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硝呋太尔再利用于新型凋亡依赖性抗癌和抗菌药物的设计和合成:生物学评价、动力学研究和分子模拟。

Nitrofurazone repurposing towards design and synthesis of novel apoptotic-dependent anticancer and antimicrobial agents: Biological evaluation, kinetic studies and molecular modeling.

机构信息

Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Alexandria University, Alexandria 21521, Egypt.

Department of Medical Microbiology and Immunology, Faculty of Medicine, Alexandria University, Alexandria 21521, Egypt.

出版信息

Bioorg Chem. 2021 Aug;113:104971. doi: 10.1016/j.bioorg.2021.104971. Epub 2021 May 7.

Abstract

Drug repurposing has gained much attention as a cost-effective strategy that plays an exquisite role in identifying undescribed biological activities in clinical drugs. In the present work, we report the repurposing of the antibacterial drug nitrofurazone (NFZ) as a potential anticancer agent against CaCo-2, MDA-MB 231 and HepG-2 cancer cell lines. Novel series of nitrofurazone analogs were then designed considering the important pharmacologic features present in NFZ. Synthesis and biological evaluation of the target compounds revealed their promising anticancer activities endowed with antimicrobial potential and possessing better lipophilicity than NFZ. Compound 7, exclusively, inhibited the growth of all tested cancer cells more potently than NFZ with the least cytotoxicity against normal cells, displaying anti Gram-positive bacterial activities and antifungal potential. Analysis of the stereo-electronic properties of compound 7 via investigating the energies of HOMO, LUMO, HOMO-LUMO energy gap and MEP maps demonstrated its high reactivity and the expected molecular mechanism of action through reduction of the 5-nitrofuryl moiety. Data of the bioactivity studies indicated that the potent anticancer activity of 7 is mainly through increasing intracellular ROS levels and induction of apoptosis via significantly down-regulating the expression of Bcl-2 while up-regulating BAX, p53 and caspase 3 expression levels. Compound 7 potently inhibited the cellular expression levels of antioxidant enzymes GPx1 and GR compared to NFZ. Antioxidant enzymes kinetic studies and blind molecular docking simulations disclosed the mechanistic and structural aspects of the interaction between 7 and both GR and GPx1. Thus, the successful discovery of 7 as a potential dual anticancer-antimicrobial nitrofurazone analog might validate the applicability of drug repurposing strategy in unravelling the unrecognized bioactivity of the present conventional drugs, besides furnishing the way towards more optimization and development studies.

摘要

药物重定位作为一种具有成本效益的策略,在鉴定临床药物中未描述的生物活性方面发挥了重要作用,引起了广泛关注。在本工作中,我们报告了将抗菌药物硝呋太尔(NFZ)重新用于鉴定 CaCo-2、MDA-MB 231 和 HepG-2 癌细胞系的潜在抗癌药物。然后考虑到 NFZ 中存在的重要药理特征,设计了一系列新的硝呋太尔类似物。目标化合物的合成和生物评价揭示了它们具有潜在的抗癌活性,具有抗菌潜力,并且比 NFZ 具有更好的亲脂性。化合物 7 单独对所有测试的癌细胞的生长抑制作用比 NFZ 更强,对正常细胞的细胞毒性最小,显示出抗革兰氏阳性细菌活性和抗真菌潜力。通过研究 HOMO、LUMO、HOMO-LUMO 能隙和 MEP 图谱中化合物 7 的立体电子性质的分析,证明了其高反应性和预期的作用机制,即通过还原 5-硝基呋喃部分。生物活性研究数据表明,7 的强抗癌活性主要是通过增加细胞内 ROS 水平和通过显著下调 Bcl-2 的表达并上调 BAX、p53 和 caspase 3 的表达水平诱导细胞凋亡。与 NFZ 相比,7 能强烈抑制细胞抗氧化酶 GPx1 和 GR 的表达水平。抗氧化酶动力学研究和盲目分子对接模拟揭示了 7 与 GR 和 GPx1 之间相互作用的机制和结构方面。因此,成功发现 7 作为一种潜在的双重抗癌-抗菌硝呋太尔类似物,可能验证了药物重定位策略在揭示现有常规药物未被认识的生物活性方面的适用性,同时为进一步优化和开发研究提供了途径。

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