针对人类notch 3蛋白的癌症的多方面靶向策略:一项计算研究。

In Silico Pharmacology Pub Date : 2021-09-29 eCollection Date: 2021-01-01 DOI:10.1007/s40203-021-00112-y
S Saranyadevi
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引用次数: 0

摘要

Notch受体在多种多细胞生物的发育和细胞命运调控中发挥着重要作用。对于正常分化,基因组是必不可少的,因为它们在癌症中的正常作用和作用是失调的。Notch 3已被证明在肺癌功能中发挥重要作用,因此,抑制Notch 3蛋白激活代表了癌症治疗的明确计划。本研究完成了基于结构和配体的药效团联合假说,以探索新的notch 3抑制剂。分析发现,常见的铅分子ZINC000013449462的XP GScore和结合能评分均高于参考抑制剂DAPT。所鉴定的先导化合物通过了所有可用药特征,结合稳定。此外,导联分子还可以与notch 3蛋白活性袋的结合位点残基Asp1621和Arg1465分别形成氢桥和盐桥相互作用。本质上,采用深度神经网络算法在109个NSCLC细胞系中验证了hit的抑制活性。我们的研究表明,ZINC000013449462可能是notch 3靶点的原型分子,并将在临床研究中进一步检验其对抗NSCLC的能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Multifaceted targeting strategies in cancer against the human notch 3 protein: a computational study.

Multifaceted targeting strategies in cancer against the human notch 3 protein: a computational study.

Notch receptors play a significant role in the development and the regulation of cell-fate in several multicellular organisms. For normal differentiation, genomes are essential as their regular roles and play a role in cancer is dysregulated. Notch 3 has been shown to play a major role in lung cancer function and therefore, inhibition of notch 3 protein activation represents a clear plan for cancer treatment. This study accomplished a combined structure- and ligand-based pharmacophore hypothesis to explore novel notch 3 inhibitors. The analysis identified common lead molecule ZINC000013449462 that showed better XP GScore and binding energy score than the reference inhibitor DAPT. The identified lead compound that passed all the druggable characteristics exhibited stable binding. Furthermore, the lead molecule can also form hydrogen and salt bridge interactions with binding site residues Asp1621 and Arg1465 residues, respectively of the active pockets of notch 3 protein. In essence, the inhibitory activity of the hit was validated across 109 NSCLC cell lines by employing a deep neural network algorithm. Our study proposes that ZINC000013449462 would be a possible prototype molecule towards the notch 3 target and further examined by clinical studies to combat NSCLC.

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