Zhang Yuan, Wang Zhihua, Ma Xiaoyao, Yang Shengnan, Hu Xueyan, Tao Jin, Hou Yuanyuan, Bai Gang
State Key Laboratory of Medicinal Chemical Biology, College of Pharmacy and Tianjin Key Laboratory of Molecular Drug Research, Nankai University, Tianjin 300353, China.
Acta Pharm Sin B. 2019 Mar;9(2):294-303. doi: 10.1016/j.apsb.2018.11.002. Epub 2018 Nov 27.
Members of the proto-oncogene superfamily are indispensable molecular switches that play critical roles in cell proliferation, differentiation, and cell survival. Recent studies have attempted to prevent the interaction of RAS/GTP with RAS guanine nucleotide exchange factors (GEFs), impair RAS-effector interactions, and suppress RAS localization to prevent oncogenic signalling. The present study aimed to investigate the effect of the natural triterpenoic acid inhibitor glycyrrhetinic acid, which is isolated from the roots of plant species, on RAS stability. We found that glycyrrhetinic acid may bind to the P-loop of RAS and alter its stability. Based on our biochemical tests and structural analysis results, glycyrrhetinic acid induced a conformational change in RAS. Meanwhile, glycyrrhetinic acid abolishes the function of RAS by interfering with the effector protein RAF kinase activation and RAS/MAPK signalling.
原癌基因超家族成员是不可或缺的分子开关,在细胞增殖、分化和细胞存活中发挥关键作用。最近的研究试图阻止RAS/GTP与RAS鸟嘌呤核苷酸交换因子(GEFs)的相互作用,破坏RAS效应器相互作用,并抑制RAS定位以防止致癌信号传导。本研究旨在探讨从植物物种根部分离出的天然三萜酸抑制剂甘草次酸对RAS稳定性的影响。我们发现甘草次酸可能与RAS的P环结合并改变其稳定性。基于我们的生化测试和结构分析结果,甘草次酸诱导了RAS的构象变化。同时,甘草次酸通过干扰效应蛋白RAF激酶激活和RAS/MAPK信号传导来消除RAS的功能。