Department of Chemistry and Biochemistry, University of South Carolina, Columbia, SC 29208, USA.
Henry M. Jackson Foundation, Bethesda, MD, USA; Department of Pathology, Uniformed Services University, Bethesda, MD, USA.
Bioorg Med Chem. 2023 Feb 1;79:117171. doi: 10.1016/j.bmc.2023.117171. Epub 2023 Jan 13.
Small molecule NSC243928 binds with LY6K, a potential target for the treatment of triple-negative breast cancer, and induces cancer cell death with an unclear mechanism. We have developed chemical tools to identify the molecular mechanisms of NSC243928-LY6K interaction. Herein, we report on the development and synthesis of biotinylated and fluorophore-tethered derivatives of NSC243928 guided by docking studies and molecular dynamics. Surface plasmon resonance assay indicates that these derivatives retained a direct binding with LY6K protein. Confocal analysis revealed that nitrobenzoxadiazole (NBD) fluorophore tagged NSC243928 is retained in LY6K expressing cancer cells. These novel modified compounds will be employed in future in vitro and in vivo studies to understand the molecular mechanisms of NSC243928 mediated cancer cell death. These studies will pave the path for developing novel targeted therapeutics and understanding any potential side-effects of these treatments for hard-to-treat cancers such as triple-negative breast cancer or other cancers with high expression of LY6K.
小分子 NSC243928 与 LY6K 结合,LY6K 是治疗三阴性乳腺癌的潜在靶点,其诱导癌细胞死亡的机制尚不清楚。我们已经开发了化学工具来确定 NSC243928-LY6K 相互作用的分子机制。在此,我们报告了基于对接研究和分子动力学设计和合成的生物素化和荧光团连接的 NSC243928 衍生物。表面等离子体共振分析表明,这些衍生物与 LY6K 蛋白保持直接结合。共焦分析显示,硝基苯并恶二唑(NBD)荧光标记的 NSC243928 保留在表达 LY6K 的癌细胞中。这些新型修饰化合物将在未来的体外和体内研究中用于了解 NSC243928 介导的癌细胞死亡的分子机制。这些研究将为开发新型靶向治疗药物铺平道路,并了解这些治疗方法对三阴性乳腺癌或其他 LY6K 高表达癌症等难治性癌症的任何潜在副作用。