Mitochondrial Protein Density, Biomass, and Bioenergetics as Predictors for the Efficacy of Glioma Treatments

Author:

Sharapova Gulnaz12ORCID,Sabirova Sirina13ORCID,Gomzikova Marina13ORCID,Brichkina Anna14ORCID,Barlev Nick A156,Kalacheva Natalia V2,Rizvanov Albert278ORCID,Markov Nikita9,Simon Hans-Uwe1910

Affiliation:

1. Laboratory of Molecular Immunology, Institute of Fundamental Medicine and Biology, Kazan Federal University, 420008 Kazan, Russia

2. OpenLab Gene and Cell Technology, Institute of Fundamental Medicine and Biology, Kazan Federal University, 420008 Kazan, Russia

3. Laboratory of Intercellular Communication, Kazan Federal University, 420111 Kazan, Russia

4. Institute of Systems Immunology, Center for Tumor Biology and Immunology, Philipps University of Marburg, 35043 Marburg, Germany

5. Gene Expression Program, Institute of Cytology RAS, 194064 Saint-Petersburg, Russia

6. Department of Biomedical Sciences, School of Medicine, Nazarbayev University, Astana 010000, Kazakhstan

7. Division of Medical and Biological Sciences, Tatarstan Academy of Sciences, 420111 Kazan, Russia

8. I.K. Akhunbaev Kyrgyz State Medical Academy, Bishkek 720020, Kyrgyzstan

9. Institute of Pharmacology, University of Bern, 3010 Bern, Switzerland

10. Institute of Biochemistry, Brandenburg Medical School, 16816 Neuruppin, Germany

Abstract

The metabolism of glioma cells exhibits significant heterogeneity and is partially responsible for treatment outcomes. Given this variability, we hypothesized that the effectiveness of treatments targeting various metabolic pathways depends on the bioenergetic profiles and mitochondrial status of glioma cells. To this end, we analyzed mitochondrial biomass, mitochondrial protein density, oxidative phosphorylation (OXPHOS), and glycolysis in a panel of eight glioma cell lines. Our findings revealed considerable variability: mitochondrial biomass varied by up to 3.2-fold, the density of mitochondrial proteins by up to 2.1-fold, and OXPHOS levels by up to 7.3-fold across the cell lines. Subsequently, we stratified glioma cell lines based on their mitochondrial status, OXPHOS, and bioenergetic fitness. Following this stratification, we utilized 16 compounds targeting key bioenergetic, mitochondrial, and related pathways to analyze the associations between induced changes in cell numbers, proliferation, and apoptosis with respect to their steady-state mitochondrial and bioenergetic metrics. Remarkably, a significant fraction of the treatments showed strong correlations with mitochondrial biomass and the density of mitochondrial proteins, suggesting that mitochondrial status may reflect glioma cell sensitivity to specific treatments. Overall, our results indicate that mitochondrial status and bioenergetics are linked to the efficacy of treatments targeting metabolic pathways in glioma.

Funder

Swiss National Science Foundation

Russian Government Program “Recruitment of the Leading Scientists into the Russian Institutions of Higher Education”

Publisher

MDPI AG

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