印尼药用植物活性化合物作为16型人乳头瘤病毒肿瘤蛋白E6和E7抑制剂候选物的分子对接研究

Riyanti Weni Syafitri, A. Fibriani, Reza Aditama
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引用次数: 1

摘要

由人乳头瘤病毒(HPV),特别是HPV 16(60.5%)感染引起的子宫颈癌病例每年持续增加,死亡率很高。目前的抗癌药物不仅针对癌细胞,而且针对健康细胞,可能会产生严重的副作用。因此,有必要寻找更安全的替代疗法,例如,使用天然产物中的活性化合物。本研究的目的是用硅片法寻找印尼药用植物中可能抑制宫颈癌主要致病蛋白E6和E7 HPV 16的活性化合物。本研究根据分子量、溶解度、胃肠道吸收指数和药物相似度等指标,从187种药用植物中筛选出711种活性化合物。通过分子对接法检测符合标准的化合物与E6和E7蛋白的亲和力和相互作用谱。结果显示,符合标准的化合物有164种。分子对接分析显示,9个最有效的化合物作为E6AP结合位点的E6抑制剂,6个化合物作为p53结合位点的E6抑制剂。此外,有11种最有效的化合物作为E7抑制剂。本研究结果表明,存在能够抑制E6和E7蛋白的天然化合物,具有进一步用作抗hpv药物的潜力。然而,需要进一步的研究来测试这些化合物的体外和体内。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Selection of Indonesian Medicinal Plant Active Compounds as Inhibitor Candidates of Oncoproteins E6 and E7 Human Papillomavirus Type 16 by Molecular Docking
Cervical cancer cases caused by infection with Human Papillomavirus (HPV), especially HPV 16 (60.5% of cases) continue to increase every year with a high mortality rate. The current anti-cancer drugs were not only specifically targeting cancer cells, but healthy cells and can cause serious side effects. Therefore, it is necessary to find safer alternative therapies, e.g., using active compounds from natural products. The purpose of this study was to find the active compounds of Indonesian medicinal plants potentially as an inhibitor of oncoprotein E6 and E7 HPV 16, the main protein causing cervical cancer by in silico method. In this study, 711 active compounds from 187 medicinal plant species were selected based on molecular weight, solubility, gastrointestinal absorption index, and drug-likeness. Compounds that meet the criteria were tested for their affinity and interaction profile with E6 and E7 proteins through the molecular docking method. The results of this study showed 164 compounds that met the criteria. The molecular docking analysis showed nine of the most potent compounds as E6 inhibitors on the E6AP binding site and six compounds on the p53 binding site. Besides that, there were eleven most potent compounds as E7 inhibitors.  The results of this study indicate that there are natural compounds that can inhibit E6 and E7 proteins and have further potential to be used as anti-HPV drugs. However, further research is needed to test these compounds in vitro and in vivo.
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