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OTEH-7. Molecular characterization of tumor stiffness in glioblastoma

Tumor heterogeneity is one of the hallmarks of glioblastoma multiforme (GBM). Morphology within a given GBM tumor can be extremely variable where some regions of the tumor have a soft, gel-like structure while other areas are dense and fibrous. Abnormal mechanical stress and tissue stiffening caused...

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Autores principales: Halldorsson, Skarphedinn, Svensson, Siri Fløgstad, Berg, Henriette Engen, Wolrab, Denise, Rise, Frode, Wilkins, Alistair, Wilson, Steven Ray, Holcapek, Michal, Emblem, Kyrre Eeg, Vik-Mo, Einar O
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8255452/
http://dx.doi.org/10.1093/noajnl/vdab070.046
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author Halldorsson, Skarphedinn
Svensson, Siri Fløgstad
Berg, Henriette Engen
Wolrab, Denise
Rise, Frode
Wilkins, Alistair
Wilson, Steven Ray
Holcapek, Michal
Emblem, Kyrre Eeg
Vik-Mo, Einar O
author_facet Halldorsson, Skarphedinn
Svensson, Siri Fløgstad
Berg, Henriette Engen
Wolrab, Denise
Rise, Frode
Wilkins, Alistair
Wilson, Steven Ray
Holcapek, Michal
Emblem, Kyrre Eeg
Vik-Mo, Einar O
author_sort Halldorsson, Skarphedinn
collection PubMed
description Tumor heterogeneity is one of the hallmarks of glioblastoma multiforme (GBM). Morphology within a given GBM tumor can be extremely variable where some regions of the tumor have a soft, gel-like structure while other areas are dense and fibrous. Abnormal mechanical stress and tissue stiffening caused by cancer proliferation are believed to affect vascularity by compressing structurally weak blood vessels and restricting the supply of nutrients and oxygen to the tissue. These effects contribute to a hypoxic microenvironment that promotes disease progression and chemoresistance. The genetic and molecular mechanisms that govern tissue stiffness within GBM tumors, however, are largely unknown. Magnetic Resonance Elastography (MRE) is an emerging technique for quantifying tissue stiffness non-invasively. We have evaluated 10 GBM patients by MRE imaging obtained prior to surgical resection. During surgery, 2–7 stereotactically navigated biopsies were collected from locations within the tumor with varying degrees of measured stiffness. Biopsies were processed to extract RNA, proteins, polar metabolites and lipids. Biomolecules were analyzed on relevant -omics platforms (RNA sequencing, MS-proteomics and lipidomics, NMR of polar metabolites). Differential expression and gene set enrichment analysis of patient paired biopsies indicate an overall increase in macrophage infiltration and extracellular matrix re-organization associated with increased tumor stiffness. Among the most highly upregulated genes in stiff tumor tissue were lymphatic endothelial hyaluronic acid receptor 1 (LYVE-1) and macrophage receptor with collagenous structure (MARCO), both of which have been associated with immune cell infiltration and tissue stiffness. Our preliminary findings offer novel insights into tumor morphology in GBM that can be inferred from imaging prior to surgery. This can be used to identify tumor regions with high risk of progression and infiltration, thereby informing and guiding surgical strategy and may ultimately lead to novel treatment strategies.
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spelling pubmed-82554522021-07-06 OTEH-7. Molecular characterization of tumor stiffness in glioblastoma Halldorsson, Skarphedinn Svensson, Siri Fløgstad Berg, Henriette Engen Wolrab, Denise Rise, Frode Wilkins, Alistair Wilson, Steven Ray Holcapek, Michal Emblem, Kyrre Eeg Vik-Mo, Einar O Neurooncol Adv Supplement Abstracts Tumor heterogeneity is one of the hallmarks of glioblastoma multiforme (GBM). Morphology within a given GBM tumor can be extremely variable where some regions of the tumor have a soft, gel-like structure while other areas are dense and fibrous. Abnormal mechanical stress and tissue stiffening caused by cancer proliferation are believed to affect vascularity by compressing structurally weak blood vessels and restricting the supply of nutrients and oxygen to the tissue. These effects contribute to a hypoxic microenvironment that promotes disease progression and chemoresistance. The genetic and molecular mechanisms that govern tissue stiffness within GBM tumors, however, are largely unknown. Magnetic Resonance Elastography (MRE) is an emerging technique for quantifying tissue stiffness non-invasively. We have evaluated 10 GBM patients by MRE imaging obtained prior to surgical resection. During surgery, 2–7 stereotactically navigated biopsies were collected from locations within the tumor with varying degrees of measured stiffness. Biopsies were processed to extract RNA, proteins, polar metabolites and lipids. Biomolecules were analyzed on relevant -omics platforms (RNA sequencing, MS-proteomics and lipidomics, NMR of polar metabolites). Differential expression and gene set enrichment analysis of patient paired biopsies indicate an overall increase in macrophage infiltration and extracellular matrix re-organization associated with increased tumor stiffness. Among the most highly upregulated genes in stiff tumor tissue were lymphatic endothelial hyaluronic acid receptor 1 (LYVE-1) and macrophage receptor with collagenous structure (MARCO), both of which have been associated with immune cell infiltration and tissue stiffness. Our preliminary findings offer novel insights into tumor morphology in GBM that can be inferred from imaging prior to surgery. This can be used to identify tumor regions with high risk of progression and infiltration, thereby informing and guiding surgical strategy and may ultimately lead to novel treatment strategies. Oxford University Press 2021-07-05 /pmc/articles/PMC8255452/ http://dx.doi.org/10.1093/noajnl/vdab070.046 Text en © The Author(s) 2021. Published by Oxford University Press, the Society for Neuro-Oncology and the European Association of Neuro-Oncology. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Supplement Abstracts
Halldorsson, Skarphedinn
Svensson, Siri Fløgstad
Berg, Henriette Engen
Wolrab, Denise
Rise, Frode
Wilkins, Alistair
Wilson, Steven Ray
Holcapek, Michal
Emblem, Kyrre Eeg
Vik-Mo, Einar O
OTEH-7. Molecular characterization of tumor stiffness in glioblastoma
title OTEH-7. Molecular characterization of tumor stiffness in glioblastoma
title_full OTEH-7. Molecular characterization of tumor stiffness in glioblastoma
title_fullStr OTEH-7. Molecular characterization of tumor stiffness in glioblastoma
title_full_unstemmed OTEH-7. Molecular characterization of tumor stiffness in glioblastoma
title_short OTEH-7. Molecular characterization of tumor stiffness in glioblastoma
title_sort oteh-7. molecular characterization of tumor stiffness in glioblastoma
topic Supplement Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8255452/
http://dx.doi.org/10.1093/noajnl/vdab070.046
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