Institute of Obstetrics and Gynecology, Università Cattolica del Sacro Cuore, Rome, Italy.
Department of Woman and Child Health, Fondazione Policlinico Universitario A. Gemelli, IRCCS, Rome, Italy.
Sci Rep. 2018 Oct 30;8(1):16047. doi: 10.1038/s41598-018-34471-y.
The NIMA (never in mitosis, gene A)-related kinase-6 (NEK6), which is implicated in cell cycle control and plays significant roles in tumorigenesis, is an attractive target for the development of novel anti-cancer drugs. Here we describe the discovery of a potent ATP site-directed inhibitor of NEK6 identified by virtual screening, adopting both structure- and ligand-based techniques. Using a homology-built model of NEK6 as well as the pharmacophoric features of known NEK6 inhibitors we identified novel binding scaffolds. Twenty-five compounds from the top ranking hits were subjected to in vitro kinase assays. The best compound, i.e. compound 8 ((5Z)-2-hydroxy-4-methyl-6-oxo-5-[(5-phenylfuran-2-yl)methylidene]-5,6-dihydropyridine-3-carbonitrile), was able to inhibit NEK6 with low micromolar IC value, also displaying antiproliferative activity against a panel of human cancer cell lines. Our results suggest that the identified inhibitor can be used as lead candidate for the development of novel anti-cancer agents, thus opening the possibility of new therapeutic strategies.
NIMA(有丝分裂期从未出现,基因 A)相关激酶-6(NEK6)与细胞周期调控有关,在肿瘤发生中起重要作用,是开发新型抗癌药物的有吸引力的靶标。在这里,我们描述了通过虚拟筛选发现的一种有效的 ATP 位向 NEK6 抑制剂,采用了结构和配体基两种技术。我们使用 NEK6 的同源构建模型以及已知 NEK6 抑制剂的药效特征来确定新的结合支架。从排名最高的 25 个化合物中选择了 25 个化合物进行体外激酶测定。最好的化合物,即化合物 8((5Z)-2-羟基-4-甲基-6-氧代-5-[(5-苯基呋喃-2-基)亚甲基]-5,6-二氢吡啶-3-甲腈),能够以低微摩尔 IC 值抑制 NEK6,同时对一系列人类癌细胞系显示出抗增殖活性。我们的结果表明,所鉴定的抑制剂可用作开发新型抗癌药物的先导候选物,从而为新的治疗策略开辟了可能性。