调节器
癌症研究
激酶
激活剂(遗传学)
有丝分裂
癌细胞
癌症
医学
药理学
生物
细胞生物学
受体
内科学
遗传学
基因
作者
Ana Monfort‐Vengut,Guillermo de Cárcer
出处
期刊:Pharmaceutics
[Multidisciplinary Digital Publishing Institute]
日期:2023-04-13
卷期号:15 (4): 1232-1232
被引量:12
标识
DOI:10.3390/pharmaceutics15041232
摘要
Rigosertib (ON-01910.Na) is a small-molecule member of the novel synthetic benzyl-styryl-sulfonate family. It is currently in phase III clinical trials for several myelodysplastic syndromes and leukemias and is therefore close to clinical translation. The clinical progress of rigosertib has been hampered by a lack of understanding of its mechanism of action, as it is currently considered a multi-target inhibitor. Rigosertib was first described as an inhibitor of the mitotic master regulator Polo-like kinase 1 (Plk1). However, in recent years, some studies have shown that rigosertib may also interact with the PI3K/Akt pathway, act as a Ras–Raf binding mimetic (altering the Ras signaling pathway), as a microtubule destabilizing agent, or as an activator of a stress-induced phospho-regulatory circuit that ultimately hyperphosphorylates and inactivates Ras signaling effectors. Understanding the mechanism of action of rigosertib has potential clinical implications worth exploring, as it may help to tailor cancer therapies and improve patient outcomes.
科研通智能强力驱动
Strongly Powered by AbleSci AI