Graduate School of System Informatics, Kobe University, 1-1 Rokkodai, Nada-ku, Kobe 657-8501, Japan.
Int J Mol Sci. 2024 May 14;25(10):5347. doi: 10.3390/ijms25105347.
The PAX8/PPARγ rearrangement, producing the PAX8-PPARγ fusion protein (PPFP), is thought to play an essential role in the oncogenesis of thyroid follicular tumors. To identify PPFP-targeted drug candidates and establish an early standard of care for thyroid tumors, we performed ensemble-docking-based compound screening. Specifically, we investigated the pocket structure that should be adopted to search for a promising ligand compound for the PPFP; the position of the ligand-binding pocket on the PPARγ side of the PPFP is similar to that of PPARγ; however, the shape is slightly different between them due to environmental factors. We developed a method for selecting a PPFP structure with a relevant pocket and high prediction accuracy for ligand binding. This method was validated using PPARγ, whose structure and activity values are known for many compounds. Then, we performed docking calculations to the PPFP for 97 drug or drug-like compounds registered in the DrugBank database with a thiazolidine backbone, which is one of the characteristics of ligands that bind well to PPARγ. Furthermore, the binding affinities of promising ligand candidates were estimated more reliably using the molecular mechanics Poisson-Boltzmann surface area method. Thus, we propose promising drug candidates for the PPFP with a thiazolidine backbone.
PAX8/PPARγ 重排产生 PAX8-PPARγ 融合蛋白(PPFP),被认为在甲状腺滤泡肿瘤的发生中起关键作用。为了鉴定 PPFP 靶向药物候选物并为甲状腺肿瘤建立早期治疗标准,我们进行了基于集合对接的化合物筛选。具体来说,我们研究了应该采用的口袋结构,以寻找针对 PPFP 的有前途的配体化合物;PPFP 上 PPARγ 侧的配体结合口袋的位置与 PPARγ 相似;然而,由于环境因素,它们的形状略有不同。我们开发了一种选择具有相关口袋和高配体结合预测准确性的 PPFP 结构的方法。该方法使用 PPARγ 进行了验证,已知许多化合物的结构和活性值。然后,我们对 DrugBank 数据库中注册的 97 种具有噻唑烷骨架的药物或类药物化合物进行了对接计算,噻唑烷骨架是与 PPARγ 结合良好的配体的特征之一。此外,使用分子力学泊松-玻尔兹曼表面积方法更可靠地估计了有前途的配体候选物的结合亲和力。因此,我们提出了具有噻唑烷骨架的针对 PPFP 的有前途的药物候选物。