EXTH-20. Genetic modeling of ELP1-associated Sonic hedgehog medulloblastoma identifies MDM2 as a selective therapeutic target

Abstract Germline loss-of-function (LOF) variants in Elongator acetyltransferase complex subunit 1 (ELP1) are the most prevalent predisposing genetic events observed in medulloblastoma (MB), accounting for 30% of the Sonic hedgehog (SHH) 3 subtype. Molecularly, ELP1-associated SHH-MBs acquire somatic PTCH1 mutations in >80% of cases, and universal loss-of-heterozygosity of the wild-type ELP1 and PTCH1 alleles through loss of chromosome-arm 9q, resulting in their biallelic inactivation. Notably, germline ELP1 LOF occurs mostly mutually exclusive with TP53 LOF mutations in the SHH-3 subtype, suggesting that genetic perturbation of either ELP1 or TP53 may elicit similar tumorigenic consequences in cerebellar granule neuron progenitors (GNPs), the accepted cellular origin of SHH-MB. Despite these findings, the molecular, biochemical, and cellular mechanism(s) by which ELP1-deficiency provokes SHH-MB pathogenesis remain unknown. In this study, we sought to close this knowledge gap and functionally determine why children harboring pathogenic ELP1 germline variants are at an increased risk of developing SHH-MB. Mice were genetically engineered to mimic heterozygous Elp1 LOF (Elp1HET). We studied the effect of Elp1 LOF in GNPs using a combination of multi-omics approaches, immunohistological, and functional assays. GNPs from Elp1HET mice exhibited a spectrum of molecular and biochemical hallmarks of malignant transformation including increased DNA replication stress, DNA damage, accelerated cell cycle, and stalled differentiation. Orthotopic transplantation of Elp1HET GNPs engineered to harbor somatic Ptch1 inactivation yielded SHH-MB-like tumors with compromised p53 signaling, providing an explanation for the specificity of ELP1-associated tumors in SHH-3, and their exclusivity with TP53-mutant tumors. Treatment of ELP1-mutant patient-derived xenografts with an FDA-approved MDM2 inhibitor reactivated p53-dependent apoptosis and extended survival. Collectively, our findings functionally substantiate the role of ELP1 deficiency in predisposition to SHH-3 MB and nominate therapeutics targeting MDM2 to overcome p53 inhibition as a rational treatment option.

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Journal
Neuro-Oncology
Published
2025-11-01
DOI
https://doi.org/10.1093/neuonc/noaf201.1354
Primary Topic
Hedgehog Signaling Pathway Studies
Type
article
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article

EXTH-20. Genetic modeling of ELP1-associated Sonic hedgehog medulloblastoma identifies MDM2 as a selective therapeutic target

Lena M. Kutscher, Brandon J. Wainwright, Suzanne J. Baker, Jennifer L. Hadley et al.
Neuro-Oncology
Hedgehog Signaling Pathway Studies
article

EXTH-20. Genetic modeling of ELP1-associated Sonic hedgehog medulloblastoma identifies MDM2 as a selective therapeutic target

Lena M. Kutscher, Brandon J. Wainwright, Suzanne J. Baker, Jennifer L. Hadley, Martine F. Roussel, Zoran Ranković, Taha Soliman, Jesús García-López, Alaa Refaat, Brent A. Orr, Shiekh Tanveer Ahmad, Abbas Shirinifard, Aaron Pitre, Amar Gajjar, Stefan M. Pfister, Leena Paul, Brandon Bianski, Paul A. Northcott, Sebastian M. Waszak, Melissa Batts, Christopher L. Tinkle, Giles W Robinson, Brian Gudenas, Frédérique Zindy, Marija Kojic, Nathaniel Twarog, Alun Jones, Meifen Lu, Anand Mayasundari, Arzu Onar‐Thomas, Hong Lin, Stephanie Wu, Sara A. Lewis, Anang A. Shelat, Laura J. Janke, Yiran Li, Frederik Arnskötter
article en

Abstract

Abstract Germline loss-of-function (LOF) variants in Elongator acetyltransferase complex subunit 1 (ELP1) are the most prevalent predisposing genetic events observed in medulloblastoma (MB), accounting for 30% of the Sonic hedgehog (SHH) 3 subtype. Molecularly, ELP1-associated SHH-MBs acquire somatic PTCH1 mutations in >80% of cases, and universal loss-of-heterozygosity of the wild-type ELP1 and PTCH1 alleles through loss of chromosome-arm 9q, resulting in their biallelic inactivation. Notably, germline ELP1 LOF occurs mostly mutually exclusive with TP53 LOF mutations in the SHH-3 subtype, suggesting that genetic perturbation of either ELP1 or TP53 may elicit similar tumorigenic consequences in cerebellar granule neuron progenitors (GNPs), the accepted cellular origin of SHH-MB. Despite these findings, the molecular, biochemical, and cellular mechanism(s) by which ELP1-deficiency provokes SHH-MB pathogenesis remain unknown. In this study, we sought to close this knowledge gap and functionally determine why children harboring pathogenic ELP1 germline variants are at an increased risk of developing SHH-MB. Mice were genetically engineered to mimic heterozygous Elp1 LOF (Elp1HET). We studied the effect of Elp1 LOF in GNPs using a combination of multi-omics approaches, immunohistological, and functional assays. GNPs from Elp1HET mice exhibited a spectrum of molecular and biochemical hallmarks of malignant transformation including increased DNA replication stress, DNA damage, accelerated cell cycle, and stalled differentiation. Orthotopic transplantation of Elp1HET GNPs engineered to harbor somatic Ptch1 inactivation yielded SHH-MB-like tumors with compromised p53 signaling, providing an explanation for the specificity of ELP1-associated tumors in SHH-3, and their exclusivity with TP53-mutant tumors. Treatment of ELP1-mutant patient-derived xenografts with an FDA-approved MDM2 inhibitor reactivated p53-dependent apoptosis and extended survival. Collectively, our findings functionally substantiate the role of ELP1 deficiency in predisposition to SHH-3 MB and nominate therapeutics targeting MDM2 to overcome p53 inhibition as a rational treatment option.

Neuro-OncologyVol. 27(Supplement_5)
Translational Research Institute (AU), St. Jude Children's Research Hospital (US), The University of Queensland (AU), German Cancer Research Center (DE), Heidelberg University (DE), University Hospital Heidelberg (DE), National Center for Tumor Diseases (DE), Hopp Children's Cancer Center Heidelberg (DE), École Polytechnique Fédérale de Lausanne (CH)
Openalex Percentile: Top 70%
Hedgehog Signaling Pathway Studies
DOISourceOpenAlex
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