Wang Y, Xu J, Xia C
Department of Pathogenic Biology, School of Biology & Basic Medical Sciences, Suzhou Medical College of Soochow University, Suzhou, Jiangsu 215123, China.
Zhongguo Xue Xi Chong Bing Fang Zhi Za Zhi. 2024 Mar 25;36(2):207-214. doi: 10.16250/j.32.1374.2023178.
Schistosomiasis is a neglected zoonotic parasitic disease. Currently, praziquantel is the drug of choice for the treatment of schistosomiasis, and is the only effective chemical for treatment of schistosomiasis japonica. Since its introduction in the 1970s, praziquantel has been used for large-scale chemotherapy of schistosomiasis for over 40 years. However, there have been reports pertaining to the resistance to praziquantel in schistosomes. Therefore, development of novel antischistosomal agents as alternatives of praziquantel, is of great need. Histone deacetylases and histone acetyltransferases have been recently reported to play critical roles in the growth, development and reproduction of schistosomes, and are considered as potential drug targets for the treatment of schistosomiasis. This review summarizes the latest advances of histone deacetylase and histone acetyltransferase inhibitors in the research on antischistosomal drugs, so as to provide insights into research and development of novelantischistosomal agents.
血吸虫病是一种被忽视的人畜共患寄生虫病。目前,吡喹酮是治疗血吸虫病的首选药物,也是治疗日本血吸虫病的唯一有效化学药物。自20世纪70年代引入以来,吡喹酮已用于血吸虫病的大规模化疗40多年。然而,已有关于血吸虫对吡喹酮耐药的报道。因此,迫切需要开发新型抗血吸虫药物作为吡喹酮的替代品。最近有报道称,组蛋白去乙酰化酶和组蛋白乙酰转移酶在血吸虫的生长、发育和繁殖中起关键作用,并被视为治疗血吸虫病的潜在药物靶点。本文综述了组蛋白去乙酰化酶和组蛋白乙酰转移酶抑制剂在抗血吸虫药物研究中的最新进展,以期为新型抗血吸虫药物的研发提供思路。