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Distinct metabolic hallmarks of WHO classified adult glioma subtypes

Björkblom, Benny (författare)
Umeå universitet,Kemiska institutionen
Wibom, Carl (författare)
Umeå universitet,Onkologi
Eriksson, Maria (författare)
Umeå universitet,Onkologi
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Bergenheim, A. Tommy (författare)
Umeå universitet,Neurovetenskaper
Sjöberg, Rickard L. (författare)
Umeå universitet,Neurovetenskaper
Jonsson, Pär (författare)
Umeå universitet,Kemiska institutionen
Brännström, Thomas (författare)
Umeå universitet,Patologi
Antti, Henrik, 1970- (författare)
Umeå universitet,Kemiska institutionen
Sandström, Maria (författare)
Umeå universitet,Onkologi
Melin, Beatrice S. (författare)
Umeå universitet,Onkologi
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 (creator_code:org_t)
2022-02-14
2022
Engelska.
Ingår i: Neuro-Oncology. - : Oxford University Press. - 1522-8517 .- 1523-5866. ; 24:9, s. 1454-1468
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • BACKGROUND: Gliomas are complex tumors with several genetic aberrations and diverse metabolic programs contributing to their aggressive phenotypes and poor prognoses. This study defines key metabolic features that can be used to differentiate between glioma subtypes, with potential for improved diagnostics and subtype targeted therapy.METHODS: Cross-platform global metabolomic profiling coupled with clinical, genetic, and pathological analysis of glioma tissue from 224 tumors - oligodendroglioma (n=31), astrocytoma (n=31) and glioblastoma (n=162) - were performed. Identified metabolic phenotypes were evaluated in accordance with the WHO classification, IDH-mutation, 1p/19q-codeletion, WHO-grading 2-4, and MGMT promoter methylation.RESULTS: Distinct metabolic phenotypes separate all six analyzed glioma subtypes. IDH-mutated subtypes, expressing 2-hydroxyglutaric acid, were clearly distinguished from IDH-wildtype subtypes. Considerable metabolic heterogeneity outside of the mutated IDH pathway were also evident, with key metabolites being high expression of glycerophosphates, inositols, monosaccharides and sugar alcohols and low levels of sphingosine and lysoglycerophospholipids in IDH-mutants. Among the IDH-mutated subtypes, we observed high levels of amino acids, especially glycine and 2-aminoadipic acid, in grade 4 glioma, and N-acetyl aspartic acid in low-grade astrocytoma and oligodendroglioma. Both IDH-wildtype and mutated oligodendroglioma and glioblastoma were characterized by high levels of acylcarnitines, likely driven by rapid cell growth and hypoxic features. We found elevated levels of 5-HIAA in gliosarcoma and a subtype of oligodendroglioma not yet defined as a specific entity, indicating a previously not described role for the serotonin pathway linked to glioma with bimorphic tissue.CONCLUSION: Key metabolic differences exist across adult glioma subtypes.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Nyckelord

Astrocytoma
Glioblastoma
Metabolic reprogramming
Oligodendroglioma
WHO classification
molekylärbiologi
Molecular Biology
Pathology
patologi
Oncology
onkologi

Publikations- och innehållstyp

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