Mitochondria transfer in Glioblastoma

Glioblastoma (GBM) is a highly aggressive and metabolically adaptable brain tumor characterized by profound cellular heterogeneity and therapy resistance. Recent research has uncovered the phenomenon of horizontal mitochondrial transfer (HMT) between GBM cells and their microenvironment, particularly astrocytes, which contributes to tumor progression, metabolic reprogramming, and treatment resistance. This review summarises current knowledge on mitochondrial exchange in GBM via tunneling nanotubes (TNTs), tumor microtubes (TMs) and potentially via extracellular vesicles (EVs). It also explores the functional consequences of HMT, including enhanced oxidative phosphorylation (OXPHOS), increased tumorigenicity, and altered therapeutic responses. This review highlights the need for further investigation into the molecular drivers and context-specific outcomes of mitochondrial transfer in GBM, with implications for novel therapeutic strategies.

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Publication Details

Journal
Neuro-Oncology
Published
2026-02-21
DOI
https://doi.org/10.1093/neuonc/noag038
Primary Topic
Mitochondrial Function and Pathology
Type
article
Field-Weighted Citation Impact
0.00
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Mitochondria transfer in Glioblastoma

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Mitochondria transfer in Glioblastoma

Dionysios Christos Watson, Justin Durla Lathia, Simon Storevik, Hrvoje Miletić, Nikhil Panicker, Mina Thue Augustsson, Amanda M Serapiglia, Carolina De La Pena Fernandez, Shannon Moreino, Defne Bayik, Hanjo Köppe
article en

Abstract

Glioblastoma (GBM) is a highly aggressive and metabolically adaptable brain tumor characterized by profound cellular heterogeneity and therapy resistance. Recent research has uncovered the phenomenon of horizontal mitochondrial transfer (HMT) between GBM cells and their microenvironment, particularly astrocytes, which contributes to tumor progression, metabolic reprogramming, and treatment resistance. This review summarises current knowledge on mitochondrial exchange in GBM via tunneling nanotubes (TNTs), tumor microtubes (TMs) and potentially via extracellular vesicles (EVs). It also explores the functional consequences of HMT, including enhanced oxidative phosphorylation (OXPHOS), increased tumorigenicity, and altered therapeutic responses. This review highlights the need for further investigation into the molecular drivers and context-specific outcomes of mitochondrial transfer in GBM, with implications for novel therapeutic strategies.

Neuro-Oncology
University of Copenhagen (DK), Cleveland Clinic (US), University of Miami (US), Universitätsmedizin Greifswald (DE), Haukeland University Hospital (NO), Universität Greifswald (DE), University of Bergen (NO), Case Western Reserve University (US)
Good health and well-being
Openalex Percentile: Top 45%
Mitochondrial Function and Pathology
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