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 Field | Value | Language |
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dc.contributor.author | Li, Yuchen | - |
dc.contributor.author | Lim, Chaemin | - |
dc.contributor.author | Dismuke, Taylor | - |
dc.contributor.author | Malawsky, Daniel S. | - |
dc.contributor.author | Oasa, Sho | - |
dc.contributor.author | Bruce, Zara C. | - |
dc.contributor.author | Offenhäuser, Carolin | - |
dc.contributor.author | Baumgartner, Ulrich | - |
dc.contributor.author | D'Souza, Rochelle C. J. | - |
dc.contributor.author | Edwards, Stacey L. | - |
dc.contributor.author | French, Juliet D. | - |
dc.contributor.author | Ock, Lucy S. H. | - |
dc.contributor.author | Nair, Sneha | - |
dc.contributor.author | Sivakumaran, Haran | - |
dc.contributor.author | Harris, Lachlan | - |
dc.contributor.author | Tikunov, Andrey P. | - |
dc.contributor.author | Hwang, Duhyeong | - |
dc.contributor.author | Del Mar Alicea Pauneto, Coral | - |
dc.contributor.author | Maybury, Mellissa | - |
dc.contributor.author | Hassall, Timothy | - |
dc.contributor.author | Wainwright, Brandon | - |
dc.contributor.author | Kesari, Santosh | - |
dc.contributor.author | Stein, Gregory | - |
dc.contributor.author | Piper, Michael | - |
dc.contributor.author | Johns, Terrance G. | - |
dc.contributor.author | Sokolsky-Papkov, Marina | - |
dc.contributor.author | Terenius, Lars | - |
dc.contributor.author | Vukojević, Vladana | - |
dc.contributor.author | Gershon, Timothy R. | - |
dc.contributor.author | Day, Bryan W. | - |
dc.date.accessioned | 2024-06-20T00:30:14Z | - |
dc.date.available | 2024-06-20T00:30:14Z | - |
dc.date.issued | 2023 | - |
dc.identifier.citation | Research square, 2023 | en |
dc.identifier.uri | https://dora.health.qld.gov.au/qldresearchjspui/handle/1/6084 | - |
dc.description.abstract | Recurrence 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.title | Preventing recurrence in Sonic Hedgehog Subgroup Medulloblastoma using the OLIG2 inhibitor CT-179 | - |
dc.identifier.doi | 10.21203/rs.3.rs-2949436/v1 | - |
dc.relation.url | https://search.ebscohost.com/login.aspx?direct=true&AuthType=ip,athens&db=mdc&AN=37333134&site=ehost-live | - |
dc.identifier.journaltitle | Research square | - |
dc.identifier.risid | 4272 | - |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
Appears in Sites: | Children's Health Queensland Publications |
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