Abstract A052 Project HOPE: A spatiotemporal single-cell landscape of high-grade gliomas in children, adolescents and young adults

Abstract Despite the growing insights into the cellular heterogeneity of pediatric brain tumors, the transcriptional changes and spatial reorganization during disease progression remain largely unexplored. Here, we present an in-depth single-cell and 10X Xenium spatial transcriptomic characterization of 24 matched pediatric high-grade gliomas (pHGGs) in children, adolescents and young adults (AYA) profiled at both diagnosis and recurrence - constituting a total of 55 tissue samples. By stratifying the transcriptional programs activated at recurrence, we identify two distinct global response sets. Hemispheric AYA tumors predominantly exhibit upregulation of extracellular matrix pathways at recurrence, whereas midline tumors preferentially activate generic stress response programs. On a cellular level, we find that heterogeneity within the malignant tumor compartment remains largely unchanged at recurrence. However, a subset of AYA patients with hemispheric pHGG shows enrichment of the neural-progenitor-like (NPC-like) tumor cell state, and compositional changes in the immune and normal cell landscape, characterized by a global decrease in myeloid cells and an increase in oligodendrocyte fractions. Those changes lead, in turn, to enhanced NPC-like tumor cell-to-oligodendrocyte interactions. Spatial analysis of our extensive cohort at unprecedented subcellular resolution further reveals distinct cellular and spatial features associated with tumor progression, particularly in the remodeling of cell-cell interactions and tumor cell neighborhoods. Overall, this study provides a comprehensive longitudinal single-cell and spatial atlas of pHGG, uncovering the extensive cellular heterogeneity associated with tumor progression. Our findings highlight the role of intrinsic and extrinsic tumor adaptations in shaping disease progression in pHGG, offering potential novel therapeutic targets. Citation Format: Sara G. Danielli, Sina Neyazi, Olivia A. Hack, Li Jiang, Costanza Lo Cascio, Andrezza Nascimento, Cuong Nguyen, Jacob Rozowsky, Ilon Liu, Owen Hoare, Karin Shamardani, Kennedy Cunliffe-Koehler, Johannes Gojo, Keith L. Ligon, Lissa Baird, Sanda Alexandrescu, Jennifer Cotter, Michael Prados, Adam Resnick, Lin Wang, Michelle Monje, Aaron Diaz, Mariella G. Filbin. Project HOPE: A spatiotemporal single-cell landscape of high-grade gliomas in children, adolescents and young adults [abstract]. In: Proceedings of the AACR Special Conference in Cancer Research: Advances in Pediatric Cancer Research; 2024 Sep 5-8; Toronto, Ontario, Canada. Philadelphia (PA): AACR; Cancer Res 2024;84(17 Suppl):Abstract nr A052.

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Journal
Cancer Research
Published
2024-09-05
DOI
https://doi.org/10.1158/1538-7445.pediatric24-a052
Primary Topic
Glioma Diagnosis and Treatment
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article
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article

Abstract A052 Project HOPE: A spatiotemporal single-cell landscape of high-grade gliomas in children, adolescents and young adults

Mariella G. Filbin, Sanda Alexandrescu, Keith Lloyd Ligon, Ilon Liu et al.
Cancer Research
Glioma Diagnosis and Treatment
article

Abstract A052 Project HOPE: A spatiotemporal single-cell landscape of high-grade gliomas in children, adolescents and young adults

Mariella G. Filbin, Sanda Alexandrescu, Keith Lloyd Ligon, Ilon Liu, Jennifer Cotter, Costanza Lo Cascio, Owen Hoare, Michelle Monje, Johannes Gojo, Sara G. Danielli, Michael D. Prados, Olivia A. Hack, Andrezza Nascimento, Karin Shamardani, Jacob S Rozowsky, Lissa Catherine Baird, Cuong Nguyen, Sina Neyazi, Adam Resnick, Kennedy Cunliffe-Koehler, Aaron A. Diaz, Li Jiang, Lin Wang
article en

Abstract

Abstract Despite the growing insights into the cellular heterogeneity of pediatric brain tumors, the transcriptional changes and spatial reorganization during disease progression remain largely unexplored. Here, we present an in-depth single-cell and 10X Xenium spatial transcriptomic characterization of 24 matched pediatric high-grade gliomas (pHGGs) in children, adolescents and young adults (AYA) profiled at both diagnosis and recurrence - constituting a total of 55 tissue samples. By stratifying the transcriptional programs activated at recurrence, we identify two distinct global response sets. Hemispheric AYA tumors predominantly exhibit upregulation of extracellular matrix pathways at recurrence, whereas midline tumors preferentially activate generic stress response programs. On a cellular level, we find that heterogeneity within the malignant tumor compartment remains largely unchanged at recurrence. However, a subset of AYA patients with hemispheric pHGG shows enrichment of the neural-progenitor-like (NPC-like) tumor cell state, and compositional changes in the immune and normal cell landscape, characterized by a global decrease in myeloid cells and an increase in oligodendrocyte fractions. Those changes lead, in turn, to enhanced NPC-like tumor cell-to-oligodendrocyte interactions. Spatial analysis of our extensive cohort at unprecedented subcellular resolution further reveals distinct cellular and spatial features associated with tumor progression, particularly in the remodeling of cell-cell interactions and tumor cell neighborhoods. Overall, this study provides a comprehensive longitudinal single-cell and spatial atlas of pHGG, uncovering the extensive cellular heterogeneity associated with tumor progression. Our findings highlight the role of intrinsic and extrinsic tumor adaptations in shaping disease progression in pHGG, offering potential novel therapeutic targets. Citation Format: Sara G. Danielli, Sina Neyazi, Olivia A. Hack, Li Jiang, Costanza Lo Cascio, Andrezza Nascimento, Cuong Nguyen, Jacob Rozowsky, Ilon Liu, Owen Hoare, Karin Shamardani, Kennedy Cunliffe-Koehler, Johannes Gojo, Keith L. Ligon, Lissa Baird, Sanda Alexandrescu, Jennifer Cotter, Michael Prados, Adam Resnick, Lin Wang, Michelle Monje, Aaron Diaz, Mariella G. Filbin. Project HOPE: A spatiotemporal single-cell landscape of high-grade gliomas in children, adolescents and young adults [abstract]. In: Proceedings of the AACR Special Conference in Cancer Research: Advances in Pediatric Cancer Research; 2024 Sep 5-8; Toronto, Ontario, Canada. Philadelphia (PA): AACR; Cancer Res 2024;84(17 Suppl):Abstract nr A052.

Cancer ResearchVol. 84(17_Supplement)
Broad Institute (US), Brigham and Women's Hospital (US), Boston Children's Hospital (US), City Of Hope National Medical Center (US), Children's Hospital of Philadelphia (US), Children's Hospital of Los Angeles (US), Harvard University (US), University of California, San Francisco (US), Dana-Farber Cancer Institute (US), Boston Children's Museum (US), Dana-Farber Brigham Cancer Center (US), Dana-Farber/Boston Children's Cancer and Blood Disorders Center (US), Medical University of Vienna (AT), Stanford University (US)
Openalex Percentile: Top 76%
Glioma Diagnosis and Treatment
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