Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/6084
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dc.contributor.authorLi, Yuchen-
dc.contributor.authorLim, Chaemin-
dc.contributor.authorDismuke, Taylor-
dc.contributor.authorMalawsky, Daniel S.-
dc.contributor.authorOasa, Sho-
dc.contributor.authorBruce, Zara C.-
dc.contributor.authorOffenhäuser, Carolin-
dc.contributor.authorBaumgartner, Ulrich-
dc.contributor.authorD'Souza, Rochelle C. J.-
dc.contributor.authorEdwards, Stacey L.-
dc.contributor.authorFrench, Juliet D.-
dc.contributor.authorOck, Lucy S. H.-
dc.contributor.authorNair, Sneha-
dc.contributor.authorSivakumaran, Haran-
dc.contributor.authorHarris, Lachlan-
dc.contributor.authorTikunov, Andrey P.-
dc.contributor.authorHwang, Duhyeong-
dc.contributor.authorDel Mar Alicea Pauneto, Coral-
dc.contributor.authorMaybury, Mellissa-
dc.contributor.authorHassall, Timothy-
dc.contributor.authorWainwright, Brandon-
dc.contributor.authorKesari, Santosh-
dc.contributor.authorStein, Gregory-
dc.contributor.authorPiper, Michael-
dc.contributor.authorJohns, Terrance G.-
dc.contributor.authorSokolsky-Papkov, Marina-
dc.contributor.authorTerenius, Lars-
dc.contributor.authorVukojević, Vladana-
dc.contributor.authorGershon, Timothy R.-
dc.contributor.authorDay, Bryan W.-
dc.date.accessioned2024-06-20T00:30:14Z-
dc.date.available2024-06-20T00:30:14Z-
dc.date.issued2023-
dc.identifier.citationResearch square, 2023en
dc.identifier.urihttps://dora.health.qld.gov.au/qldresearchjspui/handle/1/6084-
dc.description.abstractRecurrence is the primary life-threatening complication for medulloblastoma (MB). In Sonic Hedgehog (SHH)-subgroup MB, OLIG2-expressing tumor stem cells drive recurrence. We investigated the anti-tumor potential of the small-molecule OLIG2 inhibitor CT-179, using SHH-MB patient-derived organoids, patient-derived xenograft (PDX) tumors and mice genetically-engineered to develop SHH-MB. CT-179 disrupted OLIG2 dimerization, DNA binding and phosphorylation and altered tumor cell cycle kinetics in vitro and in vivo , increasing differentiation and apoptosis. CT-179 increased survival time in GEMM and PDX models of SHH-MB, and potentiated radiotherapy in both organoid and mouse models, delaying post-radiation recurrence. Single cell transcriptomic studies (scRNA-seq) confirmed that CT-179 increased differentiation and showed that tumors up-regulated Cdk4 post-treatment. Consistent with increased CDK4 mediating CT-179 resistance, CT-179 combined with CDK4/6 inhibitor palbociclib delayed recurrence compared to either single-agent. These data show that targeting treatment-resistant MB stem cell populations by adding the OLIG2 inhibitor CT-179 to initial MB treatment can reduce recurrence.; Competing Interests: Additional Declarations: Yes there is potential Competing Interest. G.S. is Chief Executive Officer, Chairman of the Board, and has equity ownership at Curtana Pharmaceuticals. S.K. is a member of the Board and has equity ownership at Curtana Pharmaceuticals. The other co-authors have no competing interests to report.-
dc.titlePreventing recurrence in Sonic Hedgehog Subgroup Medulloblastoma using the OLIG2 inhibitor CT-179-
dc.identifier.doi10.21203/rs.3.rs-2949436/v1-
dc.relation.urlhttps://search.ebscohost.com/login.aspx?direct=true&AuthType=ip,athens&db=mdc&AN=37333134&site=ehost-live-
dc.identifier.journaltitleResearch square-
dc.identifier.risid4272-
item.fulltextNo Fulltext-
item.grantfulltextnone-
Appears in Sites:Children's Health Queensland Publications
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