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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.

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/11461351/3a744b5861d8/fphar-15-1468920-g001.jpg

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