Synergistic action of JNK activation and BChE inhibition: a novel anti- glioblastoma compound with neuroprotective profile.

IF 3.3 4区 医学 Q3 CHEMISTRY, MEDICINAL
Future medicinal chemistry Pub Date : 2026-06-01 Epub Date: 2026-04-15 DOI:10.1080/17568919.2026.2658833
Ziyao Lu, Qinghong Liao, Yuetong Duan, Kaixuan Wang, Siyu He, Weiping Lyu, Xuehong Chen, Qi Li
{"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.

JNK活化和BChE抑制的协同作用:一种具有神经保护作用的新型抗胶质母细胞瘤化合物。
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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Future medicinal chemistry
Future medicinal chemistry CHEMISTRY, MEDICINAL-
CiteScore
5.80
自引率
2.40%
发文量
118
审稿时长
4-8 weeks
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.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书