首页> 外文期刊>Journal of Medicinal Chemistry >Discovery of 5,6-Bis(4-methoxy-3-methylphenyl)pyridin-2-amine as a WSB1 Degrader to Inhibit Cancer Cell Metastasis
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Discovery of 5,6-Bis(4-methoxy-3-methylphenyl)pyridin-2-amine as a WSB1 Degrader to Inhibit Cancer Cell Metastasis

机译:发现5,6-双(4-甲氧基-3-甲基苯基)吡啶-2-胺作为WSB1降解剂抑制癌细胞转移

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摘要

The gain of cell motility is an essential prerequisite for cancer metastasis. The ubiquitin ligase subunit WD repeat and SOCS box-containing 1 (WSB1) has been demonstrated to regulate hypoxia-driven tumor cell migration. However, there is still a lack of methods for discovering inhibitors targeting the WSB1 axis. Here, we employed phenotypic screening models and identified compound 4 that displayed migration inhibitory activity against WSB1-overexpressing cells. Further studies indicated that it may function as a WSB1 degrader, thus leading to the accumulation of the Rho guanosine diphosphate dissociation inhibitor 2 (RhoGDI2) protein, reversing the expression of downstream F-actin and formation of membrane ruffles, and disturbing the migration capacity of cancer cells. Moreover, compound 4 exhibited a promising in vivo anticancer metastatic effects. Our findings show the discovery of a new WSB1 degrader, providing a unique solution for the treatment of cancer metastasis.
机译:细胞运动的获得是癌症转移的必要前提。泛素连接酶亚基 WD 重复序列和含 SOCS 盒 1 (WSB1) 已被证明可调节缺氧驱动的肿瘤细胞迁移。然而,仍然缺乏发现靶向WSB1轴的抑制剂的方法。在这里,我们采用了表型筛选模型,并鉴定了对WSB1过表达细胞具有迁移抑制活性的化合物4。进一步的研究表明,它可能作为WSB1降解剂发挥作用,从而导致Rho鸟苷二磷酸解离抑制剂2(RhoGDI2)蛋白的积累,逆转下游F-肌动蛋白的表达和膜褶皱的形成,并扰乱癌细胞的迁移能力。此外,化合物4表现出有希望的体内抗癌转移作用。我们的研究结果表明发现了一种新的WSB1降解剂,为癌症转移的治疗提供了独特的解决方案。

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