Niture Suryakant, Lin Minghui, Rios-Colon Leslimar, Qi Qi, Moore John T, Kumar Deepak
Julius L. Chambers Biomedical Biotechnology Research Institute, North Carolina Central University Durham, NC 27707, USA.
The Fourth People's Hospital of Ningxia Hui Autonomous Region, Yinchuan, China 750021.
Int J Hepatol. 2021 Apr 22;2021:6675762. doi: 10.1155/2021/6675762. eCollection 2021.
Autophagy is a conserved catabolic process that eliminates dysfunctional cytosolic biomolecules through vacuole-mediated sequestration and lysosomal degradation. Although the molecular mechanisms that regulate autophagy are not fully understood, recent work indicates that dysfunctional/impaired autophagic functions are associated with the development and progression of nonalcoholic fatty liver disease (NAFLD), alcoholic fatty liver disease (AFLD), and hepatocellular carcinoma (HCC). Autophagy prevents NAFLD and AFLD progression through enhanced lipid catabolism and decreasing hepatic steatosis, which is characterized by the accumulation of triglycerides and increased inflammation. However, as both diseases progress, autophagy can become impaired leading to exacerbation of both pathological conditions and progression into HCC. Due to the significance of impaired autophagy in these diseases, there is increased interest in studying pathways and targets involved in maintaining efficient autophagic functions as potential therapeutic targets. In this review, we summarize how impaired autophagy affects liver function and contributes to NAFLD, AFLD, and HCC progression. We will also explore how recent discoveries could provide novel therapeutic opportunities to effectively treat these diseases.
自噬是一种保守的分解代谢过程,通过液泡介导的隔离和溶酶体降解来清除功能失调的胞质生物分子。尽管调节自噬的分子机制尚未完全阐明,但最近的研究表明,自噬功能失调/受损与非酒精性脂肪性肝病(NAFLD)、酒精性脂肪性肝病(AFLD)和肝细胞癌(HCC)的发生和发展有关。自噬通过增强脂质分解代谢和减少肝脂肪变性来防止NAFLD和AFLD的进展,肝脂肪变性的特征是甘油三酯积累和炎症增加。然而,随着这两种疾病的进展,自噬可能会受损,导致两种病理状况加剧并进展为HCC。由于自噬受损在这些疾病中的重要性,人们对研究维持有效自噬功能的途径和靶点作为潜在治疗靶点的兴趣日益增加。在这篇综述中,我们总结了自噬受损如何影响肝功能并促进NAFLD、AFLD和HCC的进展。我们还将探讨最近的发现如何为有效治疗这些疾病提供新的治疗机会。