All Three AKT Isoforms Can Upregulate Oxygen Metabolism and Lactate Production in Human Hepatocellular Carcinoma Cell Lines

• Published in: International journal of molecular sciences 2024-02, Vol.25 (4), p.2168
• Main Authors: Tian, Ling-Yu, Smit, Daniel J, Popova, Nadezhda V, Horn, Stefan, Velasquez, Lis Noelia, Huber, Samuel, Jücker, Manfred
• Format: Article
• Language: English
• Subjects: Acidification; AKT isoforms; AKT signaling; Aprotinin; Carcinoma, Hepatocellular - genetics; Carcinoma, Hepatocellular - metabolism; Cell Line, Tumor; Cells; Dehydrogenases; Ethylenediaminetetraacetic acid; extracellular acidification; Glucose; glycolysis; Hepatoma; Homeostasis; Humans; Instrument industry; Kinases; lactate metabolism; Lactic Acid - metabolism; Liver cancer; Liver diseases; Liver Neoplasms - genetics; Liver Neoplasms - metabolism; Medical prognosis; Metabolism; Metabolites; Oxidoreductases; Oxygen - metabolism; Phosphatidylinositol 3-Kinases; Phosphorylation; Protein Isoforms - genetics; Protein Isoforms - metabolism; Proto-Oncogene Proteins c-akt - metabolism; Pyruvates; Respiration; Scientific equipment and supplies industry; Signal transduction; Tumors
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms25042168

Hepatocellular carcinoma (HCC), the main pathological type of liver cancer, is related to risk factors such as viral hepatitis, alcohol intake, and non-alcoholic fatty liver disease (NAFLD). The constitutive activation of the PI3K/AKT signaling pathway is common in HCC and has essential involvement in tumor progression. The serine/threonine kinase AKT has several downstream substrates, which have been implicated in the regulation of cellular metabolism. However, the contribution of each of the three AKT isoforms, i.e., AKT1, AKT2 and AKT3, to HCC metabolism has not been comprehensively investigated. In this study, we analyzed the functional role of AKT1, AKT2 and AKT3 in HCC metabolism. The overexpression of activated AKT1, AKT2 and AKT3 isoforms in the human HCC cell lines Hep3B and Huh7 resulted in higher oxygen consumption rate (OCR), ATP production, maximal respiration and spare respiratory capacity in comparison to vector-transduced cells. Vice versa, lentiviral vector-mediated knockdowns of each AKT isoform reduced OCR in both cell lines. Reduced OCR rates observed in the three AKT isoform knockdowns were associated with reduced extracellular acidification rates (ECAR) and reduced lactate production in both analyzed cell lines. Mechanistically, the downregulation of OCR by AKT isoform knockdowns correlated with an increased phosphorylation of the pyruvate dehydrogenase on Ser232, which negatively regulates the activity of this crucial gatekeeper of mitochondrial respiration. In summary, our data indicate that each of the three AKT isoforms is able to upregulate OCR, ECAR and lactate production independently of each other in human HCC cells through the regulation of the pyruvate dehydrogenase.