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
Division of Cancer Biology, Research Institute, National Cancer Center, Goyang 10408, Korea.
Center for Liver and Pancreatobiliary Cancer, National Cancer Center, Goyang 10408, Korea.
Cancers (Basel). 2020 Sep 1;12(9):2477. 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.
糖酵解被认为是癌细胞中产生ATP的主要途径。然而,在癌细胞中,24小时的葡萄糖剥夺并不会降低ATP水平,而它确实会抑制乳酸的产生。在本研究中,通过阻断代谢途径来确定胰腺导管腺癌(PDAC)中ATP产生的主要途径。阻断脂肪酸氧化(FAO)使癌细胞中的ATP产生减少40%,而对正常细胞没有影响。测试了热量平衡的高脂肪或低脂肪饮食的效果,以确定癌症生长是否由脂肪酸而非热量调节。与对照组相比,低脂肪饮食使胰腺肿瘤前病变减少了70%,而高脂肪饮食使肿瘤前病变增加了两倍,同时在Kras(G12D)/Pdx1-cre PDAC模型中ATP产生增加。目前的结果表明,癌细胞中的ATP产生依赖于FAO而非糖酵解,这可能是一种通过靶向癌症能量代谢的治疗方法。