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酸敏离子通道 3 是控制神经胶质瘤肿瘤干细胞生长的新的潜在治疗靶点。

Acid-sensing ion channel 3 is a new potential therapeutic target for the control of glioblastoma cancer stem cells growth.

机构信息

Experimental Imaging Centre, San Raffaele Scientific Institute IRCCS, 20132, Milan, Italy.

Division of Neuroscience, San Raffaele Scientific Institute IRCCS, 20132, Milan, Italy.

出版信息

Sci Rep. 2024 Sep 3;14(1):20421. doi: 10.1038/s41598-024-71623-9.

Abstract

Glioblastoma (GBM) is the most common malignant primary brain cancer that, despite recent advances in the understanding of its pathogenesis, remains incurable. GBM contains a subpopulation of cells with stem cell-like properties called cancer stem cells (CSCs). Several studies have demonstrated that CSCs are resistant to conventional chemotherapy and radiation thus representing important targets for novel anti-cancer therapies. Proton sensing receptors expressed by CSCs could represent important factors involved in the adaptation of tumours to the extracellular environment. Accordingly, the expression of acid-sensing ion channels (ASICs), proton-gated sodium channels mainly expressed in the neurons of peripheral (PNS) and central nervous system (CNS), has been demonstrated in several tumours and linked to an increase in cell migration and proliferation. In this paper we report that the ASIC3 isoform, usually absent in the CNS and present in the PNS, is enriched in human GBM CSCs while poorly expressed in the healthy human brain. We propose here a novel therapeutic strategy based on the pharmacological activation of ASIC3, which induces a significant GBM CSCs damage while being non-toxic for neurons. This approach might offer a promising and appealing new translational pathway for the treatment of glioblastoma.

摘要

胶质母细胞瘤(GBM)是最常见的恶性原发性脑癌,尽管近年来对其发病机制的认识有所进展,但仍然无法治愈。GBM 中存在一群具有干细胞样特性的细胞,称为癌症干细胞(CSC)。多项研究表明,CSC 对常规化疗和放疗具有抗性,因此是新型抗癌疗法的重要靶点。CSC 表达的质子感应受体可能是肿瘤适应细胞外环境的重要因素。因此,酸感应离子通道(ASICs)的表达,即主要在外周神经系统(PNS)和中枢神经系统(CNS)神经元中表达的质子门控钠离子通道,已在多种肿瘤中得到证实,并与细胞迁移和增殖增加有关。在本文中,我们报告说,通常不存在于中枢神经系统而存在于周围神经系统中的 ASIC3 同工型在人 GBM CSC 中富集,而在健康人脑组织中表达水平较低。我们在这里提出了一种新的治疗策略,基于 ASIC3 的药理学激活,这会导致 GBM CSCs 明显损伤,而对神经元无毒。这种方法可能为治疗胶质母细胞瘤提供一条有前途和有吸引力的新转化途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4548/11372124/6da3d18deebd/41598_2024_71623_Fig1_HTML.jpg

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