Institute of Laboratory Medicine, School of Medicine, University of Pécs, 7624 Pécs, Hungary.
Szentagothai Research Center, University of Pécs, 7624 Pécs, Hungary.
Cells. 2021 Mar 4;10(3):549. doi: 10.3390/cells10030549.
Glioblastoma (GBM) is the most aggressive tumor of the central nervous system (CNS). The standard of care improves the overall survival of patients only by a few months. Explorations of new therapeutic targets related to molecular properties of the tumor are under way. Even though neurotransmitters and their receptors normally function as mediators of interneuronal communication, growing data suggest that these molecules are also involved in modulating the development and growth of GBM by acting on neuronal and glioblastoma stem cells. In our previous DNA CpG methylation studies, gene ontology analyses revealed the involvement of the monoamine pathway in sequential GBM. In this follow-up study, we quantitated the expression levels of four selected catecholamine pathway markers (alpha 1D adrenergic receptor-ADRA1D; adrenergic beta receptor kinase 1 or G protein-coupled receptor kinase 2-ADRBK1/GRK2; dopamine receptor D2-DRD2; and synaptic vesicle monoamine transporter-SLC18A2) by immunohistochemistry, and compared the histological scores with the methylation levels within the promoters + genes of these markers in 21 pairs of sequential GBM and in controls. Subsequently, we also determined the promoter and gene methylation levels of the same markers in an independent database cohort of sequential GBM pairs. These analyses revealed partial inverse correlations between the catecholamine protein expression and promoter + gene methylation levels, when the tumor and control samples were compared. However, we found no differences in the promoter + gene methylation levels of these markers in either our own or in the database primary-recurrent GBM pairs, despite the higher protein expression of all markers in the primary samples. This observation suggests that regulation of catecholamine expression is only partially related to CpG methylation within the promoter + gene regions, and additional mechanisms may also influence the expression of these markers in progressive GBM. These analyses underscore the involvement of certain catecholamine pathway markers in GBM development and suggest that these molecules mediating or modulating tumor growth merit further exploration.
胶质母细胞瘤(GBM)是中枢神经系统(CNS)中最具侵袭性的肿瘤。标准治疗方法只能使患者的总生存期延长几个月。目前正在探索与肿瘤分子特性相关的新治疗靶点。尽管神经递质及其受体通常作为神经元间通讯的介质发挥作用,但越来越多的数据表明,这些分子还通过作用于神经元和胶质母细胞瘤干细胞来调节 GBM 的发育和生长。在我们之前的 DNA CpG 甲基化研究中,基因本体分析表明单胺途径参与了 GBM 的连续发生。在这项后续研究中,我们通过免疫组织化学定量检测了四个选定儿茶酚胺途径标志物(α 1D 肾上腺素能受体-ADRA1D;肾上腺素能β受体激酶 1 或 G 蛋白偶联受体激酶 2-ADRBK1/GRK2;多巴胺受体 D2-DRD2;和突触小泡单胺转运体-SLC18A2)的表达水平,并将这些标志物的启动子+基因的甲基化水平与 21 对连续 GBM 和对照组织的组织学评分进行了比较。随后,我们还在一个独立的连续 GBM 配对数据库队列中确定了这些标志物的相同标记的启动子和基因甲基化水平。这些分析表明,当比较肿瘤和对照样本时,儿茶酚胺蛋白表达与启动子+基因甲基化水平之间存在部分负相关。然而,我们发现无论是在我们自己的数据库还是在数据库原发性复发性 GBM 配对中,这些标志物的启动子+基因甲基化水平都没有差异,尽管所有标志物在原发性样本中的蛋白表达更高。这一观察结果表明,儿茶酚胺表达的调节仅部分与启动子+基因区域内的 CpG 甲基化有关,并且其他机制也可能影响这些标志物在进行性 GBM 中的表达。这些分析强调了某些儿茶酚胺途径标志物在 GBM 发展中的作用,并表明这些调节或调节肿瘤生长的分子值得进一步探索。