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Spatial cellular architecture predicts prognosis in glioblastoma

Intra-tumoral heterogeneity and cell-state plasticity are key drivers for the therapeutic resistance of glioblastoma. Here, we investigate the association between spatial cellular organization and glioblastoma prognosis. Leveraging single-cell RNA-seq and spatial transcriptomics data, we develop a d...

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Autores principales: Zheng, Yuanning, Carrillo-Perez, Francisco, Pizurica, Marija, Heiland, Dieter Henrik, Gevaert, Olivier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10336135/
https://www.ncbi.nlm.nih.gov/pubmed/37433817
http://dx.doi.org/10.1038/s41467-023-39933-0
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author Zheng, Yuanning
Carrillo-Perez, Francisco
Pizurica, Marija
Heiland, Dieter Henrik
Gevaert, Olivier
author_facet Zheng, Yuanning
Carrillo-Perez, Francisco
Pizurica, Marija
Heiland, Dieter Henrik
Gevaert, Olivier
author_sort Zheng, Yuanning
collection PubMed
description Intra-tumoral heterogeneity and cell-state plasticity are key drivers for the therapeutic resistance of glioblastoma. Here, we investigate the association between spatial cellular organization and glioblastoma prognosis. Leveraging single-cell RNA-seq and spatial transcriptomics data, we develop a deep learning model to predict transcriptional subtypes of glioblastoma cells from histology images. Employing this model, we phenotypically analyze 40 million tissue spots from 410 patients and identify consistent associations between tumor architecture and prognosis across two independent cohorts. Patients with poor prognosis exhibit higher proportions of tumor cells expressing a hypoxia-induced transcriptional program. Furthermore, a clustering pattern of astrocyte-like tumor cells is associated with worse prognosis, while dispersion and connection of the astrocytes with other transcriptional subtypes correlate with decreased risk. To validate these results, we develop a separate deep learning model that utilizes histology images to predict prognosis. Applying this model to spatial transcriptomics data reveal survival-associated regional gene expression programs. Overall, our study presents a scalable approach to unravel the transcriptional heterogeneity of glioblastoma and establishes a critical connection between spatial cellular architecture and clinical outcomes.
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spelling pubmed-103361352023-07-13 Spatial cellular architecture predicts prognosis in glioblastoma Zheng, Yuanning Carrillo-Perez, Francisco Pizurica, Marija Heiland, Dieter Henrik Gevaert, Olivier Nat Commun Article Intra-tumoral heterogeneity and cell-state plasticity are key drivers for the therapeutic resistance of glioblastoma. Here, we investigate the association between spatial cellular organization and glioblastoma prognosis. Leveraging single-cell RNA-seq and spatial transcriptomics data, we develop a deep learning model to predict transcriptional subtypes of glioblastoma cells from histology images. Employing this model, we phenotypically analyze 40 million tissue spots from 410 patients and identify consistent associations between tumor architecture and prognosis across two independent cohorts. Patients with poor prognosis exhibit higher proportions of tumor cells expressing a hypoxia-induced transcriptional program. Furthermore, a clustering pattern of astrocyte-like tumor cells is associated with worse prognosis, while dispersion and connection of the astrocytes with other transcriptional subtypes correlate with decreased risk. To validate these results, we develop a separate deep learning model that utilizes histology images to predict prognosis. Applying this model to spatial transcriptomics data reveal survival-associated regional gene expression programs. Overall, our study presents a scalable approach to unravel the transcriptional heterogeneity of glioblastoma and establishes a critical connection between spatial cellular architecture and clinical outcomes. Nature Publishing Group UK 2023-07-11 /pmc/articles/PMC10336135/ /pubmed/37433817 http://dx.doi.org/10.1038/s41467-023-39933-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Zheng, Yuanning
Carrillo-Perez, Francisco
Pizurica, Marija
Heiland, Dieter Henrik
Gevaert, Olivier
Spatial cellular architecture predicts prognosis in glioblastoma
title Spatial cellular architecture predicts prognosis in glioblastoma
title_full Spatial cellular architecture predicts prognosis in glioblastoma
title_fullStr Spatial cellular architecture predicts prognosis in glioblastoma
title_full_unstemmed Spatial cellular architecture predicts prognosis in glioblastoma
title_short Spatial cellular architecture predicts prognosis in glioblastoma
title_sort spatial cellular architecture predicts prognosis in glioblastoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10336135/
https://www.ncbi.nlm.nih.gov/pubmed/37433817
http://dx.doi.org/10.1038/s41467-023-39933-0
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