Evidence map›Paper›PMID 42364223›Full record

ArticleThe Eurasian journal of medicine2026

Mitochondrial DNA Content Modulates Chemosensitivity and Cellular Adaptation in Glioblastoma Cells.

Siti Muslihah Ab Radzak, Azim Patar, Hsin-Chen Lee, Abdul Aziz Mohamed Yusoff

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Article in The Eurasian journal of medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Siti Muslihah Ab RadzakDepartment of Neurosciences, School of Medical Sciences, Universiti Sains Malaysia, Health Campus, Kubang Kerian, Kelantan, Malaysia.
Azim PatarDepartment of Neurosciences, School of Medical Sciences, Universiti Sains Malaysia, Health Campus, Kubang Kerian, Kelantan, Malaysia.
Hsin-Chen LeeDepartment and Institute of Pharmacology, National Yang-Ming Chiao-Tung University College of Medicine, Taipei, Taiwan.
Abdul Aziz Mohamed YusoffDepartment of Neurosciences, School of Medical Sciences, Universiti Sains Malaysia, Health Campus, Kubang Kerian, Kelantan, Malaysia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMitochondrial DNA (mtDNA) copy number alterations are closely associated with glioblastoma (GBM) progression and therapeutic resistance. This study investigates how changes in mitochondrial content affect the chemotherapeutic response of GBM cells in vitro.

methodsGlioblastoma cell lines (U87 and LN18) were initially treated with ethidium bromide (EtBr) to deplete mtDNA, followed by EtBr withdrawal to enable mtDNA restoration. Real-time Polymerase Chain Reaction (PCR) was subsequently employed to quantify mtDNA levels. To assess cellular responses, cell viability was measured using the CCK-8 assay, while wound healing and Transwell assays were conducted to evaluate cell migration and invasion. Apoptosis was analyzed via flow cytometry using the Annexin V-FITC/ PI kit. In addition, intracellular reactive oxygen species (ROS) and mitochondrial membrane potential (ΔΨm) were examined by flow cytometry, and Adenosine triphosphate (ATP) levels were quantified using a luminescent ATP detection assay.

resultsGlioblastoma cells with depleted mtDNA exhibited an increase in mtDNA content following temozolomide (TMZ) exposure. Despite this, these cells showed reduced viability, migration, and invasion, while also displaying adaptive responses suggestive of emerging resistance. In contrast, cells in which mtDNA content had been restored demonstrated recovery across all parameters, indicating enhanced sensitivity to TMZ.

conclusionThis study highlights the essential role of mtDNA content in modulating GBM cell sensitivity to chemotherapy, as variations in mtDNA levels can influence cellular responses to treatment. These findings suggest that mtDNA content could act as a potential biomarker and that its modulation may offer a promising strategy to overcome drug resistance in GBM. Cite this article as: Radzak SMA, Patar A, Lee H, Yusoff AAM. Mitochondrial DNA content modulates chemosensitivity and cellular adaptation in glioblastoma cells. Eurasian J Med. 2026, 58(2), 1207, doi: 10.5152/eurasianjmed.2026.251207.

Identifiers

PMID42364223
PMCPMC13185615

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