Non-bioenergetic roles of mitochondrial GPD2 promote tumor progression
Jazyk angličtina Země Austrálie Médium electronic-ecollection
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
36632231
PubMed Central
PMC9830446
DOI
10.7150/thno.75973
PII: thnov13p0438
Knihovny.cz E-zdroje
- Klíčová slova
- DHAP, GPD2, cancer, ether lipids, mitochondria,
- MeSH
- energetický metabolismus MeSH
- ethery metabolismus MeSH
- glycerolfosfátdehydrogenasa * genetika metabolismus MeSH
- lidé MeSH
- mitochondrie * enzymologie MeSH
- myši MeSH
- nádory * enzymologie patologie MeSH
- protoonkogenní proteiny c-akt * metabolismus MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- ethery MeSH
- glycerolfosfátdehydrogenasa * MeSH
- protoonkogenní proteiny c-akt * MeSH
Rationale: Despite growing evidence for mitochondria's involvement in cancer, the roles of specific metabolic components outside the respiratory complex have been little explored. We conducted metabolomic studies on mitochondrial DNA (mtDNA)-deficient (ρ0) cancer cells with lower proliferation rates to clarify the undefined roles of mitochondria in cancer growth. Methods and results: Despite extensive metabolic downregulation, ρ0 cells exhibited high glycerol-3-phosphate (G3P) level, due to low activity of mitochondrial glycerol-3-phosphate dehydrogenase (GPD2). Knockout (KO) of GPD2 resulted in cell growth suppression as well as inhibition of tumor progression in vivo. Surprisingly, this was unrelated to the conventional bioenergetic function of GPD2. Instead, multi-omics results suggested major changes in ether lipid metabolism, for which GPD2 provides dihydroxyacetone phosphate (DHAP) in ether lipid biosynthesis. GPD2 KO cells exhibited significantly lower ether lipid level, and their slower growth was rescued by supplementation of a DHAP precursor or ether lipids. Mechanistically, ether lipid metabolism was associated with Akt pathway, and the downregulation of Akt/mTORC1 pathway due to GPD2 KO was rescued by DHAP supplementation. Conclusion: Overall, the GPD2-ether lipid-Akt axis is newly described for the control of cancer growth. DHAP supply, a non-bioenergetic process, may constitute an important role of mitochondria in cancer.
College of Pharmacy Natural Product Research Institute Seoul National University Seoul 08826 Korea
Faculty of Science Charles University Prague Czech Republic
Institute of Biotechnology Czech Academy of Sciences Prague West Czech Republic
Institute of Physiology Czech Academy of Sciences Prague Czech Republic
School of Pharmacy and Medical Science Griffith University Southport Qld Australia
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