{"title":"Synergistic action of JNK activation and BChE inhibition: a novel anti- glioblastoma compound with neuroprotective profile.","authors":"Ziyao Lu, Qinghong Liao, Yuetong Duan, Kaixuan Wang, Siyu He, Weiping Lyu, Xuehong Chen, Qi Li","doi":"10.1080/17568919.2026.2658833","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>This study aims to investigate whether butyrylcholinesterase (BChE) inhibitor <b>QY-54</b> can be used to treat glioblastoma (GBM) and exert a neuroprotective profile.</p><p><strong>Methods: </strong>At the cellular level, the effects of <b>QY-54</b> on the proliferation, invasion, and migration of GBM cells from different species were investigated. At the animal level, the safety of <b>QY-54</b> in normal mice, its anti-tumor effects in GBM mice, and its effects on cognition protective function were examined.</p><p><strong>Results: </strong>At the cellular level, <b>QY-54</b> exhibited significant inhibitory effects on the proliferation, migration, and invasion of GBM cells derived from different species. At the animal level, <b>QY-54</b> showed low toxicity in normal mice. Moreover, it significantly inhibited GBM tumor growth, promoted tumor cell apoptosis, suppressed neuroinflammation, protected neurons, and improved the general condition and cognitive function of GBM mice. In Western blot experiments, <b>QY-54</b> upregulated c-jun N-terminal kinase (JNK) levels to exert an inhibitory effect on glioma.</p><p><strong>Conclusion: </strong><b>QY-54</b> exhibits dual effects of anti-glioblastoma and cognitive improvement, by inhibiting BChE and activating the JNK signaling pathway. <b>QY-54</b> is a highly promising drug for the treatment of glioblastoma with neuroprotective profile.</p>","PeriodicalId":12475,"journal":{"name":"Future medicinal chemistry","volume":" ","pages":"1377-1389"},"PeriodicalIF":3.3000,"publicationDate":"2026-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13228976/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Future medicinal chemistry","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/17568919.2026.2658833","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/4/15 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0
Abstract
Objective: This study aims to investigate whether butyrylcholinesterase (BChE) inhibitor QY-54 can be used to treat glioblastoma (GBM) and exert a neuroprotective profile.
Methods: At the cellular level, the effects of QY-54 on the proliferation, invasion, and migration of GBM cells from different species were investigated. At the animal level, the safety of QY-54 in normal mice, its anti-tumor effects in GBM mice, and its effects on cognition protective function were examined.
Results: At the cellular level, QY-54 exhibited significant inhibitory effects on the proliferation, migration, and invasion of GBM cells derived from different species. At the animal level, QY-54 showed low toxicity in normal mice. Moreover, it significantly inhibited GBM tumor growth, promoted tumor cell apoptosis, suppressed neuroinflammation, protected neurons, and improved the general condition and cognitive function of GBM mice. In Western blot experiments, QY-54 upregulated c-jun N-terminal kinase (JNK) levels to exert an inhibitory effect on glioma.
Conclusion: QY-54 exhibits dual effects of anti-glioblastoma and cognitive improvement, by inhibiting BChE and activating the JNK signaling pathway. QY-54 is a highly promising drug for the treatment of glioblastoma with neuroprotective profile.
目的:探讨丁基胆碱酯酶(BChE)抑制剂QY-54是否可用于治疗胶质母细胞瘤(GBM)并发挥神经保护作用。方法:在细胞水平上研究QY-54对不同物种GBM细胞增殖、侵袭和迁移的影响。在动物水平上,观察芪y -54对正常小鼠的安全性、对GBM小鼠的抗肿瘤作用以及对认知保护功能的影响。结果:在细胞水平上,QY-54对不同种类GBM细胞的增殖、迁移和侵袭均有明显的抑制作用。在动物水平上,QY-54对正常小鼠的毒性较低。显著抑制GBM肿瘤生长,促进肿瘤细胞凋亡,抑制神经炎症,保护神经元,改善GBM小鼠一般状况和认知功能。在Western blot实验中,QY-54上调c-jun n -末端激酶(JNK)水平,对胶质瘤发挥抑制作用。结论:QY-54通过抑制BChE和激活JNK信号通路,具有抗胶质母细胞瘤和改善认知的双重作用。QY-54是一种很有前景的治疗胶质母细胞瘤的药物,具有神经保护作用。
期刊介绍:
Future Medicinal Chemistry offers a forum for the rapid publication of original research and critical reviews of the latest milestones in the field. Strong emphasis is placed on ensuring that the journal stimulates awareness of issues that are anticipated to play an increasingly central role in influencing the future direction of pharmaceutical chemistry. Where relevant, contributions are also actively encouraged on areas as diverse as biotechnology, enzymology, green chemistry, genomics, immunology, materials science, neglected diseases and orphan drugs, pharmacogenomics, proteomics and toxicology.