Kritsi Eftichia, Christodoulou Paris, Tsiaka Thalia, Georgiadis Panagiotis, Zervou Maria
Institute of Chemical Biology, National Hellenic Research Foundation, 48 Vassileos Constantinou Avenue, 11635 Athens, Greece.
Curr Issues Mol Biol. 2024 Apr 16;46(4):3394-3407. doi: 10.3390/cimb46040213.
Nowadays, the explosion of knowledge in the field of epigenetics has revealed new pathways toward the treatment of multifactorial diseases, rendering the key players of the epigenetic machinery the focus of today's pharmaceutical landscape. Among epigenetic enzymes, DNA methyltransferases (DNMTs) are first studied as inhibition targets for cancer treatment. The increasing clinical interest in DNMTs has led to advanced experimental and computational strategies in the search for novel DNMT inhibitors. Considering the importance of epigenetic targets as a novel and promising pharmaceutical trend, the present study attempted to discover novel inhibitors of natural origin against DNMTs using a combination of structure and ligand-based computational approaches. Particularly, a pharmacophore-based virtual screening was performed, followed by molecular docking and molecular dynamics simulations in order to establish an accurate and robust selection methodology. Our screening protocol prioritized five natural-derived compounds, derivatives of coumarins, flavones, chalcones, benzoic acids, and phenazine, bearing completely diverse chemical scaffolds from FDA-approved "Epi-drugs". Their total DNMT inhibitory activity was evaluated, revealing promising results for the derived hits with an inhibitory activity ranging within 30-45% at 100 µM of the tested compounds.
如今,表观遗传学领域知识的爆炸式增长揭示了治疗多因素疾病的新途径,使表观遗传机制的关键参与者成为当今药物领域的焦点。在表观遗传酶中,DNA甲基转移酶(DNMTs)最早被作为癌症治疗的抑制靶点进行研究。临床上对DNMTs的兴趣日益浓厚,促使人们在寻找新型DNMT抑制剂方面采用了先进的实验和计算策略。鉴于表观遗传靶点作为一种新颖且有前景的药物趋势的重要性,本研究尝试结合基于结构和配体的计算方法,发现天然来源的新型DNMT抑制剂。具体而言,进行了基于药效团的虚拟筛选,随后进行分子对接和分子动力学模拟,以建立一种准确且可靠的筛选方法。我们的筛选方案优先考虑了五种天然衍生化合物,即香豆素、黄酮、查耳酮、苯甲酸和吩嗪的衍生物,它们具有与FDA批准的“表观遗传药物”完全不同的化学支架。评估了它们对DNMT的总体抑制活性,结果显示,对于所筛选出的命中化合物,在100 μM测试化合物浓度下,其抑制活性在30%至45%之间,结果令人满意。