Nicotinamide N‐methyltransferase decreases 5‐fluorouracil sensitivity in human esophageal squamous cell carcinoma through metabolic reprogramming and promoting the Warburg effect

• Published in: Molecular carcinogenesis Vol. 59; no. 8; pp. 940 - 954
• Main Authors: Cui, Yanyan, Yang, Dawei, Wang, Wenjie, Zhang, Luyu, Liu, Hongtao, Ma, Shanshan, Guo, Wenna, Yao, Minghao, Zhang, Kun, Li, Wencai, Zhang, Yanting, Guan, Fangxia
• Format: Journal Article
• Language: English
• Published: United States Wiley Subscription Services, Inc 01.08.2020
• Subjects: 5-Fluorouracil; Chemotherapy; Deoxyglucose; drug sensitivity; Esophageal cancer; esophageal squamous cell carcinoma; Esophagus; Gas chromatography; Glycolysis; Hexokinase; L-Lactate dehydrogenase; Lactic acid; Mass spectroscopy; Metabolism; metabonomics; Methyltransferase; Nicotinamide; nicotinamide N‐methyltransferase; Phosphoglycerate mutase; Squamous cell carcinoma; Tricarboxylic acid cycle; Tumor cells; Xenografts; 5-fluorouracil; esophageal squamous cell carcinoma; metabonomics; drug sensitivity; nicotinamide N-methyltransferase
• ISSN: 0899-1987; 1098-2744
• DOI: 10.1002/mc.23209

Esophageal squamous cell carcinoma (ESCC) is a common malignant tumor with poor prognosis. And different individuals respond to the same drug differently. Increasing evidence has confirmed that metabolism reprogramming was involved in the drug sensitivity of tumor cells. However, the potential molecular mechanism of 5‐fluorouracil (5‐FU) sensitivity remains to be elucidated in ESCC cells. In this study, we found that the 5‐FU sensitivity of TE1 cells was lower than that of EC1 and Eca109 cells. Gas chromatography‐mass spectrometry analysis results showed that nicotinate and nicotinamide metabolism and tricarboxylic acid cycle were significantly different in these three cell lines. Nicotinamide N‐methyltransferase (NNMT), a key enzyme of nicotinate and nicotinamide metabolism, was significantly higher expressed in TE1 cells than that in EC1 and Eca109 cells. Therefore, the function of NNMT on 5‐FU sensitivity was analyzed in vitro and in vivo. NNMT downregulation significantly increased 5‐FU sensitivity in TE1 cells. Meanwhile, the glucose consumption and lactate production were decreased, and the expression of glycolysis‐related enzymes hexokinase 2, lactate dehydrogenase A, and phosphoglycerate mutase 1 were downregulated in NNMT knockdown TE1 cells. Besides, overexpression of NNMT in EC1 and Eca109 cells caused the opposite effects. Moreover, when glycolysis was inhibited by 2‐deoxyglucose, the roles of NNMT on 5‐FU sensitivity was weakened. In vivo experiments showed that NNMT knockdown significantly increased the sensitivity of xenografts to 5‐FU and suppressed the Warburg effect. Overall, these results demonstrated that NNMT decreases 5‐FU sensitivity in human ESCC cells through promoting the Warburg effect, suggesting that NNMT may contribute to predict the treatment effects of the clinical chemotherapy in ESCC.