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Excessive lipid production shapes glioma tumor microenvironment.
Maraqah, Haitham H; Aboubechara, John Paul; Abu-Asab, Mones S; Lee, Han Sung; Aboud, Orwa.
  • Maraqah HH; Medicine & Health Science Faculty, School of Meidicine, An-Najah National University, Nablus, Palestine.
  • Aboubechara JP; Department of Neurology, University of California Davis, Sacramento, CA, USA.
  • Abu-Asab MS; Comprehensive Cancer Center, University of California, Davis, Sacramento, CA, USA.
  • Lee HS; Electron Microscopy Lab, Biological Imaging Core, National Eye Institute, National Institutes of Health, Bethesda, MD, USA.
  • Aboud O; Department of Pathology and Laboratory Medicine, UC Davis Comprehensive Cancer Center, University of California Davis, Sacramento, CA, USA.
Ultrastruct Pathol ; 48(5): 367-377, 2024 Sep 02.
Article en En | MEDLINE | ID: mdl-39157967
ABSTRACT
Disrupted lipid metabolism is a characteristic of gliomas. This study utilizes an ultrastructural approach to characterize the prevalence and distribution of lipids within gliomas. This study made use of tissue from IDH1 wild type (IDH1-wt) glioblastoma (n = 18) and IDH1 mutant (IDH1-mt) astrocytoma (n = 12) tumors. We uncover a prevalent and intriguing surplus of lipids. The bulk of the lipids manifested as sizable cytoplasmic inclusions and extracellular deposits in the tumor microenvironment (TME); in some tumors the lipids were stored in the classical membraneless spheroidal lipid droplets (LDs). Frequently, lipids accumulated inside mitochondria, suggesting possible dysfunction of the beta-oxidation pathway. Additionally, the tumor vasculature have lipid deposits in their lumen and vessel walls; this lipid could have shifted in from the tumor microenvironment or have been produced by the vessel-invading tumor cells. Lipid excess in gliomas stems from disrupted beta-oxidation and dysfunctional oxidative phosphorylation pathways. The implications of this lipid-driven environment include structural support for the tumor cells and protection against immune responses, non-lipophilic drugs, and free radicals.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / Metabolismo de los Lípidos / Microambiente Tumoral / Glioma Límite: Female / Humans / Male / Middle aged Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / Metabolismo de los Lípidos / Microambiente Tumoral / Glioma Límite: Female / Humans / Male / Middle aged Idioma: En Año: 2024 Tipo del documento: Article