ATP Production Relies on Fatty Acid Oxidation Rather than Glycolysis in Pancreatic Ductal Adenocarcinoma

• Published in: Cancers Vol. 12; no. 9; p. 2477
• Main Authors: Lee, Jae-Seon, Oh, Su-Jin, Choi, Hyun-Jung, Kang, Joon Hee, Lee, Seon-Hyeong, Ha, Ji Sun, Woo, Sang Myung, Jang, Hyonchol, Lee, Ho, Kim, Soo-Youl
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 01.09.2020; MDPI
• Subjects: Adenocarcinoma; ATP production; ATPases; Calories; Cancer; Energy metabolism; fatty acid oxidation; Fatty acids; Glucose; Glycolysis; Health aspects; High fat diet; Hypocaloric diet; KC mouse; Lactic acid; Lipid peroxidation; Lipids; Low fat diet; Metabolic pathways; Metabolism; Metabolites; Mitochondria; Nutrient deficiency; Nutrients; Oxidation; Pancreas; Pancreatic cancer; PDAC; Physiological aspects; United States
• ISSN: 2072-6694; 2072-6694
• DOI: 10.3390/cancers12092477

Glycolysis is known as the main pathway for ATP production in cancer cells. However, in cancer cells, glucose deprivation for 24 h does not reduce ATP levels, whereas it does suppress lactate production. In this study, metabolic pathways were blocked to identify the main pathway of ATP production in pancreatic ductal adenocarcinoma (PDAC). Blocking fatty acid oxidation (FAO) decreased ATP production by 40% in cancer cells with no effect on normal cells. The effects of calorie balanced high- or low-fat diets were tested to determine whether cancer growth is modulated by fatty acids instead of calories. A low-fat diet caused a 70% decrease in pancreatic preneoplastic lesions compared with the control, whereas a high-fat diet caused a two-fold increase in preneoplastic lesions accompanied with increase of ATP production in the Kras (G12D)/Pdx1-cre PDAC model. The present results suggest that ATP production in cancer cells is dependent on FAO rather than on glycolysis, which can be a therapeutic approach by targeting cancer energy metabolism.