Modulating voltage-gated sodium channels to enhance differentiation and sensitize glioblastoma cells to chemotherapy

Giammello, Francesca, Biella, Chiara, Priori, Erica Cecilia, Filippo, Matilde Amat Di San, Leone, Roberta, D'Ambrosio, Francesca, Paterno', Martina, Cassioli, Giulia, Minetti, Antea, Macchi, Francesca, Spalletti, Cristina, Morella, Ilaria ORCID: https://orcid.org/0000-0001-5691-5400, Ruberti, Cristina, Tremonti, Beatrice, Barbieri, Federica, Lombardi, Giuseppe, Brambilla, Riccardo ORCID: https://orcid.org/0000-0003-3569-5706, Florio, Tullio, Galli, Rossella, Rossi, Paola and Brandalise, Federico 2024. Modulating voltage-gated sodium channels to enhance differentiation and sensitize glioblastoma cells to chemotherapy. Cell Communication and Signaling 22 , 434. 10.1186/s12964-024-01819-z

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Abstract

Background Glioblastoma (GBM) stands as the most prevalent and aggressive form of adult gliomas. Despite the implementation of intensive therapeutic approaches involving surgery, radiation, and chemotherapy, Glioblastoma Stem Cells contribute to tumor recurrence and poor prognosis. The induction of Glioblastoma Stem Cells differentiation by manipulating the transcriptional machinery has emerged as a promising strategy for GBM treatment. Here, we explored an innovative approach by investigating the role of the depolarized resting membrane potential (RMP) observed in patient-derived GBM sphereforming cell (GSCs), which allows them to maintain a stemness profile when they reside in the G0 phase of the cell cycle. Methods We conducted molecular biology and electrophysiological experiments, both in vitro and in vivo, to examine the functional expression of the voltage-gated sodium channel (Nav) in GSCs, particularly focusing on its cell cycle-dependent functional expression. Nav activity was pharmacologically manipulated, and its effects on GSCs behavior were assessed by live imaging cell cycle analysis, self-renewal assays, and chemosensitivity assays. Mechanistic insights into the role of Nav in regulating GBM stemness were investigated through pathway analysis in vitro and through tumor proliferation assay in vivo. Results We demonstrated that Nav is functionally expressed by GSCs mainly during the G0 phase of the cell cycle, suggesting its pivotal role in modulating the RMP. The pharmacological blockade of Nav made GBM cells more susceptible to temozolomide (TMZ), a standard drug for this type of tumor, by inducing cell cycle re-entry from G0 phase to G1/S transition. Additionally, inhibition of Nav substantially influenced the self-renewal and multipotency features of GSCs, concomitantly enhancing their degree of differentiation. Finally, our data suggested that Nav positively regulates GBM stemness by depolarizing the RMP and suppressing the ERK signaling pathway. Of note, in vivo proliferation assessment confirmed the increased susceptibility to TMZ following pharmacological blockade of Nav. Conclusions This insight positions Nav as a promising prognostic biomarker and therapeutic target for GBM patients, particularly in conjunction with temozolomide treatment.

Item Type:	Article
Date Type:	Published Online
Status:	Published
Schools:	Medicine Biosciences
Publisher:	BioMed Central
ISSN:	1478-811X
Date of First Compliant Deposit:	11 November 2024
Date of Acceptance:	4 September 2024
Last Modified:	15 Nov 2024 11:01
URI:	https://orca.cardiff.ac.uk/id/eprint/173811

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