Department of Laboratory Medicine, National Institutes of Health, Bethesda, MD, 20892, USA.
Department of Physiology and Pharmacology, University of Western Ontario, London, ON, Canada.
Sci Rep. 2022 Oct 17;12(1):17372. doi: 10.1038/s41598-022-21342-w.
The small GTPase Cdc42 is an integral component of the cytoskeleton, and its dysregulation leads to pathophysiological conditions, such as cancer. Binding of Cdc42 to the scaffold protein IQGAP1 stabilizes Cdc42 in its active form. The interaction between Cdc42 and IQGAP1 enhances migration and invasion of cancer cells. Disrupting this association could impair neoplastic progression and metastasis; however, no effective means to achieve this has been described. Here, we screened 78,500 compounds using a homogeneous time resolved fluorescence-based assay to identify small molecules that disrupt the binding of Cdc42 to IQGAP1. From the combined results of the validation assay and counter-screens, we selected 44 potent compounds for cell-based experiments. Immunoprecipitation and cell viability analysis rendered four lead compounds, namely NCGC00131308, NCGC00098561, MLS000332963 and NCGC00138812, three of which inhibited proliferation and migration of breast carcinoma cells. Microscale thermophoresis revealed that two compounds bind directly to Cdc42. One compound reduced the amount of active Cdc42 in cells and effectively impaired filopodia formation. Docking analysis provided plausible models of the compounds binding to the hydrophobic pocket adjacent to the GTP binding site of Cdc42. In conclusion, we identified small molecules that inhibit binding between Cdc42 and IQGAP1, which could potentially yield chemotherapeutic agents.
小分子 GTPase Cdc42 是细胞骨架的重要组成部分,其功能失调会导致生理病理状态,如癌症。Cdc42 与支架蛋白 IQGAP1 的结合稳定了 Cdc42 的活性形式。Cdc42 与 IQGAP1 的相互作用增强了癌细胞的迁移和侵袭。破坏这种关联可能会损害肿瘤的进展和转移;然而,尚未描述有效的方法来实现这一目标。在这里,我们使用均相时间分辨荧光测定法筛选了 78500 种化合物,以鉴定破坏 Cdc42 与 IQGAP1 结合的小分子。根据验证试验和对照筛选的综合结果,我们选择了 44 种有效的化合物进行细胞实验。免疫沉淀和细胞活力分析得到了四种先导化合物,即 NCGC00131308、NCGC00098561、MLS000332963 和 NCGC00138812,其中三种化合物抑制了乳腺癌细胞的增殖和迁移。微量热泳法显示两种化合物直接与 Cdc42 结合。一种化合物减少了细胞中活性 Cdc42 的量,并有效地抑制了丝状伪足的形成。对接分析提供了化合物与 Cdc42 的 GTP 结合位点相邻的疏水性口袋结合的合理模型。总之,我们鉴定了抑制 Cdc42 与 IQGAP1 结合的小分子,它们可能成为化学治疗剂。