Engineered nanovesicles targeting SERPINE1 overcome temozolomide resistance in glioblastoma

IF 4.4 2区 生物学 Q2 CELL BIOLOGY
Jianping Wen , Dongxu Wu , Yi Le , Zonghua Yin , Minglong Chen , Yulong Shen , Xia Wu , Kebo Liu , Kun Luo , Zhicheng Shu , Qingxia Shu , Dongsheng Ouyang
{"title":"Engineered nanovesicles targeting SERPINE1 overcome temozolomide resistance in glioblastoma","authors":"Jianping Wen ,&nbsp;Dongxu Wu ,&nbsp;Yi Le ,&nbsp;Zonghua Yin ,&nbsp;Minglong Chen ,&nbsp;Yulong Shen ,&nbsp;Xia Wu ,&nbsp;Kebo Liu ,&nbsp;Kun Luo ,&nbsp;Zhicheng Shu ,&nbsp;Qingxia Shu ,&nbsp;Dongsheng Ouyang","doi":"10.1016/j.cellsig.2025.111763","DOIUrl":null,"url":null,"abstract":"<div><div>Glioblastoma multiforme (GBM) is a highly aggressive brain tumor with limited treatment options due to its resistance to temozolomide (TMZ). This study explores a novel therapeutic approach using engineered cell membrane nanovesicles loaded with SERPINE1 inhibitors to combat TMZ resistance. High-throughput sequencing identified pivotal genes associated with resistance, while the nanovesicles demonstrated excellent stability and the ability to cross the blood-brain barrier. Functional assays revealed significant suppression of GBM cell viability, migration, and invasion, accompanied by reduced expression of SERPINE1 and VEGF, suggesting inhibition of angiogenesis and tumor progression. These findings highlight the potential of SERPINE1-targeted nanovesicles as an innovative and effective strategy for overcoming TMZ resistance in GBM.</div></div>","PeriodicalId":9902,"journal":{"name":"Cellular signalling","volume":"132 ","pages":"Article 111763"},"PeriodicalIF":4.4000,"publicationDate":"2025-03-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cellular signalling","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0898656825001767","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Glioblastoma multiforme (GBM) is a highly aggressive brain tumor with limited treatment options due to its resistance to temozolomide (TMZ). This study explores a novel therapeutic approach using engineered cell membrane nanovesicles loaded with SERPINE1 inhibitors to combat TMZ resistance. High-throughput sequencing identified pivotal genes associated with resistance, while the nanovesicles demonstrated excellent stability and the ability to cross the blood-brain barrier. Functional assays revealed significant suppression of GBM cell viability, migration, and invasion, accompanied by reduced expression of SERPINE1 and VEGF, suggesting inhibition of angiogenesis and tumor progression. These findings highlight the potential of SERPINE1-targeted nanovesicles as an innovative and effective strategy for overcoming TMZ resistance in GBM.
靶向SERPINE1的工程纳米囊泡克服了胶质母细胞瘤对替莫唑胺的耐药性。
多形性胶质母细胞瘤(GBM)是一种高度侵袭性的脑肿瘤,由于其对替莫唑胺(TMZ)的耐药性,治疗选择有限。本研究探索了一种新的治疗方法,利用负载SERPINE1抑制剂的工程细胞膜纳米囊泡来对抗TMZ耐药性。高通量测序确定了与耐药性相关的关键基因,而纳米囊泡表现出优异的稳定性和穿越血脑屏障的能力。功能分析显示,其显著抑制GBM细胞活力、迁移和侵袭,并伴有SERPINE1和VEGF的表达降低,表明其抑制了血管生成和肿瘤进展。这些发现突出了serpine1靶向纳米囊泡作为克服GBM中TMZ耐药性的创新和有效策略的潜力。
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
Cellular signalling
Cellular signalling 生物-细胞生物学
CiteScore
8.40
自引率
0.00%
发文量
250
审稿时长
27 days
期刊介绍: Cellular Signalling publishes original research describing fundamental and clinical findings on the mechanisms, actions and structural components of cellular signalling systems in vitro and in vivo. Cellular Signalling aims at full length research papers defining signalling systems ranging from microorganisms to cells, tissues and higher organisms.
×
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:481959085
Book学术官方微信