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Metabotropic Glutamate Receptors Type 3 and 5 Feature the "NeuroTransmitter-type" of Glioblastoma: A Bioinformatic Approach.
Caridi, Matteo; Alborghetti, Marika; Pellicelli, Valeria; Orlando, Rosamaria; Pontieri, Francesco Ernesto; Battaglia, Giuseppe; Arcella, Antonietta.
Affiliation
  • Caridi M; Division of Hematology and Clinical Immunology, Department of Medicine, University of Perugia, Perugia, Italy.
  • Alborghetti M; Department of Neuroscience, Mental Health and Sensory Organs, Sapienza University of Rome, Rome, Italy.
  • Pellicelli V; Internal Medicine, Sapienza University of Rome, Rome, Italy.
  • Orlando R; Department of Physiology and Pharmacology, University Sapienza of Roma, Rome, Italy.
  • Pontieri FE; IRCCS Neuromed, Pozzilli, Italy.
  • Battaglia G; Department of Neuroscience, Mental Health and Sensory Organs, Sapienza University of Rome, Rome, Italy.
  • Arcella A; IRCCS Fondazione Santa Lucia, Rome, Italy.
Curr Neuropharmacol ; 22(11): 1923-1939, 2024.
Article in En | MEDLINE | ID: mdl-38509672
ABSTRACT

BACKGROUND:

Glioblastoma (GBM) represents an aggressive and common tumor of the central nervous system. The prognosis of GBM is poor, and despite a refined genetic and molecular characterization, pharmacological treatment is largely suboptimal.

OBJECTIVE:

Contribute to defining a therapeutic line in GBM targeting the mGlu3 receptor in line with the principles of precision medicine.

METHODS:

Here, we performed a computational analysis focused on the expression of type 3 and 5 metabotropic glutamate receptor subtypes (mGlu3 and mGlu5, respectively) in high- and low-grade gliomas.

RESULTS:

The analysis allowed the identification of a particular high-grade glioma type, characterized by a high expression level of both receptor subtypes and by other markers of excitatory and inhibitory neurotransmission. This so-called neurotransmitter-GBM (NT-GBM) also shows a distinct immunological, metabolic, and vascularization gene signature.

CONCLUSION:

Our findings might lay the groundwork for a targeted therapy to be specifically applied to this putative novel type of GBM.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain Neoplasms / Receptors, Metabotropic Glutamate / Glioblastoma / Computational Biology Limits: Humans Language: En Journal: Curr Neuropharmacol / Curr. neuropharmacol / Current neuropharmacology Year: 2024 Document type: Article Affiliation country: Italia Country of publication: Emiratos Árabes Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain Neoplasms / Receptors, Metabotropic Glutamate / Glioblastoma / Computational Biology Limits: Humans Language: En Journal: Curr Neuropharmacol / Curr. neuropharmacol / Current neuropharmacology Year: 2024 Document type: Article Affiliation country: Italia Country of publication: Emiratos Árabes Unidos