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Distinct Cholesterol Localization in Glioblastoma Multiforme Revealed by Mass Spectrometry Imaging
[Image: see text] Glioblastoma multiforme (GBM) is the most common and aggressive brain tumor in adults and is highly resistant to chemo- and radiotherapies. GBM has been associated with alterations in lipid contents, but lipid metabolism reprogramming in tumor cells is not fully elucidated. One of...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10161228/ https://www.ncbi.nlm.nih.gov/pubmed/37040529 http://dx.doi.org/10.1021/acschemneuro.2c00776 |
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author | Philipsen, Mai H. Hansson, Ellinor Manaprasertsak, Auraya Lange, Stefan Jennische, Eva Carén, Helena Gatzinsky, Kliment Jakola, Asgeir Hammarlund, Emma U. Malmberg, Per |
author_facet | Philipsen, Mai H. Hansson, Ellinor Manaprasertsak, Auraya Lange, Stefan Jennische, Eva Carén, Helena Gatzinsky, Kliment Jakola, Asgeir Hammarlund, Emma U. Malmberg, Per |
author_sort | Philipsen, Mai H. |
collection | PubMed |
description | [Image: see text] Glioblastoma multiforme (GBM) is the most common and aggressive brain tumor in adults and is highly resistant to chemo- and radiotherapies. GBM has been associated with alterations in lipid contents, but lipid metabolism reprogramming in tumor cells is not fully elucidated. One of the key hurdles is to localize the lipid species that are correlated with tumor growth and invasion. A better understanding of the localization of abnormal lipid metabolism and its vulnerabilities may open up to novel therapeutic approaches. Here, we use time-of-flight secondary ion mass spectrometry (ToF-SIMS) to spatially probe the lipid composition in a GBM biopsy from two regions with different histopathologies: one region with most cells of uniform size and shape, the homogeneous part, and the other with cells showing a great variation in size and shape, the heterogeneous part. Our results reveal elevated levels of cholesterol, diacylglycerols, and some phosphatidylethanolamine in the homogeneous part, while the heterogeneous part was dominated by a variety of fatty acids, phosphatidylcholine, and phosphatidylinositol species. We also observed a high expression of cholesterol in the homogeneous tumor region to be associated with large cells but not with macrophages. Our findings suggest that ToF-SIMS can distinguish in lipid distribution between parts within a human GBM tumor, which can be linked to different molecular mechanisms. |
format | Online Article Text |
id | pubmed-10161228 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-101612282023-05-06 Distinct Cholesterol Localization in Glioblastoma Multiforme Revealed by Mass Spectrometry Imaging Philipsen, Mai H. Hansson, Ellinor Manaprasertsak, Auraya Lange, Stefan Jennische, Eva Carén, Helena Gatzinsky, Kliment Jakola, Asgeir Hammarlund, Emma U. Malmberg, Per ACS Chem Neurosci [Image: see text] Glioblastoma multiforme (GBM) is the most common and aggressive brain tumor in adults and is highly resistant to chemo- and radiotherapies. GBM has been associated with alterations in lipid contents, but lipid metabolism reprogramming in tumor cells is not fully elucidated. One of the key hurdles is to localize the lipid species that are correlated with tumor growth and invasion. A better understanding of the localization of abnormal lipid metabolism and its vulnerabilities may open up to novel therapeutic approaches. Here, we use time-of-flight secondary ion mass spectrometry (ToF-SIMS) to spatially probe the lipid composition in a GBM biopsy from two regions with different histopathologies: one region with most cells of uniform size and shape, the homogeneous part, and the other with cells showing a great variation in size and shape, the heterogeneous part. Our results reveal elevated levels of cholesterol, diacylglycerols, and some phosphatidylethanolamine in the homogeneous part, while the heterogeneous part was dominated by a variety of fatty acids, phosphatidylcholine, and phosphatidylinositol species. We also observed a high expression of cholesterol in the homogeneous tumor region to be associated with large cells but not with macrophages. Our findings suggest that ToF-SIMS can distinguish in lipid distribution between parts within a human GBM tumor, which can be linked to different molecular mechanisms. American Chemical Society 2023-04-11 /pmc/articles/PMC10161228/ /pubmed/37040529 http://dx.doi.org/10.1021/acschemneuro.2c00776 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Philipsen, Mai H. Hansson, Ellinor Manaprasertsak, Auraya Lange, Stefan Jennische, Eva Carén, Helena Gatzinsky, Kliment Jakola, Asgeir Hammarlund, Emma U. Malmberg, Per Distinct Cholesterol Localization in Glioblastoma Multiforme Revealed by Mass Spectrometry Imaging |
title | Distinct Cholesterol
Localization in Glioblastoma
Multiforme Revealed by Mass Spectrometry Imaging |
title_full | Distinct Cholesterol
Localization in Glioblastoma
Multiforme Revealed by Mass Spectrometry Imaging |
title_fullStr | Distinct Cholesterol
Localization in Glioblastoma
Multiforme Revealed by Mass Spectrometry Imaging |
title_full_unstemmed | Distinct Cholesterol
Localization in Glioblastoma
Multiforme Revealed by Mass Spectrometry Imaging |
title_short | Distinct Cholesterol
Localization in Glioblastoma
Multiforme Revealed by Mass Spectrometry Imaging |
title_sort | distinct cholesterol
localization in glioblastoma
multiforme revealed by mass spectrometry imaging |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10161228/ https://www.ncbi.nlm.nih.gov/pubmed/37040529 http://dx.doi.org/10.1021/acschemneuro.2c00776 |
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