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人胶质母细胞瘤中新型潜在治疗靶点阿片肽受体及其内源性配体在不同干细胞群体中的表达

Expression of the apelin receptor, a novel potential therapeutic target, and its endogenous ligands in diverse stem cell populations in human glioblastoma.

作者信息

Williams Thomas L, Nwokoye Peter, Kuc Rhoda E, Smith Kieran, Paterson Anna L, Allinson Kieren, Maguire Janet J, Davenport Anthony P

机构信息

Experimental Medicine and Immunotherapeutics, University of Cambridge, Addenbrooke's Hospital, Cambridge, United Kingdom.

Department of Pathology, Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom.

出版信息

Front Neurosci. 2024 May 13;18:1379658. doi: 10.3389/fnins.2024.1379658. eCollection 2024.

Abstract

Glioblastoma multiforme (GBM) is one of the most common and lethal forms of brain cancer, carrying a very poor prognosis (median survival of ~15 months post-diagnosis). Treatment typically involves invasive surgical resection of the tumour mass, followed by radiotherapy and adjuvant chemotherapy using the alkylating agent temozolomide, but over half of patients do not respond to this drug and considerable resistance is observed. Tumour heterogeneity is the main cause of therapeutic failure, where diverse progenitor glioblastoma stem cell (GSC) lineages in the microenvironment drive tumour recurrence and therapeutic resistance. The apelin receptor is a class A GPCR that binds two endogenous peptide ligands, apelin and ELA, and plays a role in the proliferation and survival of cancer cells. Here, we used quantitative whole slide immunofluorescent imaging of human GBM samples to characterise expression of the apelin receptor and both its ligands in the distinct GSC lineages, namely neural-progenitor-like cells (NPCs), oligodendrocyte-progenitor-like cells (OPCs), and mesenchymal-like cells (MES), as well as reactive astrocytic cells. The data confirm the presence of the apelin receptor as a tractable drug target that is common across the key cell populations driving tumour growth and maintenance, offering a potential novel therapeutic approach for patients with GBM.

摘要

多形性胶质母细胞瘤(GBM)是最常见且致命的脑癌形式之一,预后极差(诊断后中位生存期约为15个月)。治疗通常包括对肿瘤块进行侵入性手术切除,随后进行放疗以及使用烷化剂替莫唑胺进行辅助化疗,但超过半数的患者对该药物无反应,且存在明显的耐药性。肿瘤异质性是治疗失败的主要原因,微环境中不同的祖细胞性胶质母细胞瘤干细胞(GSC)谱系驱动肿瘤复发和治疗耐药性。阿片肽受体是一种A类G蛋白偶联受体,它结合两种内源性肽配体,即阿片肽和ELA,并在癌细胞的增殖和存活中发挥作用。在此,我们利用人GBM样本的定量全玻片免疫荧光成像来表征阿片肽受体及其两种配体在不同GSC谱系中的表达,这些谱系包括神经祖细胞样细胞(NPC)、少突胶质细胞祖细胞样细胞(OPC)、间充质样细胞(MES)以及反应性星形细胞。数据证实阿片肽受体作为一个可靶向的药物靶点存在于驱动肿瘤生长和维持的关键细胞群体中,为GBM患者提供了一种潜在的新型治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1997/11128631/79e6387680cb/fnins-18-1379658-g001.jpg

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