Cai Qiuyu, Gan Can, Tang Chengwei, Wu Hao, Gao Jinhang
Laboratory of Gastroenterology and Hepatology, West China Hospital, Sichuan University, Chengdu, China.
Department of Gastroenterology, West China Hospital, Sichuan University, Chengdu, China.
Front Pharmacol. 2021 Nov 23;12:784591. doi: 10.3389/fphar.2021.784591. eCollection 2021.
Chronic liver disease (CLD) represents a global health problem, accounting for the heavy burden of disability and increased health care utilization. Epigenome alterations play an important role in the occurrence and progression of CLD. Histone modifications, which include acetylation, methylation, and phosphorylation, represent an essential part of epigenetic modifications that affect the transcriptional activity of genes. Different from genetic mutations, histone modifications are plastic and reversible. They can be modulated pharmacologically without changing the DNA sequence. Thus, there might be chances to establish interventional solutions by targeting histone modifications to reverse CLD. Here we summarized the roles of histone modifications in the context of alcoholic liver disease (ALD), metabolic associated fatty liver disease (MAFLD), viral hepatitis, autoimmune liver disease, drug-induced liver injury (DILI), and liver fibrosis or cirrhosis. The potential targets of histone modifications for translation into therapeutics were also investigated. In prospect, high efficacy and low toxicity drugs that are selectively targeting histone modifications are required to completely reverse CLD and prevent the development of liver cirrhosis and malignancy.
慢性肝病(CLD)是一个全球性的健康问题,造成了沉重的残疾负担并增加了医疗保健的使用。表观基因组改变在CLD的发生和发展中起重要作用。组蛋白修饰,包括乙酰化、甲基化和磷酸化,是影响基因转录活性的表观遗传修饰的重要组成部分。与基因突变不同,组蛋白修饰具有可塑性和可逆性。它们可以通过药理学方法进行调节而不改变DNA序列。因此,有可能通过靶向组蛋白修饰来建立干预方案以逆转CLD。在此,我们总结了组蛋白修饰在酒精性肝病(ALD)、代谢相关脂肪性肝病(MAFLD)、病毒性肝炎、自身免疫性肝病、药物性肝损伤(DILI)以及肝纤维化或肝硬化中的作用。还研究了可转化为治疗方法的组蛋白修饰潜在靶点。展望未来,需要有选择性地靶向组蛋白修饰的高效低毒药物来完全逆转CLD并预防肝硬化和恶性肿瘤的发生。