Beak Myeonghun, Park Sungjin, Kim Jin-Hee, Eom Hyo Jin, Lee Ho-Yeon, Kim Yon Hui, Lee Jinhyuk, Nam Seungyoon
College of Medicine, Gachon University, Incheon 21565, Korea.
Gachon Institute of Genome Medicine and Science, Department of Genome Medicine and Science, Gachon University Gil Medical Center, Gachon University College of Medicine, Incheon 21565, Korea.
Cancers (Basel). 2022 Mar 22;14(7):1604. doi: 10.3390/cancers14071604.
Ras homologous A (RHOA), a signal mediator and a GTPase, is known to be associated with the progression of gastric cancer (GC), which is the fourth most common cause of death in the world. Previously, we designed pharmacologically optimized inhibitors against RHOA, including JK-136 and JK-139. Based on this previous work, we performed lead optimization and designed novel RHOA inhibitors for greater anti-GC potency. Two of these compounds, JK-206 and JK-312, could successfully inhibit the viability and migration of GC cell lines. Furthermore, using transcriptomic analysis of GC cells treated with JK-206, we revealed that the inhibition of RHOA might be associated with the inhibition of the mitogenic pathway. Therefore, JK-206 treatment for RHOA inhibition may be a new therapeutic strategy for regulating GC proliferation and migration.
Ras同源蛋白A(RHOA)是一种信号转导分子和GTP酶,已知其与胃癌(GC)的进展相关,胃癌是全球第四大常见死因。此前,我们设计了针对RHOA的药理学优化抑制剂,包括JK-136和JK-139。基于此前的工作,我们进行了先导化合物优化,并设计了新型RHOA抑制剂以提高抗胃癌效力。其中两种化合物JK-206和JK-312能够成功抑制胃癌细胞系的活力和迁移。此外,通过对用JK-206处理的胃癌细胞进行转录组分析,我们发现抑制RHOA可能与抑制促有丝分裂途径有关。因此,用JK-206抑制RHOA可能是调节胃癌增殖和迁移的一种新治疗策略。