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毒蕈碱受体药物苯海索可改变间充质胶质母细胞瘤的生长。

Muscarinic receptor drug trihexyphenidyl can alter growth of mesenchymal glioblastoma .

作者信息

Du Renfei, Sanin Ahmed Y, Shi Wenjie, Huang Bing, Nickel Ann-Christin, Vargas-Toscano Andres, Huo Shuran, Nickl-Jockschat Thomas, Dumitru Claudia A, Hu Wei, Duan Siyu, Sandalcioglu I Erol, Croner Roland S, Alcaniz Joshua, Walther Wolfgang, Berndt Carsten, Kahlert Ulf D

机构信息

Chifeng Municipal Hospital, Chifeng, China.

Clinic for Neurosurgery, Medical Faculty and University Hospital Düsseldorf, Heinrich-Heine University, Düsseldorf, Germany.

出版信息

Front Pharmacol. 2024 Sep 25;15:1468920. doi: 10.3389/fphar.2024.1468920. eCollection 2024.

DOI:10.3389/fphar.2024.1468920
PMID:39386028
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11461351/
Abstract

Glioblastoma (GBM) is the most commonly occurring and most aggressive primary brain tumor. Transcriptomics-based tumor subtype classification has established the mesenchymal lineage of GBM (MES-GBM) as cancers with particular aggressive behavior and high levels of therapy resistance. Previously it was show that Trihexyphenidyl (THP), a market approved M1 muscarinic receptor-targeting oral drug can suppress proliferation and survival of GBM stem cells from the classical transcriptomic subtype. In a series of experiments, this study confirms the therapeutic potential of THP, by effectively suppressing the growth, proliferation and survival of MES-GBM cells with limited effects on non-tumor cells. Transcriptomic profiling of treated cancer cells identified genes and associated metabolic signaling pathways as possible underlying molecular mechanisms responsible for THP-induced effects. trials of THP in immunocompromised mice carry orthotopic MES-GBMs showed moderate response to the drug. This study further highlights the potential of THP repurposing as an anti-cancer treatment regimen but mode of action and d optimal treatment procedures for regimens need to be investigated further.

摘要

胶质母细胞瘤(GBM)是最常见且最具侵袭性的原发性脑肿瘤。基于转录组学的肿瘤亚型分类已将GBM的间充质谱系(MES-GBM)确定为具有特别侵袭性行为和高水平治疗抗性的癌症。先前研究表明,已获市场批准的靶向M1毒蕈碱受体的口服药物苯海索(THP)可抑制经典转录组亚型GBM干细胞的增殖和存活。在一系列实验中,本研究通过有效抑制MES-GBM细胞的生长、增殖和存活,且对非肿瘤细胞影响有限,证实了THP的治疗潜力。对经处理癌细胞的转录组分析确定了基因及相关代谢信号通路,它们可能是THP诱导效应的潜在分子机制。在携带原位MES-GBM的免疫缺陷小鼠中进行的THP试验显示该药物有中度反应。本研究进一步突出了将THP重新用作抗癌治疗方案的潜力,但作用方式和该方案的最佳治疗程序仍需进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfcf/11461351/6b54e8809927/fphar-15-1468920-g007.jpg
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本文引用的文献

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Clinically relevant glioblastoma patient-derived xenograft models to guide drug development and identify molecular signatures.用于指导药物研发和识别分子特征的临床相关胶质母细胞瘤患者来源异种移植模型
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Crosstalk between β-Catenin and CCL2 Drives Migration of Monocytes towards Glioblastoma Cells.
β-连环蛋白与 CCL2 之间的串扰驱动单核细胞向神经胶质瘤细胞迁移。
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