Evidence map›Paper›PMID 37040529›Full record

ArticleACS chemical neuroscience2023

Distinct Cholesterol Localization in Glioblastoma Multiforme Revealed by Mass Spectrometry Imaging.

Mai H Philipsen, Ellinor Hansson, Auraya Manaprasertsak, Stefan Lange, Eva Jennische, Helena Carén, Kliment Gatzinsky, Asgeir Jakola, Emma U Hammarlund, Per Malmberg

Open access · hybridAbstract read
In one paragraph

Article in ACS chemical neuroscience, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
3.3field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 14 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 1 country.

Mai H PhilipsenTissue Development and Evolution (TiDE) Division, Department of Laboratory Medicine, Lund University, SE22100 Lund, Sweden.
Ellinor HanssonDepartment of Chemistry and Chemical Engineering, Chalmers University of Technology, SE41296 Gothenburg, Sweden.
Auraya ManaprasertsakTissue Development and Evolution (TiDE) Division, Department of Laboratory Medicine, Lund University, SE22100 Lund, Sweden.
Stefan LangeInstitute of Biomedicine, University of Gothenburg, SE41390 Gothenburg, Sweden.
Eva JennischeInstitute of Biomedicine, University of Gothenburg, SE41390 Gothenburg, Sweden.ORCID 0000-0002-2147-8412
Helena CarénSahlgrenska Centre for Cancer Research, Department of Medical Biochemistry and Cell biology, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, SE41390 Gothenburg, Sweden.
Kliment GatzinskyDepartment of Neurosurgery, Sahlgrenska University Hospital, SE41345 Gothenburg, Sweden.
Asgeir JakolaDepartment of Neurosurgery, Sahlgrenska University Hospital, SE41345 Gothenburg, Sweden.
Emma U HammarlundTissue Development and Evolution (TiDE) Division, Department of Laboratory Medicine, Lund University, SE22100 Lund, Sweden.
Per MalmbergDepartment of Chemistry and Chemical Engineering, Chalmers University of Technology, SE41296 Gothenburg, Sweden.ORCID 0000-0002-6487-7851
Lund University · SEUniversity of Gothenburg · SEChalmers University of Technology · SESahlgrenska University Hospital · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

CholesterolGlioblastomaBiopsyHumansSpectrometry, Mass, Secondary IonCholesterolcholesterolglioblastomalipidsmass spectrometry imaging

Identifiers

PMID37040529
PMCPMC10161228
OpenAlexW4364377756

What Socratic holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.