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Upregulation of energy metabolism-related, p53-target TIGAR and SCO2 in HuH-7 cells with p53 mutation by geranylgeranoic acid treatment.
Biomed Res. 2015; 36(6):371-81.BR

Abstract

Metabolic alternation in cancer cells is one of the most common characteristics that distinguish malignant cells from normal cells. Many studies have explained the Warburg hypothesis that cancer cells obtain more energy from aerobic glycolysis than mitochondrial respiration. Here, we show that a branched-chain C-20 polyunsaturated fatty acid, geranylgeranoic acid (GGA), induces upregulation of the cellular protein levels of TP53-induced glycolysis and apoptosis regulator (TIGAR) and synthesis of cytochrome c oxidase 2 (SCO2) in human hepatoma-derived HuH-7cells harboring the mutant TP53 gene, suggesting that GGA may shift an energetic state of the tumor cells from aerobic glycolysis to mitochondrial respiration. In addition, UPLC/TOF/MS-based metabolomics analysis supported the GGA-induced energetic shift, as it revealed that GGA induced a time-dependent increase in the cellular contents of fructose 6-phosphate and decrease of fructose 1,6-diphosphate. Furthermore, metabolomics analysis revealed that GGA rapidly induced spermine accumulation with slight decrease of spermidine. Taken together, the present study strongly suggests that GGA may shift HuH-7 cells from aerobic glycolysis to mitochondrial respiration through the immediate upregulation of TIGAR and SCO2 protein levels.

Authors+Show Affiliations

Molecular and Cellular Biology, Graduate School of Human Health Science, University of Nagasaki.No affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

26700591

Citation

Iwao, Chieko, and Yoshihiro Shidoji. "Upregulation of Energy Metabolism-related, P53-target TIGAR and SCO2 in HuH-7 Cells With P53 Mutation By Geranylgeranoic Acid Treatment." Biomedical Research (Tokyo, Japan), vol. 36, no. 6, 2015, pp. 371-81.
Iwao C, Shidoji Y. Upregulation of energy metabolism-related, p53-target TIGAR and SCO2 in HuH-7 cells with p53 mutation by geranylgeranoic acid treatment. Biomed Res. 2015;36(6):371-81.
Iwao, C., & Shidoji, Y. (2015). Upregulation of energy metabolism-related, p53-target TIGAR and SCO2 in HuH-7 cells with p53 mutation by geranylgeranoic acid treatment. Biomedical Research (Tokyo, Japan), 36(6), 371-81. https://doi.org/10.2220/biomedres.36.371
Iwao C, Shidoji Y. Upregulation of Energy Metabolism-related, P53-target TIGAR and SCO2 in HuH-7 Cells With P53 Mutation By Geranylgeranoic Acid Treatment. Biomed Res. 2015;36(6):371-81. PubMed PMID: 26700591.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Upregulation of energy metabolism-related, p53-target TIGAR and SCO2 in HuH-7 cells with p53 mutation by geranylgeranoic acid treatment. AU - Iwao,Chieko, AU - Shidoji,Yoshihiro, PY - 2015/12/25/entrez PY - 2015/12/25/pubmed PY - 2016/9/23/medline SP - 371 EP - 81 JF - Biomedical research (Tokyo, Japan) JO - Biomed Res VL - 36 IS - 6 N2 - Metabolic alternation in cancer cells is one of the most common characteristics that distinguish malignant cells from normal cells. Many studies have explained the Warburg hypothesis that cancer cells obtain more energy from aerobic glycolysis than mitochondrial respiration. Here, we show that a branched-chain C-20 polyunsaturated fatty acid, geranylgeranoic acid (GGA), induces upregulation of the cellular protein levels of TP53-induced glycolysis and apoptosis regulator (TIGAR) and synthesis of cytochrome c oxidase 2 (SCO2) in human hepatoma-derived HuH-7cells harboring the mutant TP53 gene, suggesting that GGA may shift an energetic state of the tumor cells from aerobic glycolysis to mitochondrial respiration. In addition, UPLC/TOF/MS-based metabolomics analysis supported the GGA-induced energetic shift, as it revealed that GGA induced a time-dependent increase in the cellular contents of fructose 6-phosphate and decrease of fructose 1,6-diphosphate. Furthermore, metabolomics analysis revealed that GGA rapidly induced spermine accumulation with slight decrease of spermidine. Taken together, the present study strongly suggests that GGA may shift HuH-7 cells from aerobic glycolysis to mitochondrial respiration through the immediate upregulation of TIGAR and SCO2 protein levels. SN - 1880-313X UR - https://www.unboundmedicine.com/medline/citation/26700591/Upregulation_of_energy_metabolism_related_p53_target_TIGAR_and_SCO2_in_HuH_7_cells_with_p53_mutation_by_geranylgeranoic_acid_treatment_ L2 - https://dx.doi.org/10.2220/biomedres.36.371 DB - PRIME DP - Unbound Medicine ER -