Lin Yiqi, Li Yuetong, Ke Caiying, Jin Ying, Lao Wanwen, Wu Yiling, Liu Yang, Kong Xinyi, Qiao Jie, Zhai Aixia, Bi Changlong
Department of Endocrinology, The Eighth Affiliated Hospital, Sun Yat-Sen University, Shenzhen, 518033, China.
Department of Laboratory Medicine, The Eighth Affiliated Hospital, Sun Yat-Sen University, Shenzhen, 518033, China.
Eur J Med Res. 2025 May 30;30(1):429. doi: 10.1186/s40001-025-02697-y.
Diabetes mellitus (DM) is a metabolic disease with complex pathogenic mechanisms. Histone deacetylase 4 (HDAC4) is a member of an important family of epigenetic modifications. An increasing amount of research indicates that HDAC4 may control DM by modulating the epigenetic and post-translational expression of numerous transcription factors and taking part in different signaling cascades. In this review, HDAC4 was reported to control the differentiation, growth, and function of pancreatic β-cells. Furthermore, HDAC4 regulates glucose metabolism by targeting GLUT4 and FOXO1 and further modulates insulin signaling pathways through cytoplasmic-nuclear shuttling. Moreover, HDAC4 has also been implicated in the regulation of diabetic nephropathy, diabetic cardiomyopathy, diabetes osteoporosis, diabetic wounds, and diabetic encephalopathy. Therefore, HDAC4 is consider to be a viable therapeutic target for the treatment of DM and its complications. HDAC inhibitors and other targeted inhibitions of HDAC4 provide us with new ideas for developing novel intervention strategies. This article reviews the role of HDAC4 in diabetes mellitus and its complications.
糖尿病(DM)是一种致病机制复杂的代谢性疾病。组蛋白去乙酰化酶4(HDAC4)是表观遗传修饰重要家族的一员。越来越多的研究表明,HDAC4可能通过调节众多转录因子的表观遗传和翻译后表达以及参与不同的信号级联反应来控制糖尿病。在本综述中,据报道HDAC4可控制胰腺β细胞的分化、生长和功能。此外,HDAC4通过靶向葡萄糖转运蛋白4(GLUT4)和叉头转录因子O1(FOXO1)来调节葡萄糖代谢,并通过胞质-核穿梭进一步调节胰岛素信号通路。此外,HDAC4还与糖尿病肾病、糖尿病心肌病、糖尿病骨质疏松症、糖尿病伤口和糖尿病脑病的调节有关。因此,HDAC4被认为是治疗糖尿病及其并发症的一个可行的治疗靶点。HDAC抑制剂和其他对HDAC4的靶向抑制为我们开发新的干预策略提供了新思路。本文综述了HDAC4在糖尿病及其并发症中的作用。