Lung Jrhau, Chen Kuan-Liang, Hung Chien-Hui, Chen Chih-Cheng, Hung Ming-Szu, Lin Yu-Ching, Wu Ching-Yuan, Lee Kuan-Der, Shih Neng-Yao, Tsai Ying Huang
Department of Medical Research and Development, Chang Gung Memorial Hospital, Chiayi.
Department of Endodontics, ChiMei Medical Center, Tainan.
Drug Des Devel Ther. 2017 Nov 16;11:3281-3290. doi: 10.2147/DDDT.S149214. eCollection 2017.
Unlimited growth of cancer cells requires an extensive nutrient supply. To meet this demand, cancer cells drastically upregulate glucose uptake and metabolism compared to normal cells. This difference has made the blocking of glycolysis a fascinating strategy to treat this malignant disease. α-enolase is not only one of the most upregulated glycolytic enzymes in cancer cells, but also associates with many cellular processes or conditions important to cancer cell survival, such as cell migration, invasion, and hypoxia. Targeting α-enolase could simultaneously disturb cancer cells in multiple ways and, therefore, is a good target for anticancer drug development. In the current study, more than 22 million chemical structures meeting the criteria of Lipinski's rule of five from the ZINC database were docked to α-enolase by virtual screening. Twenty-four chemical structures with docking scores better than that of the enolase substrate, 2-phosphoglycerate, were further screened by the absorption, distribution, metabolism, excretion, and toxicity (ADMET) properties prediction. Four of them were classified as non-mutagenic, non-carcinogenic, and capable of oral administration where they showed steady interactions to α-enolase that were comparable, even superior, to the currently available inhibitors in molecular dynamics (MD) simulation. These compounds may be considered promising leads for further development of the α-enolase inhibitors and could help fight cancer metabolically.
癌细胞的无限增殖需要大量的营养供应。为满足这一需求,与正常细胞相比,癌细胞会大幅上调葡萄糖摄取和代谢。这种差异使得阻断糖酵解成为治疗这种恶性疾病的一种极具吸引力的策略。α-烯醇化酶不仅是癌细胞中上调最为显著的糖酵解酶之一,还与许多对癌细胞存活至关重要的细胞过程或条件相关,如细胞迁移、侵袭和缺氧。靶向α-烯醇化酶可以同时以多种方式干扰癌细胞,因此是抗癌药物开发的一个良好靶点。在本研究中,通过虚拟筛选将来自ZINC数据库的超过2200万个符合Lipinski五规则标准的化学结构与α-烯醇化酶进行对接。通过吸收、分布、代谢、排泄和毒性(ADMET)性质预测,进一步筛选出24个对接分数优于烯醇化酶底物2-磷酸甘油酸的化学结构。其中四个被归类为无致突变性、无致癌性且可口服,在分子动力学(MD)模拟中,它们与α-烯醇化酶表现出稳定的相互作用,甚至优于目前可用的抑制剂。这些化合物可被视为进一步开发α-烯醇化酶抑制剂的有前景的先导物,并有助于在代谢方面对抗癌症。