新陈代谢
脂肪变性
生物化学
脂肪性肝炎
氨基酸
生物
β氧化
脂肪酸代谢
氨基酸代谢
代谢途径
碳水化合物代谢
脂质代谢
线粒体
肝细胞癌
非酒精性脂肪肝
功能(生物学)
疾病
化学
脂肪肝
胆汁酸
单糖
生物信息学
过氧化物酶体
能量代谢
非酒精性脂肪性肝炎
肝病
细胞呼吸
医学
氧化代谢
作者
Min Wu,J. Liu,Xiaoqi Sun,Lu Zhang,Lin Yu
标识
DOI:10.53941/sen.2026.100001
摘要
Metabolic dysfunction-associated steatotic liver disease (MASLD) has been proposed as a more precise term to characterize steatosis amid metabolic dysregulation and is projected to emerge as the predominant cause of hepatocellular carcinoma (HCC) globally, given the rising prevalence of metabolic comorbidities. Particularly in its inflammatory form, known as metabolic dysfunction-associated steatohepatitis (MASH), hepatic metabolism is profoundly altered. Amino acids are fundamental building blocks that support cellular metabolism and biosynthesis, alongside monosaccharides and fatty acids. Emerging research suggests that aberrant amino acid metabolism in MASLD/MASH and HCC impacts mitochondrial function and redox equilibrium. Nonetheless, the involvement of amino acid metabolism in the progression from MASLD/MASH to HCC is still inadequately comprehended. This review summarizes the aberrant amino acid metabolism in MASLD/MASH and HCC, as well as nanomedicine-based approaches for modulating this metabolism to facilitate the discovery of more effective biomarkers and precision therapeutics for the prevention of MASLD/MASH and HCC.
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