Acid-sensing ion channel 3 is a new potential therapeutic target for the control of glioblastoma cancer stem cells growth.
Andrea BalboniCamilla D'AngeloNicoletta ColluraSimone BruscoClaudia Di BerardinoAltea TargaBeatrice MassotiEloise MastrangeloMario MilaniPierfausto SeneciVania BroccoliLuca MuzioRossella GalliAndrea MenegonPublished in: Scientific reports (2024)
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.
Keyphrases
- cancer stem cells
- cell migration
- stem cells
- induced apoptosis
- spinal cord
- endothelial cells
- blood brain barrier
- poor prognosis
- oxidative stress
- papillary thyroid
- signaling pathway
- cell cycle arrest
- squamous cell carcinoma
- induced pluripotent stem cells
- locally advanced
- radiation induced
- cell proliferation
- combination therapy
- cerebrospinal fluid
- brain injury
- bone marrow
- endoplasmic reticulum stress
- spinal cord injury
- cell death
- young adults
- long non coding rna
- radiation therapy