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dc.contributor.authorBjørnetrø, Tonje
dc.contributor.authorBousquet, Paula
dc.contributor.authorRedalen, Kathrine Røe
dc.contributor.authorSiebke, Anne-Marie
dc.contributor.authorLüders, Torben
dc.contributor.authorStang, Espen
dc.contributor.authorSanabria-Moreno, Adriana Maria
dc.contributor.authorJohansen, Christin
dc.contributor.authorFuglestad, Anniken Jørlo
dc.contributor.authorKersten, Christian
dc.contributor.authorMeltzer, Sebastian
dc.contributor.authorRee, Anne Hansen
dc.date.accessioned2023-11-09T12:56:27Z
dc.date.available2023-11-09T12:56:27Z
dc.date.created2023-07-25T11:26:47Z
dc.date.issued2023
dc.identifier.citationBMC Cancer. 2023, 23 (1), 650-?.en_US
dc.identifier.issn1471-2407
dc.identifier.urihttps://hdl.handle.net/11250/3101670
dc.description.abstractBackground Recent reports have demonstrated that the entire mitochondrial genome can be secreted in extracellular vesicles (EVs), but the biological attributes of this cell-free mitochondrial DNA (mtDNA) remain insufficiently understood. We used next-generation sequencing to compare plasma EV-derived mtDNA to that of whole blood (WB), peripheral blood mononuclear cells (PBMCs), and formalin-fixed paraffin-embedded (FFPE) tumor tissue from eight rectal cancer patients and WB and fresh-frozen (FF) tumor tissue from eight colon cancer patients. Methods Total DNA was isolated before the mtDNA was enriched by PCR with either two primer sets generating two long products or multiple primer sets (for the FFPE tumors), prior to the sequencing. mtDNA diversity was assessed as the total variant number, level of heteroplasmy (mutant mtDNA copies mixed with wild-type copies), variant distribution within the protein-coding genes, and the predicted functional effect of the variants in the different sample types. Differences between groups were compared by paired Student’s t-test or ANOVA with Dunnett’s multiple comparison tests when comparing matched samples from patients. Mann–Whitney U test was used when comparing differences between the cancer types and patient groups. Pearson correlation analysis was performed. Results In both cancer types, EV mtDNA presented twice as many variants and had significantly more low-level heteroplasmy than WB mtDNA. The EV mtDNA variants were clustered in the coding regions, and the proportion of EV mtDNA variants that were missense mutations (i.e., estimated to moderately affect the mitochondrial protein function) was significantly higher than in WB and tumor tissues. Nonsense mutations (i.e., estimated to highly affect the mitochondrial protein function) were only observed in the tumor tissues and EVs. Conclusion Taken together, plasma EV mtDNA in CRC patients exhibits a high degree of diversity.en_US
dc.language.isoengen_US
dc.publisherBMCen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleNext-generation sequencing reveals mitogenome diversity in plasma extracellular vesicles from colorectal cancer patientsen_US
dc.title.alternativeNext-generation sequencing reveals mitogenome diversity in plasma extracellular vesicles from colorectal cancer patientsen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.pagenumber650-?en_US
dc.source.volume23en_US
dc.source.journalBMC Canceren_US
dc.source.issue1en_US
dc.identifier.doi10.1186/s12885-023-11092-x
dc.identifier.cristin2163427
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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