Mitochondrial DNA Changes in Respiratory Complex I Genes in Brain Gliomas.
Paulina KozakiewiczLudmiła Grzybowska-SzatkowskaMarzanna CiesielkaPaulina CałkaJacek OsuchowskiPaweł SzmyginBożena JaroszMarta OstrowskaJarosław DudkaAngelika Tkaczyk-WlizłoBrygida ŚlaskaPublished in: Biomedicines (2023)
Mitochondria are organelles necessary for oxidative phosphorylation. The interest in the role of mitochondria in the process of carcinogenesis results from the fact that a respiratory deficit is found in dividing cells, especially in cells with accelerated proliferation. The study included tumor and blood material from 30 patients diagnosed with glioma grade II, III and IV according to WHO (World Health Organization). DNA was isolated from the collected material and next-generation sequencing was performed on the MiSeqFGx apparatus (Illumina). The study searched for a possible relationship between the occurrence of specific mitochondrial DNA polymorphisms in the respiratory complex I genes and brain gliomas of grade II, III and IV. The impact of missense changes on the biochemical properties, structure and functioning of the encoded protein, as well as their potential harmfulness, were assessed in silico along with their belonging to a given mitochondrial subgroup. The A3505G, C3992T, A4024G, T4216C, G5046A, G7444A, T11253C, G12406A and G13604C polymorphisms were assessed as deleterious changes in silico, indicating their association with carcinogenesis.
Keyphrases
- mitochondrial dna
- copy number
- induced apoptosis
- end stage renal disease
- genome wide
- cell cycle arrest
- high grade
- chronic kidney disease
- cell death
- white matter
- molecular docking
- newly diagnosed
- ejection fraction
- resting state
- gene expression
- prognostic factors
- clinical trial
- peritoneal dialysis
- randomized controlled trial
- dna methylation
- brain injury
- autism spectrum disorder
- amino acid
- genome wide analysis
- climate change
- double blind