Cancer and Translational Research Laboratory, Dr. D. Y. Patil Biotechnology and Bioinformatics Institute, Dr. D. Y. Patil Vidyapeeth, Pune, Maharashtra, 411033, India.
Bioinformatics Research Laboratory, Dr. D. Y. Patil Biotechnology & Bioinformatics Institute, Dr. D.Y. Patil Vidyapeeth, Pune, 411033, Maharashtra, India.
Mol Divers. 2023 Dec;27(6):2867-2885. doi: 10.1007/s11030-022-10587-2. Epub 2022 Dec 21.
Peroxisome proliferator-activated receptors (PPAR)-α, a ligand-activated transcription factor stands out to be a valuable protein target against cancer. Given that ligand binding is the crucial process for the activation of PPAR-α, fibrate class of synthetic compounds serves as potent agonist for the receptor. However, their serious side effects limit the long-term application in cancer. This emphasizes the dire need to identify new candidates that would exert desired activation by abrogating the adverse effects caused by synthetic agonists. Natural dietary products serve as an important source of drug discovery. Hence, the present study encompasses the investigation of the role of natural plant phenolic compounds: kaempferol, resveratrol, and quercetin and their 8708 derivatives by the means of computational pipeline comprising molecular docking and molecular dynamic (MD) simulation techniques. Docking calculations shortlisted potential candidates, namely 6-cinnamylchrysin (6-CC), resveratrol potassium-4-sulfate (RPS) and 6-[2-(3,4-Dihydroxyphenyl)-5-hydroxy-4-oxochromen-7-yl]oxyhexyl nitrate (DHOON), and derivatives of kaempferol, resveratrol, and quercetin, respectively. 6-CC, RPS, and DHOON manifested better affinities of - 32.83 kcal/mol (Ala333, Lys358, His440), - 27.22 kcal/mol (Tyr314, Met355), and - 30.18 kcal/mol (Ser280, Tyr314, Ala333), respectively, and were found to act as good stimulants for PPAR-α. Among these three compounds, 6-CC caused relatively least deviations and fluctuations analyzed through MD simulation which judiciously held responsible to attain most favorable interaction with PPAR-α. Followed by the binding free energy (ΔG) calculations using MM-GBSA confirmed the key role of 6-CC toward PPAR-α. The compound 6-CC also achieved high drug-likeness and pharmacokinetic properties. Thus, these findings stipulate new drug leads for PPAR-α receptor which abets a way to develop new anti-cancer drugs.
过氧化物酶体增殖物激活受体 (PPAR)-α 是一种配体激活的转录因子,是一种有价值的抗癌蛋白靶标。鉴于配体结合是激活 PPAR-α 的关键过程,合成的纤维酸类化合物是该受体的有效激动剂。然而,它们的严重副作用限制了它们在癌症中的长期应用。这强调了迫切需要识别新的候选物,这些候选物通过消除合成激动剂引起的不良反应来发挥所需的激活作用。天然膳食产品是药物发现的重要来源。因此,本研究包括通过包含分子对接和分子动力学 (MD) 模拟技术的计算管道研究天然植物酚类化合物:山奈酚、白藜芦醇和槲皮素及其 8708 衍生物的作用。对接计算筛选出潜在的候选物,即 6-肉桂基白杨素 (6-CC)、白藜芦醇钾-4-硫酸盐 (RPS) 和 6-[2-(3,4-二羟基苯基)-5-羟基-4-氧代色满-7-基]氧基己基硝酸盐 (DHOON) 以及山奈酚、白藜芦醇和槲皮素的衍生物。6-CC、RPS 和 DHOON 表现出更好的亲和力,分别为-32.83 kcal/mol(Ala333、Lys358、His440)、-27.22 kcal/mol(Tyr314、Met355)和-30.18 kcal/mol(Ser280、Tyr314、Ala333),并且被发现是 PPAR-α 的良好刺激物。在这三种化合物中,6-CC 在 MD 模拟分析中引起的偏差和波动相对较小,这合理地负责与 PPAR-α 获得最有利的相互作用。随后使用 MM-GBSA 进行结合自由能 (ΔG) 计算,证实了 6-CC 对 PPAR-α 的关键作用。该化合物 6-CC 还具有较高的类药性和药代动力学特性。因此,这些发现为 PPAR-α 受体提供了新的药物先导,为开发新的抗癌药物开辟了途径。