Department of Pharmacology, School of Pharmacy, Xinjiang Medical University, Urumqi, 830011, China.
Department of Pharmacology, School of Basic Medicine, Peking University, Beijing, 100191, China.
Curr Top Med Chem. 2024;24(3):192-200. doi: 10.2174/0115680266273421231222061620.
FTY720 is an analog of sphingosine-1-phosphate (S1P) derived from the ascomycete Cordyceps sinensis. As a new immunosuppressant, FTY720 is widely used to treat multiple sclerosis. FTY720 binds to the S1P receptor after phosphorylation, thereby exerting immunosuppressive effects. The nonphosphorylated form of FTY720 can induce cell apoptosis, enhance chemotherapy sensitivity, and inhibit tumor metastasis of multiple tumors by inhibiting SPHK1 (sphingosine kinase 1) and activating PP2A (protein phosphatase 2A) and various cell death pathways. FTY720 can induce neutrophil extracellular traps to neutralize and kill pathogens , thus exerting anti- infective effects. At present, a series of FTY720 derivatives, which have pharmacological effects such as anti-tumor and alleviating airway hyperresponsiveness, have been developed through structural modification. This article reviews the pharmacological effects of FTY720 and its derivatives.
FTY720 是来源于虫草属真菌的鞘氨醇-1-磷酸(S1P)类似物。作为一种新型免疫抑制剂,FTY720 被广泛用于治疗多发性硬化症。FTY720 在磷酸化后与 S1P 受体结合,从而发挥免疫抑制作用。非磷酸化形式的 FTY720 通过抑制 SPHK1(鞘氨醇激酶 1)和激活 PP2A(蛋白磷酸酶 2A)以及各种细胞死亡途径,可诱导细胞凋亡、增强化疗敏感性,并抑制多种肿瘤的转移。FTY720 可以诱导中性粒细胞胞外诱捕网来中和和杀死病原体,从而发挥抗感染作用。目前,通过结构修饰已经开发出一系列具有抗肿瘤和缓解气道高反应性等药理作用的 FTY720 衍生物。本文综述了 FTY720 及其衍生物的药理作用。