau, Dan A. | - |
dc.contributor.author | Ligon, Keith L. | - |
dc.contributor.author | Cahill, Daniel P. | - |
dc.contributor.author | Suvà, Mario L. | - |
dc.contributor.author | Tirosh, Itay | - |
dc.date.accessioned | 2024-09-16T00:30:33Z | - |
dc.date.available | 2024-09-16T00:30:33Z | - |
dc.date.issued | 2024-05-13 | - |
dc.identifier.citation | Cancer Cell, 2024, v. 42, n. 5, p. 904-914.e9 | - |
dc.identifier.issn | 1535-6108 | - |
dc.identifier.uri | http://hdl.handle.net/10722/346383 | - |
dc.description.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. | - |
dc.language | eng | - |
dc.publisher | Cell Press | - |
dc.relation.ispartof | Cancer Cell | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | differentiation therapy | - |
dc.subject | glioma | - |
dc.subject | IDH1 | - |
dc.subject | ivosidenib | - |
dc.subject | oligodendroglioma | - |
dc.subject | single cell RNA-seq | - |
dc.subject | vorasidenib | - |
dc.title | Mutant IDH inhibitors induce lineage differentiation in IDH-mutant oligodendroglioma | - |
dc.type | Article | - |
dc.identifier.doi | 10.1016/j.ccell.2024.03.008 | - |
dc.identifier.pmid | 38579724 | - |
dc.identifier.scopus | eid_2-s2.0-85189448228 | - |
dc.identifier.volume | 42 | - |
dc.identifier.issue | 5 | - |
dc.identifier.spage | 904 | - |
dc.identifier.epage | 914.e9 | - |
dc.identifier.eissn | 1878-3686 | - |
dc.identifier.issnl | 1535-6108 | - |