Mitochondrial DNA copy number changes, heteroplasmy, and mutations in plasma-derived exosomes and brain tissue of glioblastoma patients

• Published in: Molecular and cellular probes Vol. 66; p. 101875
• Main Authors: Soltész, Beáta, Pös, Ondrej, Wlachovska, Zuzana, Budis, Jaroslav, Hekel, Rastislav, Strieskova, Lucia, Liptak, Jana Bozenka, Krampl, Werner, Styk, Jakub, Németh, Nikolett, Keserű, Judit Sz, Jenei, Adrienn, Buglyó, Gergely, Klekner, Álmos, Nagy, Bálint, Szemes, Tomas
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 01.12.2022
• Subjects: Adult; Brain; Copy number; DNA Copy Number Variations - genetics; DNA, Mitochondrial - analysis; DNA, Mitochondrial - genetics; Exosome; Exosomes - genetics; Glioblastoma; Glioblastoma - genetics; Heteroplasmy; Humans; Mitochondria - genetics; Mitochondrial DNA; Mutation - genetics; Mutations; Mutations; Mitochondrial DNA; Exosome; Copy number; Heteroplasmy; Glioblastoma
• ISSN: 0890-8508; 1096-1194
• DOI: 10.1016/j.mcp.2022.101875

Glioblastoma is the most common malignant tumor of the central nervous system (CNS) in adults. Glioblastoma cells show increased glucose consumption associated with poor prognosis. Since mitochondria play a crucial role in energy metabolism, mutations and copy number changes of mitochondrial DNA may serve as biomarkers. As the brain is difficult to access, analysis of mitochondria directly from the brain tissue represents a challenge. Exosome analysis is an alternative (still poorly explored) approach to investigate molecular changes in CNS tumors. We analyzed brain tissue DNA and plasma-derived exosomal DNA (exoDNA) of 44 glioblastoma patients and 40 control individuals. Quantitative real-time PCR was performed to determine mtDNA copy numbers and the Kruskal-Wallis and Mann-Whitney U test were used for statistical analysis of data. Subsequently, sequencing libraries were prepared and sequenced on the MiSeq platform to identify mtDNA point mutations. Tissue mtDNA copy number was different among controls and patients in multiple comparisons. A similar tendency was detected in exosomes. Based on NGS analysis, several mtDNA point mutations showed slightly different frequencies between cases and controls, but the clinical relevance of these observations is difficult to assess and likely less than that of overall mtDNA copy number changes. Allele frequencies of variants were used to determine the level of heteroplasmy (found to be higher in exo-mtDNA of control individuals). Despite the suggested potential, the use of such biomarkers for the screening and/or diagnosis of glioblastomas is still limited, thus further studies are needed. •An original research paper on mitochondrial DNA copy number changes, heteroplasmy, and mutations in plasma-derived exosomes and brain tissue of glioblastoma patients.•Higher mtDNA copy numbers were observed in controls than in glioblastoma cases in both samples (brain tissue and plasma-derived exosomes), suggesting the liquid biopsy specimens might also be good source of determination of mtDNA copy number.•Several mtDNA point mutations showed slightly different frequencies between cases and controls.•Plasma-derived exoDNA might be a more suitable source to capture the spectrum of heteroplasmic variations on the intercellular level.