Zheng Tianpeng, Wang Shanglong, Liu Wukun, Lu Yunlong
Jiangsu Collaborative Innovation Center of Chinese Medicinal Resources Industrialization, School of Medicine, Nanjing University of Chinese Medicine, Nanjing 210023, China.
J Med Chem. 2025 Jan 23;68(2):1002-1020. doi: 10.1021/acs.jmedchem.4c02613. Epub 2025 Jan 6.
The lysine acetyltransferase 6A (KAT6A, MOZ, MYST3) is a member of the MYST family of protein acetyltransferases, which are essential for different biological processes such as craniofacial, embryonic, stem cell development, and hematopoiesis. KAT6A is an oncogene in human acute myeloid leukemia (AML), and KAT6A overexpression in AML is associated with metastases and poor prognoses. Furthermore, KAT6A mutations play an important role in cancer formation and progression and result in therapeutic resistance in both hematopoietic malignancies and solid tumors. In this review, we discuss the structural and biological functions of KAT6A and summarize the influence of KAT6A in the development of various tumors. In addition, the recent KAT6A/B inhibitors, their anticancer activities, challenges, and perspective of developing KAT6A/B inhibitors as anticancer drug candidates were introduced.
赖氨酸乙酰转移酶6A(KAT6A,MOZ,MYST3)是蛋白质乙酰转移酶MYST家族的成员,该家族对于不同的生物学过程至关重要,如颅面、胚胎、干细胞发育和造血作用。KAT6A是人类急性髓系白血病(AML)中的一种癌基因,AML中KAT6A的过表达与转移和不良预后相关。此外,KAT6A突变在癌症形成和进展中起重要作用,并导致造血系统恶性肿瘤和实体瘤的治疗耐药性。在本综述中,我们讨论了KAT6A的结构和生物学功能,并总结了KAT6A在各种肿瘤发生发展中的影响。此外,还介绍了最近的KAT6A/B抑制剂、它们的抗癌活性、挑战以及将KAT6A/B抑制剂开发为抗癌候选药物的前景。